Covance Jobshttp://jobsearch.covance.com Florida jobs with Covance(c) 2009, Covance10Wed, 27 Jul 2016 01:37:52 EST1339822Associate Start Up Manager Early ClinicalAssociate Start Up 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. - Participate in the planning, management, and sharing of regional site start-up actihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1339822Thu, 21 Jul 2016 13:16:12 GMT1339661Senior Manager Client Proposals Clinical Trial ServicesSenior Manager Client Proposals for Late Phase Clinical Trial Services Remote Home Based Working Option for highly Experience d candidates Working with a global team you will be a vibrant, self-motivated, process driven self-starter, possessing proven ability to deliver in a fast paced, high volume environment, working on both new and existing business opportunities. The primary remit of the rolhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1339661Thu, 21 Jul 2016 05:59:16 GMT1339654Senior Manager Client Proposals Clinical Trial ServicesSenior Manager Client Proposals for Late Phase Clinical Trial Services Remote Home Based Working Option for highly Experience d candidates Working with a global team you will be a vibrant, self-motivated, process driven self-starter, possessing proven ability to deliver in a fast paced, high volume environment, working on both new and existing business opportunities. The primary remit of the rolhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1339654Thu, 21 Jul 2016 05:59:14 GMT1339648Senior Manager Client Proposals Clinical Trial ServicesSenior Manager Client Proposals for Late Phase Clinical Trial Services Remote Home Based Working Option for highly Experience d candidates Working with a global team you will be a vibrant, self-motivated, process driven self-starter, possessing proven ability to deliver in a fast paced, high volume environment, working on both new and existing business opportunities. The primary remit of the rolhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1339648Thu, 21 Jul 2016 05:59:14 GMT1339642Senior Manager Client Proposals Clinical Trial ServicesSenior Manager Client Proposals for Late Phase Clinical Trial Services Remote Home Based Working Option for highly Experience d candidates Working with a global team you will be a vibrant, self-motivated, process driven self-starter, possessing proven ability to deliver in a fast paced, high volume environment, working on both new and existing business opportunities. The primary remit of the rolhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1339642Thu, 21 Jul 2016 05:59:14 GMT1339628Senior Manager Client Proposals Clinical Trial ServicesSenior Manager Client Proposals for Late Phase Clinical Trial Services Remote Home Based Working Option for highly Experience d candidates Working with a global team you will be a vibrant, self-motivated, process driven self-starter, possessing proven ability to deliver in a fast paced, high volume environment, working on both new and existing business opportunities. The primary remit of the rolhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1339628Thu, 21 Jul 2016 05:59:14 GMT1339203Start Up Associate Project Manager ECDStart 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=1339203Tue, 19 Jul 2016 12:39:03 GMT1339187Associate Start Up Manager Early ClinicalAssociate Start Up 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. - Participate in the planning, management, and sharing of regional site start-up actihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1339187Tue, 19 Jul 2016 12:38:05 GMT1338843Manager Investigator Health System RelationshipsThe Manager, Investigator & Health System Relationships is responsible for improving aspects of site identification and study performance by developing and maintaining highly effective relationships with our research partners. This includes understanding and driving innovations that are either envisioned from within Covance or are proposed by our research and channel partners. This role is responshttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1338843Mon, 18 Jul 2016 12:45:35 GMT1338833Manager Investigator Health System RelationshipsThe Manager, Investigator & Health System Relationships is responsible for improving aspects of site identification and study performance by developing and maintaining highly effective relationships with our research partners. This includes understanding and driving innovations that are either envisioned from within Covance or are proposed by our research and channel partners. This role is responshttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1338833Mon, 18 Jul 2016 12:45:35 GMT1338827Manager Investigator Health System RelationshipsThe Manager, Investigator & Health System Relationships is responsible for improving aspects of site identification and study performance