Covance Jobshttp://jobsearch.covance.com Florida jobs with Covance(c) 2009, Covance10Sun, 26 Jun 2016 02:56:20 EST1332811Sr Mgr Monitoring Data Flow OptimizationThis role will focus on Covance's Xcellerate Monitoring Solution Development e.g. leading product development, process excellence, internal initiatives. The Senior Manager, Central Monitoring is a key member of the global Risk Based Monitoring Team and has overall responsibility and accountability for the execution and implementation of Risk Based Monitoring activities. The Senior Manager, Centrhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1332811Fri, 24 Jun 2016 05:35:33 GMT1332801Sr Mgr Monitoring Data Flow OptimizationThis role will focus on Covance's Xcellerate Monitoring Solution Development e.g. leading product development, process excellence, internal initiatives. The Senior Manager, Central Monitoring is a key member of the global Risk Based Monitoring Team and has overall responsibility and accountability for the execution and implementation of Risk Based Monitoring activities. The Senior Manager, Centrhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1332801Fri, 24 Jun 2016 05:35:32 GMT1332795Sr Mgr Monitoring Data Flow OptimizationThis role will focus on Covance's Xcellerate Monitoring Solution Development e.g. leading product development, process excellence, internal initiatives. The Senior Manager, Central Monitoring is a key member of the global Risk Based Monitoring Team and has overall responsibility and accountability for the execution and implementation of Risk Based Monitoring activities. The Senior Manager, Centrhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1332795Fri, 24 Jun 2016 05:35:32 GMT1332789Sr Mgr Monitoring Data Flow OptimizationThis role will focus on Covance's Xcellerate Monitoring Solution Development e.g. leading product development, process excellence, internal initiatives. The Senior Manager, Central Monitoring is a key member of the global Risk Based Monitoring Team and has overall responsibility and accountability for the execution and implementation of Risk Based Monitoring activities. The Senior Manager, Centrhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1332789Fri, 24 Jun 2016 05:35:32 GMT1332770Sr Mgr Monitoring Data Flow OptimizationThis role will focus on Covance's Xcellerate Monitoring Solution Development e.g. leading product development, process excellence, internal initiatives. The Senior Manager, Central Monitoring is a key member of the global Risk Based Monitoring Team and has overall responsibility and accountability for the execution and implementation of Risk Based Monitoring activities. The Senior Manager, Centrhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1332770Fri, 24 Jun 2016 05:35:32 GMT1332546Associate Manager Early Clinical DevelopmentAssociate CRA Line Manager, Early Clinical Development Location: Remote/Virtual Covance's Early Clinical Development (ECD) team is seeking an Associate CRA Line Manager. Managing a team of CRAs at Covance can lead you to a more fulfilling future. Here, you'll enrich your Experience , working among the best and brightest in our industry with the knowledge that choosing Covance was one of the best http://jobsearch.covance.com/CustomJobDetail.aspx?id=1332546Thu, 23 Jun 2016 13:09:47 GMT1326563Project Director IIGMThe Infectious Diseases, Inflammation and General Medicine Therapeutic Area (IIGM ) provides global expertise across multiple indications and phases in the drug development continuum. Our portfolio of clinical studies is broad, and includes respiratory indications such as Allergic Asthma, Chronic Obstructive Airways Disease and Pulmonary Fibrosis, a range of Autoimmune Mediated Inflammatory Diseashttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326563Tue, 21 Jun 2016 05:46:12 GMT1326553Project Director IIGMThe Infectious Diseases, Inflammation and General Medicine Therapeutic Area (IIGM ) provides global expertise across multiple indications and phases in the drug development continuum. Our portfolio of clinical studies is broad, and includes respiratory indications such as Allergic Asthma, Chronic Obstructive Airways Disease and Pulmonary Fibrosis, a range of Autoimmune Mediated Inflammatory Diseashttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326553Tue, 21 Jun 2016 05:46:12 GMT1326547Project Director IIGMThe Infectious Diseases, Inflammation and General Medicine Therapeutic Area (IIGM ) provides global expertise across multiple indications and phases in the drug development continuum. Our portfolio of clinical studies is broad, and includes respiratory indications such as Allergic Asthma, Chronic Obstructive Airways Disease and Pulmonary Fibrosis, a range of Autoimmune Mediated Inflammatory Diseashttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326547Tue, 21 Jun 2016 05:46:11 GMT1326541Project Director IIGMThe Infectious Diseases, Inflammation and General Medicine Therapeutic Area (IIGM ) provides global expertise across multiple indications and phases in the drug development continuum. Our portfolio of clinical studies is broad, and includes respiratory indications such as Allergic Asthma, Chronic Obstructive Airways Disease and Pulmonary Fibrosis, a range of Autoimmune Mediated Inflammatory Diseashttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326541Tue, 21 Jun 2016 05:46:11 GMT1326522Project Director IIGMThe Infectious Diseases, Inflammation and General Medicine Therapeutic Area (IIGM ) provides global expertise across multiple indications and phases in the drug development continuum. Our portfolio of clinical studies is broad, and includes respiratory indications such as Allergic Asthma, Chronic Obstructive Airways Disease and Pulmonary Fibrosis, a range of Autoimmune Mediated Inflammatory Diseashttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326522Tue, 21 Jun 2016 05:46:11 GMT1326496Sr Project Manager IIGMThe Infectious Diseases, Inflammation and General Medicine Therapeutic Area (IIGM ) provides global expertise across multiple indications and phases in the drug development continuum. Our portfolio of clinical studies is broad, and includes respiratory indications such as Allergic Asthma, Chronic Obstructive Airways Disease and Pulmonary Fibrosis, a range of Autoimmune Mediated Inflammatory Diseashttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326496Tue, 21 Jun 2016 05:46:08 GMT1326486Sr Project