Covance Jobshttp://jobsearch.covance.com Evansville, IN jobs with Covance(c) 2009, Covance10Sat, 25 Jun 2016 08:51:39 EST1332759Sr 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=1332759Fri, 24 Jun 2016 05:35:32 GMT1332529Associate 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=1332529Thu, 23 Jun 2016 13:09:45 GMT1332128Research Nurse IWe are currently hiring a Clinical Research Nurse for our Clinical Pharmacology site in Evansville, IN. This is a weekend only shift with one rotating weekday. The following qualifications are acceptable: ASN, RN or BSN The Research Nurse will be responsible for study unit activities in the conduct of clinical trials with emphasis on the safety and welfare of study participants. Duties and Resphttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1332128Wed, 22 Jun 2016 16:41:43 GMT1326511Project 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=1326511Tue, 21 Jun 2016 05:46:11 GMT1326444Sr 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=1326444Tue, 21 Jun 2016 05:46:05 GMT1326376Sr 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=1326376Tue, 21 Jun 2016 05:45:42 GMT1325771Sr 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=1325771Fri, 17 Jun 2016 14:57:33 GMT1325631Clinical 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=1325631Fri, 17 Jun 2016 05:29:58 GMT1325563Director 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=1325563Fri, 17 Jun 2016 05:29:53 GMT1325249Client 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=1325249Thu, 16 Jun 2016 14:48:59 GMT1325248Paramedic IIAre you looking for a career change and opportunities for growth? Covance is the place for you! We offer great benefits that begin on day one. Special Factors: MUST be open to the following: - Overtime, rotating shifts, and weekend work as required. The Paramedic is responsible for performing practical/administrative activities of clinical trials in Clinical Pharmacology in line with protocol ahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325248Thu, 16 Jun 2016 14:48:58 GMT1325185Sr 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=1325185Thu, 16 Jun 2016 14:48:52 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 GMT1324552Associate 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=1324552Tue, 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 GMT1324551Associate 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=1324551Tue, 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 GMT1324550Associate 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=1324550Tue, 14 Jun 2016 15:12:59 GMT1324547Associate 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=1324547Tue, 14 Jun 2016 15:12:59 GMT1324548Associate 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=1324548Tue, 14 Jun 2016 15:12:59 GMT1324545Associate 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=1324545Tue, 14 Jun 2016 15:12:59 GMT1324546Associate 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=1324546Tue, 14 Jun 2016 15:12:59 GMT1324543Associate 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=1324543Tue, 14 Jun 2016 15:12:59 GMT1324544Associate 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=1324544Tue, 14 Jun 2016 15:12:59 GMT1324542Associate 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=1324542Tue, 14 Jun 2016 15:12:59 GMT1320785Manager 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=1320785Fri, 27 May 2016 15:46:45 GMT1319241Sr 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=1319241Mon, 23 May 2016 13:06:55 GMT1319016Senior 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=1319016Mon, 23 May 2016 06:17:00 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 GMT1319015Senior 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=1319015Mon, 23 May 2016 06:17:00 GMT1319013Senior 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=1319013Mon, 23 May 2016 06:17:00 GMT1319014Senior 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=1319014Mon, 23 May 2016 06:17:00 GMT1319012Senior 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=1319012Mon, 23 May 2016 06:17:00 GMT1318990Clinical Research Coordinator ICovance is hiring a Clinical Research Coordinator for its Evansville, IN location. Must Have: - Typically 1-2 years of professional work Experience , must include clinical research or related Experience . - Basic knowledge of computer and programs (e.g. Microsoft Word, Excel). - Knowledge of drug development process, ICH Guidelines and GCP. Duties and Responsibilities: * Serve as site lead fhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1318990Mon, 23 May 2016 06:15:50 GMT1317645Quality Assurance Officer III Good Manufacturing Practice GMP The Quality Assurance Officer supports the implementation of the global GMP quality management system, helping to ensure that site specific requirements are addressed locally. The Quality Assurance Officer is located at our Greenfield IN site. As a GMP QA Officer your job duties will include: - Monitors and reports on appropriate site metrics and data trends related to the performance of the sithttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1317645Tue, 17 May 2016 13:02:38 GMT1317130Research Nurse IWe are currently hiring a Clinical Research Nurse for our Clinical Pharmacology site in Evansville, IN. MUST BE WILLING to work a flexible rotating shift, a shift differential incentive will be provided. The following qualifications are acceptable: ASN, RN or BSN The Research Nurse will be responsible for study unit activities in the conduct of clinical trials with emphasis on the safety and whttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1317130Mon, 16 May 2016 12:12:38 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 GMT1313112Seeking 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=1313112Fri, 06 May 2016 06:10:56 GMT1313104Limited 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=1313104Fri, 06 May 2016 06:09:26 GMT1313103Limited 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=1313103Fri, 06 May 2016 06:09:25 GMT1313023Seeking 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=1313023Fri, 06 May 2016 06:08:22 GMT1312942Seeking 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=1312942Fri, 06 May 2016 06:07:27 GMT1312933Clinical Research PhysicianCovance is a leading supplier of drug development services to the biotechnology and pharmaceutical industries. We partner with innovative companies, offering valuable services in all phases of the drug development process as well as analytical and commercial impact services. At Covance our people are committed to advancing health care and bringing new medicines to market sooner. This is an excitinhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1312933Fri, 06 May 2016 06:06:18 GMT1312262Senior 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=1312262Wed, 04 May 2016 14:39:29 GMT1306525Sr 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=1306525Mon, 18 Apr 2016 18:21:56 GMT1303185Sr 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=1303185Wed, 06 Apr 2016 06:33:17 GMT1302025Project 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=1302025Fri, 01 Apr 2016 12:30:34 GMT1291934Drug 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=1291934Thu, 10 Mar 2016 06:11:01 GMT1280099Project 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=1280099Mon, 08 Feb 2016 15:17:55 GMT