by developing and maintaining highly effective relationships with our research partners. This includes understanding and driving innovations that are either envisioned from within Covance or are proposed by our research and channel partners. This role is responshttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1338827Mon, 18 Jul 2016 12:45:35 GMT1338821Manager Investigator Health System RelationshipsThe Manager, Investigator & Health System Relationships is responsible for improving aspects of site identification and study performance by developing and maintaining highly effective relationships with our research partners. This includes understanding and driving innovations that are either envisioned from within Covance or are proposed by our research and channel partners. This role is responshttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1338821Mon, 18 Jul 2016 12:45:35 GMT1338802Manager Investigator Health System RelationshipsThe Manager, Investigator & Health System Relationships is responsible for improving aspects of site identification and study performance by developing and maintaining highly effective relationships with our research partners. This includes understanding and driving innovations that are either envisioned from within Covance or are proposed by our research and channel partners. This role is responshttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1338802Mon, 18 Jul 2016 12:45:35 GMT1338774Project Mgr Regulatory AffairsGlobal Regulatory Affairs (GRA) is responsible for ensuring the quality of documents and submissions to regulatory authorities globally in support of both investigational and marketed product activities. GRA is also responsible for authoring medical & regulatory documents and providing strategic input for projects as required. The Project Manager, Regulatory Affairs is responsible for the managemhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1338774Mon, 18 Jul 2016 12:45:25 GMT1338764Project Mgr Regulatory AffairsGlobal Regulatory Affairs (GRA) is responsible for ensuring the quality of documents and submissions to regulatory authorities globally in support of both investigational and marketed product activities. GRA is also responsible for authoring medical & regulatory documents and providing strategic input for projects as required. The Project Manager, Regulatory Affairs is responsible for the managemhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1338764Mon, 18 Jul 2016 12:45:24 GMT1338758Project Mgr Regulatory AffairsGlobal Regulatory Affairs (GRA) is responsible for ensuring the quality of documents and submissions to regulatory authorities globally in support of both investigational and marketed product activities. GRA is also responsible for authoring medical & regulatory documents and providing strategic input for projects as required. The Project Manager, Regulatory Affairs is responsible for the managemhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1338758Mon, 18 Jul 2016 12:45:24 GMT1338752Project Mgr Regulatory AffairsGlobal Regulatory Affairs (GRA) is responsible for ensuring the quality of documents and submissions to regulatory authorities globally in support of both investigational and marketed product activities. GRA is also responsible for authoring medical & regulatory documents and providing strategic input for projects as required. The Project Manager, Regulatory Affairs is responsible for the managemhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1338752Mon, 18 Jul 2016 12:45:24 GMT1338733Project Mgr Regulatory AffairsGlobal Regulatory Affairs (GRA) is responsible for ensuring the quality of documents and submissions to regulatory authorities globally in support of both investigational and marketed product activities. GRA is also responsible for authoring medical & regulatory documents and providing strategic input for projects as required. The Project Manager, Regulatory Affairs is responsible for the managemhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1338733Mon, 18 Jul 2016 12:45:24 GMT1338197Sr QA Auditor I eTMF Audit Experience NeededSenior 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=1338197Thu, 14 Jul 2016 14:16:27 GMT1338193Sr QA Auditor I eTMF Audit Experience NeededSenior 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=1338193Thu, 14 Jul 2016 14:16:27 GMT1336381Sr Associate CDS Clinical InformaticsThe Senior Associate, CDS - Clinical Informatics will: - Provide day to day support to a local Operational Strategy & Planning team so as to efficiently and effectively model and forecast from feasibility data and other relevant information to allow for the development of evidence-based planning associated with the implementation and conduct of clinical trials - Coaching and mentoring of relevanthttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1336381Thu, 