Manager IIGMThe Infectious Diseases, Inflammation and General Medicine Therapeutic Area (IIGM ) provides global expertise across multiple indications and phases in the drug development continuum. Our portfolio of clinical studies is broad, and includes respiratory indications such as Allergic Asthma, Chronic Obstructive Airways Disease and Pulmonary Fibrosis, a range of Autoimmune Mediated Inflammatory Diseashttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326486Tue, 21 Jun 2016 05:46:07 GMT1326480Sr Project Manager IIGMThe Infectious Diseases, Inflammation and General Medicine Therapeutic Area (IIGM ) provides global expertise across multiple indications and phases in the drug development continuum. Our portfolio of clinical studies is broad, and includes respiratory indications such as Allergic Asthma, Chronic Obstructive Airways Disease and Pulmonary Fibrosis, a range of Autoimmune Mediated Inflammatory Diseashttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326480Tue, 21 Jun 2016 05:46:07 GMT1326474Sr Project Manager IIGMThe Infectious Diseases, Inflammation and General Medicine Therapeutic Area (IIGM ) provides global expertise across multiple indications and phases in the drug development continuum. Our portfolio of clinical studies is broad, and includes respiratory indications such as Allergic Asthma, Chronic Obstructive Airways Disease and Pulmonary Fibrosis, a range of Autoimmune Mediated Inflammatory Diseashttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326474Tue, 21 Jun 2016 05:46:07 GMT1326455Sr Project Manager IIGMThe Infectious Diseases, Inflammation and General Medicine Therapeutic Area (IIGM ) provides global expertise across multiple indications and phases in the drug development continuum. Our portfolio of clinical studies is broad, and includes respiratory indications such as Allergic Asthma, Chronic Obstructive Airways Disease and Pulmonary Fibrosis, a range of Autoimmune Mediated Inflammatory Diseashttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326455Tue, 21 Jun 2016 05:46:05 GMT1326428Sr Project Manager CV MERCovance's Cardiovascular, Metabolic, Endocrine and Renal Therapeutic Area (CVMER) is highly unique in its sheer scope and size—with focus areas ranging from extremely rare indications to prevalent disease states. From heart disease to diabetes, and obesity to non-alcoholic fatty liver disease, the experts at Covance are working toward the discovery of the most advanced therapies using stem cells ahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326428Tue, 21 Jun 2016 05:45:42 GMT1326418Sr Project Manager CV MERCovance's Cardiovascular, Metabolic, Endocrine and Renal Therapeutic Area (CVMER) is highly unique in its sheer scope and size—with focus areas ranging from extremely rare indications to prevalent disease states. From heart disease to diabetes, and obesity to non-alcoholic fatty liver disease, the experts at Covance are working toward the discovery of the most advanced therapies using stem cells ahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326418Tue, 21 Jun 2016 05:45:42 GMT1326412Sr Project Manager CV MERCovance's Cardiovascular, Metabolic, Endocrine and Renal Therapeutic Area (CVMER) is highly unique in its sheer scope and size—with focus areas ranging from extremely rare indications to prevalent disease states. From heart disease to diabetes, and obesity to non-alcoholic fatty liver disease, the experts at Covance are working toward the discovery of the most advanced therapies using stem cells ahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326412Tue, 21 Jun 2016 05:45:42 GMT1326406Sr Project Manager CV MERCovance's Cardiovascular, Metabolic, Endocrine and Renal Therapeutic Area (CVMER) is highly unique in its sheer scope and size—with focus areas ranging from extremely rare indications to prevalent disease states. From heart disease to diabetes, and obesity to non-alcoholic fatty liver disease, the experts at Covance are working toward the discovery of the most advanced therapies using stem cells ahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326406Tue, 21 Jun 2016 05:45:42 GMT1326387Sr Project Manager CV MERCovance's Cardiovascular, Metabolic, Endocrine and Renal Therapeutic Area (CVMER) is highly unique in its sheer scope and size—with focus areas ranging from extremely rare indications to prevalent disease states. From heart disease to diabetes, and obesity to non-alcoholic fatty liver disease, the experts at Covance are working toward the discovery of the most advanced therapies using stem cells ahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326387Tue, 21 Jun 2016 05:45:42 GMT1325823Sr Director Project Management ONCSENIOR DIRECTOR ONCOLOGY COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. The Senior Director is an Experience d leader within a Therapeutic area (TA) Center of Excellence, and is expected to leverage that Experience to enable a team to grow a portfolio of innovative and profitable business, and/or oversee thttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325823Fri, 17 Jun 2016 14:57:33 GMT1325813Sr Director Project Management ONCSENIOR DIRECTOR ONCOLOGY COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. The Senior Director is an Experience d leader within a Therapeutic area (TA) Center of Excellence, and is expected to leverage that Experience to enable a team to grow a portfolio of innovative and profitable business, and/or oversee thttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325813Fri, 17 Jun 2016 14:57:33 GMT1325807Sr Director Project Management ONCSENIOR DIRECTOR ONCOLOGY COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. The Senior Director is an Experience d leader within a Therapeutic area (TA) Center of Excellence, and is expected to leverage that Experience to enable a team to grow a portfolio of innovative and profitable business, and/or oversee thttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325807Fri, 17 Jun 2016 14:57:33 GMT1325801Sr Director Project Management ONCSENIOR DIRECTOR ONCOLOGY COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. The Senior Director is an Experience d leader within a Therapeutic area (TA) Center of Excellence, and is expected to leverage that Experience to enable a team to grow a portfolio of innovative and profitable business, and/or oversee thttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325801Fri, 17 Jun 2016 14:57:33 