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Clinical Data Manager Jobs

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Description: The objective of a Clinical Data Manager II (CDM II) is to act as a lead data manager for one or more projects. CDM II's lead multiple, high volume/highly complex studies. He/she independently leads and/or efficiently performs, with quality, all data management activities within an assigned study. CDM II's may mentor junior level staff on all associated tasks within a study. Liaise ...

Description: The objective of a Clinical Data Manager II (CDM II) in our Phase I department is to act as a lead data manager for one or more projects. CDM II's lead multiple, high volume/highly complex studies. He/she independently leads and/or efficiently performs, with quality, all data management activities within an assigned study. CDM II's may mentor junior level staff on all associated tas...

Ascent Pharma is seeking a Clinical Data Associate II and a Clinical Data Manager!!! ***APPLY TODAY OR REFER A FRIEND! We offer a terrific referral bonus! Divna Rosenzweig/Sr. Clinical Development Recruiter (310) 933-4549 Please send resumes directly to ***** Clinical Data Associate II Specific Responsibilities: This role will immediately assume study lead data management ...

The Principal Clinical Data Manager, Clinical Data Management, is responsible for leading study data management activities including, but not limited to, coordination of CRF design, development, review and sign off ; Reviews and approves CRO generated Data Management documents, coordinates database live and close out activities with the CRO, provides guidance to CRO to manage query flow and implem...

Ascent Pharma is seeking a Clinical Data Associate II and a Clinical Data Manager!!! ***APPLY TODAY OR REFER A FRIEND! We offer a terrific referral bonus! Divna Rosenzweig/Sr. Clinical Development Recruiter (310) 933-4549 Please send resumes directly to ***** Clinical Data Associate II Specific Responsibilities:This role will immediately assume study lead data management r...

Primary point of contact providing guidance and oversight of Clinical Data Management activities supporting study start up, in stream production data review, and database closure across Client Projects. Manage budgets, timelines, and resources while ensuring compliance with GCP regulations, policy and Client Company policy. • Manage all operational aspects of clinical trials in compliance with GC...

Primary point of contact providing guidance and oversight of Clinical Data Management activities supporting study start up, in stream production data review, and database closure across Client Projects. Manage budgets, timelines, and resources while ensuring compliance with GCP regulations, policy and Client Company policy. • Manage all operational aspects of clinical trials in compliance with GC...

Primary point of contact providing guidance and oversight of Clinical Data Management activities supporting study start up, in stream production data review, and database closure across Client Projects. Manage budgets, timelines, and resources while ensuring compliance with GCP regulations, policy and Client Company policy. • Manage all operational aspects of clinical trials in compliance with GC...

Primary point of contact providing guidance and oversight of Clinical Data Management activities supporting study start up, in stream production data review, and database closure across Client Projects. Manage budgets, timelines, and resources while ensuring compliance with GCP regulations, policy and Client Company policy. •Manage all operational aspects of clinical trials in compliance with GCP...

Primary point of contact providing guidance and oversight of Clinical Data Management activities supporting study start up, in stream production data review, and database closure across Client Projects. Manage budgets, timelines, and resources while ensuring compliance with GCP regulations, policy and Client Company policy. •Manage all operational aspects of clinical trials in compliance with GCP...

Primary point of contact providing guidance and oversight of Clinical Data Management activities supporting study start up, in stream production data review, and database closure across Client Projects. Manage budgets, timelines, and resources while ensuring compliance with GCP regulations, policy and Client Company policy. •Manage all operational aspects of clinical trials in compliance with GCP...

TechData is looking for HEOR (Outcome Research Biostatistician),Biostatistician/SAS Programmer/Statistical Programmer (Some can be telecommuting), Clinical Programmer (Oracle clinical, Rave, Inform), Clinical Data Manager, Clinical Research Scientist/Associate, Sr. Study Manager, Drug Safety Associate inNorthern and Central NJ.Please see below requirements and send your resume to: John.zhang@techd...

Just thought I would post a quick update as I am still looking for roughly 3-4 Clinical Data Managers to assist. For the next 12+ months, with a massively increased pipeline, for a Global CRO that I work very closely with. Now this role is definitely aimed towards candidates who are interested in expanding their skill set, as well as gain solid professional experience. While it is also a great pos...

Immediate Need In the Northern California Bay Area for a: Senior Clinical Data Manager and a Senior SAS Clinical Programmer Solid Pharma Sponsor Start-up in need of two sharp individuals for their growing team. Excellent salaries, benefits and lots of opportunity for growth. 1. Clinical Data Manager: We need someone with heavy "hands-on" clinical CDM experience who can also manage outside CRO...

Position TitleCLINICAL DATA SPEC III, DCRI Clinical Events & SafetyRequisition Number400936783Auto req ID66935BRLocationDurhamDuke EntityMEDICAL CENTERDepartment NameDCRI - Clinical Events CommiteeShiftFirst/DayFull Time / Part TimeFULL TIMEJob Code2355 CLINICAL DATA SPEC III, DCRIJob Family Level72Job Description **Strong preference for candidates with at least three years of direct People Manag...

This position functions independently and in a supervisory role for all team members that are assigned. This position is responsible for managing data quality, data review, and data backup. Additional responsibilities include managing monitor visits and upcoming audits/data locks in accordance with Good Clinical Practice Guidelines, federal and sponsor regulations and guidelines, Vanderbilt Policy...

Description This position functions independently and in a supervisory role for all team members that are assigned. This position is responsible for managing data quality, data review, and data backup. Additional responsibilities include managing monitor visits and upcoming audits/data locks in accordance with Good Clinical Practice Guidelines, federal and sponsor regulations and guidelines, Vand...

**Strong preference for candidates with at least three years of direct People Management/Supervision and Project Management skills. OCCUPATIONAL SUMMARY The Clinical Event CDS III independently plans, conducts and reports the data management portion of large, complex or international projects and provides leadership on the value and best practices for clinical event adjudication (CEC), safety su...

Attention current TriHealth employees: Please apply for this position by submitting an online internal application via SuccessFactors. Please be certain to update your SuccessFactors Employee Profile prior to applying to this position. CLINICAL DATA ANALYST-CLINICAL QUALITY: Under the supervision of the manager/supervisor of the Clinical Quality Resources Department this position is responsible ...

CLINICAL DATA ANALYST-CLINICAL QUALITY TriHealth Good Samaritan Hospital in Cincinnati, Ohio FT, days (#72226) Under the supervision of the manager/supervisor of the Clinical Quality Resources Department this position is responsible for design and implementation of data integrity programs and the development and publication of standard and ad hoc reports for end-users. This includes responsibil...