07 Jul 2016 12:37:20 GMT1336371Sr Associate CDS Clinical InformaticsThe Senior Associate, CDS - Clinical Informatics will: - Provide day to day support to a local Operational Strategy & Planning team so as to efficiently and effectively model and forecast from feasibility data and other relevant information to allow for the development of evidence-based planning associated with the implementation and conduct of clinical trials - Coaching and mentoring of relevanthttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1336371Thu, 07 Jul 2016 12:37:20 GMT1336365Sr Associate CDS Clinical InformaticsThe Senior Associate, CDS - Clinical Informatics will: - Provide day to day support to a local Operational Strategy & Planning team so as to efficiently and effectively model and forecast from feasibility data and other relevant information to allow for the development of evidence-based planning associated with the implementation and conduct of clinical trials - Coaching and mentoring of relevanthttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1336365Thu, 07 Jul 2016 12:37:20 GMT1336359Sr Associate CDS Clinical InformaticsThe Senior Associate, CDS - Clinical Informatics will: - Provide day to day support to a local Operational Strategy & Planning team so as to efficiently and effectively model and forecast from feasibility data and other relevant information to allow for the development of evidence-based planning associated with the implementation and conduct of clinical trials - Coaching and mentoring of relevanthttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1336359Thu, 07 Jul 2016 12:37:20 GMT1336342Sr Associate CDS Clinical InformaticsThe Senior Associate, CDS - Clinical Informatics will: - Provide day to day support to a local Operational Strategy & Planning team so as to efficiently and effectively model and forecast from feasibility data and other relevant information to allow for the development of evidence-based planning associated with the implementation and conduct of clinical trials - Coaching and mentoring of relevanthttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1336342Thu, 07 Jul 2016 12:37:19 GMT1335438Clinical 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=1335438Wed, 06 Jul 2016 05:27:14 GMT1335050Clinical 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=1335050Tue, 05 Jul 2016 15:09:07 GMT1335040Clinical 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=1335040Tue, 05 Jul 2016 15:09:07 GMT1335034Clinical 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=1335034Tue, 05 Jul 2016 15:09:07 GMT1335030Clinical 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=1335030Tue, 05 Jul 2016 15:09:06 GMT1334807Sr CRA Line Manager Home BasedSr. CRA Line Manager Location: Remote/Home-based Covance's Early Clinical Development team is seeking a Sr. CRA Line Manager for a home-based opportunity. Responsibilities include: - Responsible for appropriate management and resolution of performance issues - Measure performance indicators for assigned staff within Clinical Operations - Identify individual training needs and assist in the conduhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334807Fri, 01 Jul 2016 14:51:50 GMT1334801Sr CRA Line Manager Home BasedSr. CRA Line Manager Location: Remote/Home-based Covance's Early Clinical Development team is seeking a Sr. CRA Line Manager for a home-based opportunity. Responsibilities include: - Responsible for appropriate management and resolution of performance issues - Measure performance indicators for assigned staff within Clinical Operations - Identify individual training needs and assist in the conduhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334801Fri, 01 Jul 2016 14:51:47 GMT1334784Sr CRA Line Manager Home BasedSr. CRA Line Manager Location: Remote/Home-based Covance's Early Clinical Development team is seeking a Sr. CRA Line Manager for a home-based opportunity. Responsibilities include: - Responsible for appropriate management and resolution of performance issues - Measure performance indicators for assigned staff within Clinical Operations - Identify individual training needs and assist in the conduhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334784Fri, 01 Jul 2016 14:51:45 GMT1334776Associate Manager Early Clinical Development Home BasedAssociate CRA Line Manager, Early Clinical Development Location: Remote/ Home-based Covance's Early Clinical Development (ECD) team is seeking an Associate CRA Line Manager for a home-based opportunity. In this role you'll work with our Monitoring Excellence Academy new-to-role CRAs and support their training in the CRA position. Managing a team of CRAs at Covance can lead you to a more fulfillihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334776Fri, 01 Jul 2016 14:49:33 GMT1334770Associate Manager Early Clinical Development Home