GMT1325782Sr Director Project Management ONCSENIOR DIRECTOR ONCOLOGY COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. The Senior Director is an Experience d leader within a Therapeutic area (TA) Center of Excellence, and is expected to leverage that Experience to enable a team to grow a portfolio of innovative and profitable business, and/or oversee thttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325782Fri, 17 Jun 2016 14:57:33 GMT1325682Clinical Project Manager Sr Project Manager Project DirectorDue to growth, Covance needs Clinical Project Managers for all levels. Do you have CRO and/or pharmaceutical Experience to join our Late Stage Project Management team? The Clinical Project Managers are virtual positions. Covance is offering a $15,000 sign-on bonus for Experience d clinical Project Managers! Covance Clinical Project Managers should have a Bachelor's Degree and 5 years' Experienchttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325682Fri, 17 Jun 2016 05:29:59 GMT1325672Clinical Project Manager Sr Project Manager Project DirectorDue to growth, Covance needs Clinical Project Managers for all levels. Do you have CRO and/or pharmaceutical Experience to join our Late Stage Project Management team? The Clinical Project Managers are virtual positions. Covance is offering a $15,000 sign-on bonus for Experience d clinical Project Managers! Covance Clinical Project Managers should have a Bachelor's Degree and 5 years' Experienchttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325672Fri, 17 Jun 2016 05:29:59 GMT1325666Clinical Project Manager Sr Project Manager Project DirectorDue to growth, Covance needs Clinical Project Managers for all levels. Do you have CRO and/or pharmaceutical Experience to join our Late Stage Project Management team? The Clinical Project Managers are virtual positions. Covance is offering a $15,000 sign-on bonus for Experience d clinical Project Managers! Covance Clinical Project Managers should have a Bachelor's Degree and 5 years' Experienchttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325666Fri, 17 Jun 2016 05:29:59 GMT1325660Clinical Project Manager Sr Project Manager Project DirectorDue to growth, Covance needs Clinical Project Managers for all levels. Do you have CRO and/or pharmaceutical Experience to join our Late Stage Project Management team? The Clinical Project Managers are virtual positions. Covance is offering a $15,000 sign-on bonus for Experience d clinical Project Managers! Covance Clinical Project Managers should have a Bachelor's Degree and 5 years' Experienchttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325660Fri, 17 Jun 2016 05:29:59 GMT1325642Clinical Project Manager Sr Project Manager Project DirectorDue to growth, Covance needs Clinical Project Managers for all levels. Do you have CRO and/or pharmaceutical Experience to join our Late Stage Project Management team? The Clinical Project Managers are virtual positions. Covance is offering a $15,000 sign-on bonus for Experience d clinical Project Managers! Covance Clinical Project Managers should have a Bachelor's Degree and 5 years' Experienchttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325642Fri, 17 Jun 2016 05:29:58 GMT1325614Director Site Activation pre awardThe Project Director oversees and directs international clinical trials in the start up phase. Responsibilities typically include developing and managing budgets, timelines, and quality guidelines for projects, thereby ensuring that expectations are met while identifying and mitigating risks. They also drive documentation for the project, ensuring the accuracy and quality of regulatory data. They http://jobsearch.covance.com/CustomJobDetail.aspx?id=1325614Fri, 17 Jun 2016 05:29:54 GMT1325604Director Site Activation pre awardThe Project Director oversees and directs international clinical trials in the start up phase. Responsibilities typically include developing and managing budgets, timelines, and quality guidelines for projects, thereby ensuring that expectations are met while identifying and mitigating risks. They also drive documentation for the project, ensuring the accuracy and quality of regulatory data. They http://jobsearch.covance.com/CustomJobDetail.aspx?id=1325604Fri, 17 Jun 2016 05:29:54 GMT1325598Director Site Activation pre awardThe Project Director oversees and directs international clinical trials in the start up phase. Responsibilities typically include developing and managing budgets, timelines, and quality guidelines for projects, thereby ensuring that expectations are met while identifying and mitigating risks. They also drive documentation for the project, ensuring the accuracy and quality of regulatory data. They http://jobsearch.covance.com/CustomJobDetail.aspx?id=1325598Fri, 17 Jun 2016 05:29:54 GMT1325592Director Site Activation pre awardThe Project Director oversees and directs international clinical trials in the start up phase. Responsibilities typically include developing and managing budgets, timelines, and quality guidelines for projects, thereby ensuring that expectations are met while identifying and mitigating risks. They also drive documentation for the project, ensuring the accuracy and quality of regulatory data. They http://jobsearch.covance.com/CustomJobDetail.aspx?id=1325592Fri, 17 Jun 2016 05:29:54 GMT1325574Director Site Activation pre awardThe Project Director oversees and directs international clinical trials in the start up phase. Responsibilities typically include developing and managing budgets, timelines, and quality guidelines for projects, thereby ensuring that expectations are met while identifying and mitigating risks. They also drive documentation for the project, ensuring the accuracy and quality of regulatory data. They http://jobsearch.covance.com/CustomJobDetail.aspx?id=1325574Fri, 17 Jun 2016 05:29:53 GMT1325544Sr Manager of Clinical OpsCovance's Early Clinical Development team is seeking a Sr Manager of Clinical Operations! A career at Covance can lead you to a more fulfilling future. Here, you'll enrich your Experience , working among the best and brightest in our industry with the knowledge that choosing Covance was one of the best career decisions you've ever made. - Responsible for appropriate management and resolution of phttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325544Fri, 17 Jun 2016 05:29:32 GMT1325297Experienced Histotechnician Pathology 500 Sign On Bonus and Relocation Offered Research Assistant/Histotechnician - Pathology ***This position is based in Madison, WI. $500 Sign On Bonus and Relocation assistance is available. Covance is seeking a Research Assistant to join the Pathology team in Madison, WI. You should have prior histology and necropsy Experience and may be eligible for a sign on bonus.* Job Duties and Responsibilities: - Performs necropsy and/or histolohttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325297Thu, 16 Jun 2016 14:57:36 GMT1325256Client Services Manager Clinical Pharmacology Any Covance OfficeClient Services Manager - Clinical Pharmacology Remote or Any Covance Office - Manage all aspects of quote, proposal and RFI development for assigned opportunities; adhering to agreed-upon BU-specific and enterprise-wide proposal and pricing processes - Manage opportunities autonomously, establishes clear timelines to meet client requirement, anticipates obstacles and provides solutions - Revihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325256Thu, 16 Jun 2016 14:48:59 GMT1325237Sr Director Project Management CV MERSENIOR DIRECTOR CV/MER (CARDIOVASCULAR, METABOLISM, ENDOCRINAL & RENAL) COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. The Senior Director is an Experience d leader within a Therapeutic area (TA) Center of Excellence, and is expected to leverage that Experience to enable a team to grow a portfolio of innovhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325237Thu, 16 Jun 2016 14:48:55 GMT1325227Sr Director Project Management CV MERSENIOR DIRECTOR CV/MER (CARDIOVASCULAR, METABOLISM, ENDOCRINAL & RENAL) COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. The Senior Director is an Experience d leader within a Therapeutic area (TA) Center of Excellence, and is expected to leverage that Experience to enable a team to grow a portfolio of innovhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325227Thu, 16 Jun 2016 14:48:55 GMT1325221Sr Director Project Management CV MERSENIOR DIRECTOR CV/MER (CARDIOVASCULAR, METABOLISM, ENDOCRINAL & RENAL) COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. The Senior Director is an Experience d leader within a Therapeutic area (TA) Center of Excellence, and is expected to leverage that Experience to enable a team to grow a portfolio of innovhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325221Thu, 16 Jun 2016 14:48:55 GMT1325215Sr Director Project Management CV MERSENIOR DIRECTOR CV/MER (CARDIOVASCULAR, METABOLISM, ENDOCRINAL & RENAL) COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. The Senior Director is an Experience d leader within a Therapeutic area (TA) Center of Excellence, and is expected to leverage that Experience to enable a team to grow a portfolio of innovhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325215Thu, 16 Jun 2016 14:48:54 GMT1325196Sr Director Project Management CV MERSENIOR DIRECTOR CV/MER (CARDIOVASCULAR, METABOLISM, ENDOCRINAL & RENAL) COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. The Senior Director is an Experience d leader within a Therapeutic area (TA) Center of Excellence, and is expected to leverage that Experience to enable a team to grow a portfolio of innovhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325196Thu, 16 Jun 2016 14:48:53 GMT1324554Associate Scientific DirectorThe Associate Scientific Director will support commercial, operational and biometrics teams for Global Clinical Pharmacology (GCP), providing input into study design, acting as GCP representative on molecule development teams and performing scientific review of biometrics deliverables. This position must be located at one of our facilities in: Dallas, TX, Evansville, IN or Madison, WI. Re-locatiohttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1324554Tue, 14 Jun 2016 15:12:59 GMT1324555Associate Scientific DirectorThe Associate Scientific Director will support commercial, operational and biometrics teams for Global Clinical Pharmacology (GCP), providing input into study design, acting as GCP representative on molecule development teams and performing scientific review of biometrics deliverables. This position must be located at one of our facilities in: Dallas, TX, Evansville, IN or Madison, WI. Re-locatiohttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1324555Tue, 14 Jun 2016 15:12:59 GMT1324553Associate Scientific DirectorThe Associate Scientific Director will support commercial, operational and biometrics teams for Global Clinical Pharmacology (GCP), providing input into study design, acting as GCP representative on molecule development teams and performing scientific review of biometrics deliverables. This position must be located at one of our facilities in: Dallas, TX, Evansville, IN or Madison, WI. Re-locatiohttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1324553Tue, 14 Jun 2016 15:12:59 GMT1324549Associate Scientific DirectorThe Associate Scientific Director will support commercial, operational and biometrics teams for Global Clinical Pharmacology (GCP), providing input into study design, acting as GCP representative on molecule development teams and performing scientific review of biometrics deliverables. This position must be located at one of our facilities in: Dallas, TX, Evansville, IN or Madison, WI. Re-locatiohttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1324549Tue, 14 Jun 2016 15:12:59 GMT1323744Clinical Research Associate I CRA Monitoring Excellence Academy MEA Research Coordinators and Nurses NeededClinical Research Associate I – Monitoring Excellence Academy Location: Remote/Home Based Are you an Experience d Research Nurse or Study Coordinator? Join the Covance Monitoring Excellence Academy (MEA) and train to be a CRA. If you bring the therapeutic expertise, we will train you to be a top notch CRA. You'll be hired into a full time CRA I position, the first 3-6 months of which will providehttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1323744Fri, 10 Jun 2016 12:38:27 GMT1323734Clinical Research Associate I CRA Monitoring Excellence Academy MEA Research Coordinators and Nurses NeededClinical Research Associate I – Monitoring Excellence Academy Location: Remote/Home Based Are you an Experience d Research Nurse or Study Coordinator? Join the Covance Monitoring Excellence Academy (MEA) and train to be a CRA. If you bring the therapeutic expertise, we will train you to be a top notch CRA. You'll be hired