BasedAssociate CRA Line Manager, Early Clinical Development Location: Remote/ Home-based Covance's Early Clinical Development (ECD) team is seeking an Associate CRA Line Manager for a home-based opportunity. In this role you'll work with our Monitoring Excellence Academy new-to-role CRAs and support their training in the CRA position. Managing a team of CRAs at Covance can lead you to a more fulfillihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334770Fri, 01 Jul 2016 14:49:33 GMT1334417Clinical Research Associate I CRA up to 15K Sign on Bonus Seeking Remote Clinical Research Associate I (0-2 years monitoring Experience ) 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 ahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334417Thu, 30 Jun 2016 13:40:30 GMT1334407Clinical Research Associate I CRA up to 15K Sign on Bonus Seeking Remote Clinical Research Associate I (0-2 years monitoring Experience ) 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 ahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334407Thu, 30 Jun 2016 13:40:30 GMT1334401Clinical Research Associate I CRA up to 15K Sign on Bonus Seeking Remote Clinical Research Associate I (0-2 years monitoring Experience ) 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 ahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334401Thu, 30 Jun 2016 13:40:30 GMT1334395Clinical Research Associate I CRA up to 15K Sign on Bonus Seeking Remote Clinical Research Associate I (0-2 years monitoring Experience ) 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 ahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334395Thu, 30 Jun 2016 13:40:30 GMT1334375Clinical Research Associate I CRA up to 15K Sign on Bonus Seeking Remote Clinical Research Associate I (0-2 years monitoring Experience ) 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 ahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334375Thu, 30 Jun 2016 13:40:30 GMT1334338Senior Clinical Research Associate CRA up to 15K Sign on Bonus Seeking Remote Senior Clinical Research Associates (4+ years monitoring Experience ) 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 guidelihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334338Thu, 30 Jun 2016 13:40:29 GMT1334328Senior Clinical Research Associate CRA up to 15K Sign on Bonus Seeking Remote Senior Clinical Research Associates (4+ years monitoring Experience ) 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 guidelihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334328Thu, 30 Jun 2016 13:40:29 GMT1334322Senior Clinical Research Associate CRA up to 15K Sign on Bonus Seeking Remote Senior Clinical Research Associates (4+ years monitoring Experience ) 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 guidelihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334322Thu, 30 Jun 2016 13:40:29 GMT1334316Senior Clinical Research Associate CRA up to 15K Sign on Bonus Seeking Remote Senior Clinical Research Associates (4+ years monitoring Experience ) 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 guidelihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334316Thu, 30 Jun 2016 13:40:29 GMT1334296Senior Clinical Research Associate CRA up to 15K Sign on Bonus Seeking Remote Senior Clinical Research Associates (4+ years monitoring Experience ) 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 guidelihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334296Thu, 30 Jun 2016 13:40:29 GMT1334259Clinical Research Associate II CRA up to 15K Sign on Bonus Seeking Remote Clinical Research Associates II (2-4 years monitoring Experience ) 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 guidelineshttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334259Thu, 30 Jun 2016 13:40:28 GMT1334249Clinical Research Associate II CRA up to 15K Sign on Bonus Seeking Remote Clinical Research Associates II (2-4 years monitoring Experience ) 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 guidelineshttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334249Thu, 30 Jun 2016 13:40:28 GMT1334243Clinical Research Associate II CRA up to 15K Sign on Bonus Seeking Remote Clinical Research Associates II (2-4 years monitoring Experience ) 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 guidelineshttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334243Thu, 30 Jun 2016 13:40:28 GMT1334237Clinical Research Associate II CRA up to 15K Sign on Bonus Seeking Remote Clinical Research Associates II (2-4 years monitoring Experience ) 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 guidelineshttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334237Thu, 30 Jun 2016 13:40:28 GMT1334217Clinical Research Associate II CRA up to 15K Sign on Bonus Seeking Remote Clinical Research Associates II (2-4 years monitoring Experience ) 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 guidelineshttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334217Thu, 30 Jun 2016 13:40:27 GMT1334197Clinical Research Associate CRA Limited Travel 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=1334197Thu, 30 Jun 2016 13:40:23 GMT1334196Clinical Research Associate CRA Limited Travel 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=1334196Thu, 30 Jun 2016 13:40:23 GMT1334183Senior Manager 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=1334183Thu, 30 Jun 2016 13:39:25 GMT1334173Senior Manager 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=1334173Thu, 30 Jun 2016 13:39:25 GMT1334167Senior Manager 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=1334167Thu, 30 Jun 2016 13:39:25 GMT1334161Senior Manager 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=1334161Thu, 30 Jun 2016 13:39:25 GMT1334142Senior Manager 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=1334142Thu, 30 Jun 2016 13:39:25 GMT1333864Sr Manager Central MonitoringCovance needs a Senior Manager, Central Monitoring who: - Prepares and provides RBM proposal text & review of costing, contributes to proposal strategy and development. - Collaborates in the development of RBM sponsor presentations/bid defense support. - Oversees at a study or tactical level tracking data to ensure it is used to effectively to anticipate and mitigate risk. - Leads, plans, preparehttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1333864Wed, 29 Jun 2016 14:52:01 GMT1333854Sr Manager Central MonitoringCovance needs a Senior Manager, Central Monitoring who: - Prepares and provides RBM proposal text & review of costing, contributes to proposal strategy and development. - Collaborates in the development of RBM sponsor presentations/bid defense support. - Oversees at a study or tactical level tracking data to ensure it is used to effectively to anticipate and mitigate risk. - Leads, plans, preparehttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1333854Wed, 29 Jun 2016 14:52:01 GMT1333848Sr Manager Central MonitoringCovance needs a Senior Manager, Central Monitoring who: - Prepares and provides RBM proposal text & review of costing, contributes to proposal strategy and development. - Collaborates in the development of RBM sponsor presentations/bid defense support. - Oversees at a study or tactical level tracking data to ensure it is used to effectively to anticipate and mitigate risk. - Leads, plans, preparehttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1333848Wed, 29 Jun 2016 14:52:01 GMT1333842Sr Manager Central MonitoringCovance needs a Senior Manager, Central Monitoring who: - Prepares and provides RBM proposal text & review of costing, contributes to proposal strategy and development. - Collaborates in the development of RBM sponsor presentations/bid defense support. - Oversees at a study or tactical level tracking data to ensure it is used to effectively to anticipate and mitigate risk. - Leads, plans, preparehttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1333842Wed, 29 Jun 2016 14:52:01 GMT1333823Sr Manager Central MonitoringCovance needs a Senior Manager, Central Monitoring who: - Prepares and provides RBM proposal text & review of costing, contributes to proposal strategy and development. - Collaborates in the development of RBM sponsor presentations/bid defense support. - Oversees at a study or tactical level tracking data to ensure it is used to effectively to anticipate and mitigate risk. - Leads, plans, preparehttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1333823Wed, 29 Jun 2016 14:52:01 GMT1333457Senior Project ManagerCurrent opening for a Clinical Project Manager in our ECD group (Early Clinical Development). Ideal candidate will have Central Nervous and/or Immunology Experience ! As a Clinical Project Manager you will: Lead core project team and facilitate team's ability to lead extended/complete project team. Depending on size and scope of project, this job duty may be performed in collaboration with a Senhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1333457Tue, 28 Jun 2016 12:51:06 GMT1333453Senior Project ManagerCurrent opening for a Clinical Project Manager in our ECD group (Early Clinical Development). Ideal candidate will have Central Nervous and/or Immunology Experience ! As a Clinical Project Manager you will: Lead core project team and facilitate team's ability to lead extended/complete project team. Depending on size and scope of project, this job duty may be performed in collaboration with a Senhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1333453Tue, 28 Jun 2016 12:51:04 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 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 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 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 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