into a full time CRA I position, the first 3-6 months of which will providehttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1323734Fri, 10 Jun 2016 12:38:27 GMT1323728Clinical Research Associate I CRA Monitoring Excellence Academy MEA Research Coordinators and Nurses NeededClinical Research Associate I – Monitoring Excellence Academy Location: Remote/Home Based Are you an Experience d Research Nurse or Study Coordinator? Join the Covance Monitoring Excellence Academy (MEA) and train to be a CRA. If you bring the therapeutic expertise, we will train you to be a top notch CRA. You'll be hired into a full time CRA I position, the first 3-6 months of which will providehttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1323728Fri, 10 Jun 2016 12:38:27 GMT1323724Clinical Research Associate I CRA Monitoring Excellence Academy MEA Research Coordinators and Nurses NeededClinical Research Associate I – Monitoring Excellence Academy Location: Remote/Home Based Are you an Experience d Research Nurse or Study Coordinator? Join the Covance Monitoring Excellence Academy (MEA) and train to be a CRA. If you bring the therapeutic expertise, we will train you to be a top notch CRA. You'll be hired into a full time CRA I position, the first 3-6 months of which will providehttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1323724Fri, 10 Jun 2016 12:38:27 GMT1322364Clinical QC LiaisonResponsible for ensuring that all practical aspects of clinical studies are conducted to the highest possible quality and in accordance with the protocol, SOPs and ICH/GCP standards. Provides leadership, training, coaching and mentoring for study staff. To be involved in all aspects of the capture and review of data generated in studies performed at the Clinic. Proactively drives improvement in thttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1322364Mon, 06 Jun 2016 05:42:02 GMT1322135Clinical Operations Supervisor ICovance is hiring a Clinical Operations Supervisor for it's Daytona Beach facility! Responsible for ensuring that all practical aspects of clinical studies are conducted to the highest possible quality and in accordance with the protocol, SOPs and ICH/GCP standards. Provides leadership, training, coaching and mentoring for study staff. Responsibilities/Duties: - Directly supervises staff whichhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1322135Fri, 03 Jun 2016 18:29:34 GMT1321436Quality Assurance QA Senior LiaisonThe Quality Assurance (QA) Senior Liaison hosts client audits and interacts with Health Authority inspectors to represent Covance. This role will be based at our Daytona Beach, FL facility. ***GCP expereince highly preferred. Responsibilities/Duties Include: - Coordinates preparations for, and participates in regulatory inspections when requested. - Act as an expert on broad based routine (dayhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1321436Wed, 01 Jun 2016 12:34:30 GMT1320789Manager Regulatory Compliance PolicyManager, Regulatory Compliance Policy Location: Remote/Virtual in the US or Europe. Must be able to come into the office periodically. Covance is seeking a process Manager for the Regulatory Compliance Policy team. In this role you will drive, support and implement new company initiatives to help achieve the department's goals, using the vision as a reference point in conducting day-to-day activihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1320789Fri, 27 May 2016 15:46:45 GMT1320557Senior Medical Writer ICovance is seeking a Senior Medical Writer to join our Global Medical Writing team. The Senior Medical Writer must have Experience in clinical trials documentation. The Sr. Medical Writer is a remote position. The Global Medical Writing department is responsible for ensuring that work undertaken meets the requirements of government regulatory agencies locally and worldwide. This responsibility http://jobsearch.covance.com/CustomJobDetail.aspx?id=1320557Thu, 26 May 2016 15:12:18 GMT1320538Senior Medical Writer ICovance is seeking a Senior Medical Writer to join our Global Medical Writing team. The Senior Medical Writer must have Experience in clinical trials documentation. The Sr. Medical Writer is a remote position. The Global Medical Writing department is responsible for ensuring that work undertaken meets the requirements of government regulatory agencies locally and worldwide. This responsibility http://jobsearch.covance.com/CustomJobDetail.aspx?id=1320538Thu, 26 May 2016 15:12:18 GMT1320500ParamedicCovance is recruiting for a Paramedic at its Clinical Research Site in Daytona Beach FL. ***Flexible schedules are required. Responsible for performing practical/administrative activities of clinical trials in Clinical Pharmacology in line with protocol and regulatory requirements. Responsibilities/Duties * Accurate and timely collection of blood samples via venipuncture * Laboratory processinhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1320500Thu, 26 May 2016 15:08:25 GMT1319293Sr QA Auditor ISenior Auditor I Location: Virtual/Remote Travel: Up to 30% Covance is looking for a Senior Auditor to join the Regulatory team. This person will have Experience with TMF audit and auditing in a GCP environment. Responsibilities: - Conducts complex, directed, and/or time sensitive QA audits - Provides suitable recommendations for audit observations; ensures auditees deliver appropriate CAPAs anhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1319293Mon, 23 May 2016 13:06:56 GMT1319283Sr QA Auditor ISenior Auditor I Location: Virtual/Remote Travel: Up to 30% Covance is looking for a Senior Auditor to join the Regulatory team. This person will have Experience with TMF audit and auditing in a GCP environment. Responsibilities: - Conducts complex, directed, and/or time sensitive QA audits - Provides suitable recommendations for audit observations; ensures auditees deliver appropriate CAPAs anhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1319283Mon, 23 May 2016 13:06:55 GMT1319277Sr QA Auditor ISenior Auditor I Location: Virtual/Remote Travel: Up to 30% Covance is looking for a Senior Auditor to join the Regulatory team. This person will have Experience with TMF audit and auditing in a GCP environment. Responsibilities: - Conducts complex, directed, and/or time sensitive QA audits - Provides suitable recommendations for audit observations; ensures auditees deliver appropriate CAPAs anhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1319277Mon, 23 May 2016 13:06:55 GMT1319271Sr QA Auditor ISenior Auditor I Location: Virtual/Remote Travel: Up to 30% Covance is looking for a Senior Auditor to join the Regulatory team. This person will have Experience with TMF audit and auditing in a GCP environment. Responsibilities: - Conducts complex, directed, and/or time sensitive QA audits - Provides suitable recommendations for audit observations; ensures auditees deliver appropriate CAPAs anhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1319271Mon, 23 May 2016 13:06:55 GMT1319252Sr QA Auditor ISenior Auditor I Location: Virtual/Remote Travel: Up to 30% Covance is looking for a Senior Auditor to join the Regulatory team. This person will have Experience with TMF audit and auditing in a GCP environment. Responsibilities: - Conducts complex, directed, and/or time sensitive QA audits - Provides suitable recommendations for audit observations; ensures auditees deliver appropriate CAPAs anhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1319252Mon, 23 May 2016 13:06:55 GMT1319017Senior System AdministratorThe System Administrator will partner with management, operational and QA staff to analyze, implement, advice and support global Clinical Pharmacology electronic data collection and reporting. This position can be based in either: Dallas, TX; Daytona Beach, FL; Evansville, IN; Madison, WI or Nashville, TN. Responsibilities and Duties: - Understands business processes and priorities. Leads evaluahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1319017Mon, 23 May 2016 06:17:00 GMT1317027Associate Start Up Manager Early ClinicalStart Up Associate Project Manager for Early Clinical Development Remote based position, openings nationwide Typically under the direction of the Project Manager/Sr. Project Manager/Project Director, the Associate Project Manager, Study Start Up oversees and manages the study start up phase of regional clinical trials. Responsibilities typically include contributing to the development and managehttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1317027Mon, 16 May 2016 05:57:20 GMT1314934Limited Travel Clinical Research Associate CRA up to 15K sign on Remote/Home Based opportunities available near Dallas, TX and Evansville, IN and Daytona Beach, FL. These are limited travel roles! Covance is looking for Experience d Clinical Research Associate (CRA) to monitor at our Phase I clinical research units.. This is a field based role, but the bulk of sites you'd be visiting are at the unit or in the surrounding area. This is an ideal position for a Chttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1314934Mon, 09 May 2016 12:48:54 GMT1314935Limited Travel Clinical Research Associate CRA up to 15K sign on Remote/Home Based opportunities available near Dallas, TX and Evansville, IN and Daytona Beach, FL. These are limited travel roles! Covance is looking for Experience d Clinical Research Associate (CRA) to monitor at our Phase I clinical research units.. This is a field based role, but the bulk of sites you'd be visiting are at the unit or in the surrounding area. This is an ideal position for a Chttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1314935Mon, 09 May 2016 12:48:54 GMT1313166Seeking CRAs with 6 months 2 years of experience up to 15K Sign on Bonus Seeking Remote Clinical Research Associates Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Inhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1313166Fri, 06 May 2016 06:10:57 GMT1313156Seeking CRAs with 6 months 2 years of experience up to 15K Sign on Bonus Seeking Remote Clinical Research Associates Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Inhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1313156Fri, 06 May 2016 06:10:56 GMT1313150Seeking CRAs with 6 months 2 years of experience up to 15K Sign on Bonus Seeking Remote Clinical Research Associates Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Inhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1313150Fri, 06 May 2016 06:10:56 GMT1313144Seeking CRAs with 6 months 2 years of experience up to 15K Sign on Bonus Seeking Remote Clinical Research Associates Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Inhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1313144Fri, 06 May 2016 06:10:56 GMT1313124Seeking CRAs with 6 months 2 years of experience up to 15K Sign on Bonus Seeking Remote Clinical Research Associates Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Inhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1313124Fri, 06 May 2016 06:10:56 GMT1313077Seeking CRAs with 2 4 years of monitoring experience up to 15K Sign on Bonus Seeking Remote Clinical Research Associates Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Inhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1313077Fri, 06 May 2016 06:08:22 GMT1313067Seeking CRAs with 2 4 years of monitoring experience up to 15K Sign on Bonus Seeking Remote Clinical Research Associates Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Inhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1313067Fri, 06 May 2016 06:08:22 GMT1313061Seeking CRAs with 2 4 years of monitoring experience up to 15K Sign on Bonus Seeking Remote Clinical Research Associates Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Inhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1313061Fri, 06 May 2016 06:08:22 GMT1313055Seeking CRAs with 2 4 years of monitoring experience up to 15K Sign on Bonus Seeking Remote Clinical Research Associates Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Inhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1313055Fri, 06 May 2016 06:08:22 GMT1313035Seeking CRAs with 2 4 years of monitoring experience up to 15K Sign on Bonus Seeking Remote Clinical Research Associates Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Inhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1313035Fri, 06 May 2016 06:08:22 GMT1312996Seeking Senior CRAs 4 years of monitoring experience up to 15K Sign on Bonus Seeking Remote Clinical Research Associates Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Inhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1312996Fri, 06 May 2016 06:07:28 GMT1312986Seeking Senior CRAs 4 years of monitoring experience up to 15K Sign on Bonus Seeking Remote Clinical Research Associates Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Inhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1312986Fri, 06 May 2016 06:07:28 GMT1312980Seeking Senior CRAs 4 years of monitoring experience up to 15K Sign on Bonus Seeking Remote Clinical Research Associates Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Inhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1312980Fri, 06 May 2016 06:07:27 GMT1312974Seeking Senior CRAs 4 years of monitoring experience up to 15K Sign on Bonus Seeking Remote Clinical Research Associates Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Inhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1312974Fri, 06 May 2016 06:07:27 GMT1312954Seeking Senior CRAs 4 years of monitoring experience up to 15K Sign on Bonus Seeking Remote Clinical Research Associates Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Inhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1312954Fri, 06 May 2016 06:07:27 GMT1312277Senior Site Management AssociateCovance is hiring a Senior Site Management Associate to be remotely based within the US. Responsibilities / Duties: *Provide training and direction to the study team regarding adherence to Covance Standard Operating Procedures (SOPs), Project-specific Controlled Documents, FDA and ICH Guidelines, GPPs, and GCPs *Oversee the development and maintenance of tracking systems for projects *Conduct http://jobsearch.covance.com/CustomJobDetail.aspx?id=1312277Wed, 04 May 2016 14:39:29 GMT1312267Senior Site Management AssociateCovance is hiring a Senior Site Management Associate to be remotely based within the US. Responsibilities / Duties: *Provide training and direction to the study team regarding adherence to Covance Standard Operating Procedures (SOPs), Project-specific Controlled Documents, FDA and ICH Guidelines, GPPs, and GCPs *Oversee the development and maintenance of tracking systems for projects *Conduct http://jobsearch.covance.com/CustomJobDetail.aspx?id=1312267Wed, 04 May 2016 14:39:29 GMT1306567Sr Director Operational Strategy and PlanningThe Sr. Director of Strategy and Planning will use an evidence-based approach, work with relevant business development staff and operational leaders to design innovative, but practical and fiscally responsible strategies for inclusion in relevant business development documents and for use in the successful implementation and conduct of clinical trial programs for clients. The Sr. Director of Strahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1306567Mon, 18 Apr 2016 18:21:57 GMT1306561Sr Director Operational Strategy and PlanningThe Sr. Director of Strategy and Planning will use an evidence-based approach, work with relevant business development staff and operational leaders to design innovative, but practical and fiscally responsible strategies for inclusion in relevant business development documents and for use in the successful implementation and conduct of clinical trial programs for clients. The Sr. Director of Strahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1306561Mon, 18 Apr 2016 18:21:57 GMT1306555Sr Director Operational Strategy and PlanningThe Sr. Director of Strategy and Planning will use an evidence-based approach, work with relevant business development staff and operational leaders to design innovative, but practical and fiscally responsible strategies for inclusion in relevant business development documents and for use in the successful implementation and conduct of clinical trial programs for clients. The Sr. Director of Strahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1306555Mon, 18 Apr 2016 18:21:57 GMT1306537Sr Director Operational Strategy and PlanningThe Sr. Director of Strategy and Planning will use an evidence-based approach, work with relevant business development staff and operational leaders to design innovative, but practical and fiscally responsible strategies for inclusion in relevant business development documents and for use in the successful implementation and conduct of clinical trial programs for clients. The Sr. Director of Strahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1306537Mon, 18 Apr 2016 18:21:56 GMT1305782Clinical Team LeadCovance is currently seeking a Clinical Team Lead (CTL) NATIONWIDE to function as the leader for the clinical team in our Clinical Operations Phase II-IV group. Up to 5K sign on bonus for Experience d, qualified CTL candidates The Clinical Team Lead (CTL) is the leader for the clinical team in our Clinical Operations Phase II-IV group. The Clinical Team Lead is a member of the Core Project Team http://jobsearch.covance.com/CustomJobDetail.aspx?id=1305782Thu, 14 Apr 2016 12:55:33 GMT1303237Sr Director Investigative RelationsCovance needs a Senior Director, Investigator Relations who will be a senior leader in our team, to represent our vision, mission, and capabilities in an accurate, compelling and effective manner across all internal stakeholder groups and to clients as assigned for direct engagement, RFP and RFI responses and bid defenses. Remote / virtual opportunity. Education/Qualifications University degree (http://jobsearch.covance.com/CustomJobDetail.aspx?id=1303237Wed, 06 Apr 2016 06:33:17 GMT1303227Sr Director Investigative RelationsCovance needs a Senior Director, Investigator Relations who will be a senior leader in our team, to represent our vision, mission, and capabilities in an accurate, compelling and effective manner across all internal stakeholder groups and to clients as assigned for direct engagement, RFP and RFI responses and bid defenses. Remote / virtual opportunity. Education/Qualifications University degree (http://jobsearch.covance.com/CustomJobDetail.aspx?id=1303227Wed, 06 Apr 2016 06:33:17 GMT1303221Sr Director Investigative RelationsCovance needs a Senior Director, Investigator Relations who will be a senior leader in our team, to represent our vision, mission, and capabilities in an accurate, compelling and effective manner across all internal stakeholder groups and to clients as assigned for direct engagement, RFP and RFI responses and bid defenses. Remote / virtual opportunity. Education/Qualifications University degree (http://jobsearch.covance.com/CustomJobDetail.aspx?id=1303221Wed, 06 Apr 2016 06:33:17 GMT1303215Sr Director Investigative RelationsCovance needs a Senior Director, Investigator Relations who will be a senior leader in our team, to represent our vision, mission, and capabilities in an accurate, compelling and effective manner across all internal stakeholder groups and to clients as assigned for direct engagement, RFP and RFI responses and bid defenses. Remote / virtual opportunity. Education/Qualifications University degree (http://jobsearch.covance.com/CustomJobDetail.aspx?id=1303215Wed, 06 Apr 2016 06:33:17 GMT1303196Sr Director Investigative RelationsCovance needs a Senior Director, Investigator Relations who will be a senior leader in our team, to represent our vision, mission, and capabilities in an accurate, compelling and effective manner across all internal stakeholder groups and to clients as assigned for direct engagement, RFP and RFI responses and bid defenses. Remote / virtual opportunity. Education/Qualifications University degree (http://jobsearch.covance.com/CustomJobDetail.aspx?id=1303196Wed, 06 Apr 2016 06:33:17 GMT1302063Project DirectorCovance is one of the world's largest, most well regarded contract research organizations. We have an exciting opportunity available to join our Early Clinical Development team. The Project Director will oversees and directs multiple clinical trials concurrently. Responsibilities typically include developing and managing budgets, timelines, and quality guidelines for projects, thereby ensuring thhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1302063Fri, 01 Apr 2016 12:30:35 GMT1302054Project DirectorCovance is one of the world's largest, most well regarded contract research organizations. We have an exciting opportunity available to join our Early Clinical Development team. The Project Director will oversees and directs multiple clinical trials concurrently. Responsibilities typically include developing and managing budgets, timelines, and quality guidelines for projects, thereby ensuring thhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1302054Fri, 01 Apr 2016 12:30:34 GMT1302049Project DirectorCovance is one of the world's largest, most well regarded contract research organizations. We have an exciting opportunity available to join our Early Clinical Development team. The Project Director will oversees and directs multiple clinical trials concurrently. Responsibilities typically include developing and managing budgets, timelines, and quality guidelines for projects, thereby ensuring thhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1302049Fri, 01 Apr 2016 12:30:34 GMT1302033Project DirectorCovance is one of the world's largest, most well regarded contract research organizations. We have an exciting opportunity available to join our Early Clinical Development team. The Project Director will oversees and directs multiple clinical trials concurrently. Responsibilities typically include developing and managing budgets, timelines, and quality guidelines for projects, thereby ensuring thhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1302033Fri, 01 Apr 2016 12:30:34 GMT1291986Drug Safety Project ManagerThe Drug Safety Project Manager will: - Manage ‘Client' or ‘Project' specific PV&DSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports) for specified projects. - Manage and process expeditable adverse events to the required standard and submit themhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1291986Thu, 10 Mar 2016 06:11:04 GMT1291976Drug Safety Project ManagerThe Drug Safety Project Manager will: - Manage ‘Client' or ‘Project' specific PV&DSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports) for specified projects. - Manage and process expeditable adverse events to the required standard and submit themhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1291976Thu, 10 Mar 2016 06:11:04 GMT1291970Drug Safety Project ManagerThe Drug Safety Project Manager will: - Manage ‘Client' or ‘Project' specific PV&DSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports) for specified projects. - Manage and process expeditable adverse events to the required standard and submit themhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1291970Thu, 10 Mar 2016 06:11:04 GMT1291964Drug Safety Project ManagerThe Drug Safety Project Manager will: - Manage ‘Client' or ‘Project' specific PV&DSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports) for specified projects. - Manage and process expeditable adverse events to the required standard and submit themhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1291964Thu, 10 Mar 2016 06:11:04 GMT1291945Drug Safety Project ManagerThe Drug Safety Project Manager will: - Manage ‘Client' or ‘Project' specific PV&DSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports) for specified projects. - Manage and process expeditable adverse events to the required standard and submit themhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1291945Thu, 10 Mar 2016 06:11:02 GMT1280147Project DirectorCOVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. We are currently recruiting for a Project Director that will lead a core project team and facilitate team's ability to lead extended/complete relevant studies. This role is a permanent, full-time position that can be either office or home based in a European couhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1280147Mon, 08 Feb 2016 15:17:56 GMT1280138Project DirectorCOVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. We are currently recruiting for a Project Director that will lead a core project team and facilitate team's ability to lead extended/complete relevant studies. This role is a permanent, full-time position that can be either office or home based in a European couhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1280138Mon, 08 Feb 2016 15:17:56 GMT1280127Project DirectorCOVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. We are currently recruiting for a Project Director that will lead a core project team and facilitate team's ability to lead extended/complete relevant studies. This role is a permanent, full-time position that can be either office or home based in a European couhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1280127Mon, 08 Feb 2016 15:17:56 GMT1280109Project DirectorCOVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. We are currently recruiting for a Project Director that will lead a core project team and facilitate team's ability to lead extended/complete relevant studies. This role is a permanent, full-time position that can be either office or home based in a European couhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1280109Mon, 08 Feb 2016 15:17:56 GMT