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PharmaNet-Princeton, NJ, 08540
Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators Negotiate study budgets with investigators Obtain, review, and process regulatory and administrative documents from investigator sites Review and develop protocols Review and develop CRFs Coordinate and present at Investigators' Meetings Participate in proposal meeting...
Clinical Research Associate Jobs in Princeton, New Jersey Jobs
Theradex | Princeton, NJ, 08540 |
An opportunity is available for CRA’s based in Princeton. Theradex is looking for motivated individuals with science and research backgrounds who would like the opportunity to become clinical research associates and be involved in the development of many new products being evaluated for the treatment of cancer. Position responsibilities include but are not limited to: - 75% Travel. - Monitoring investigational drug studies in Phases I, II, III, IIIB, and IV, including: a. Source document verification and comparison to CRF data. b. CRF review/retrieval and data corrections. c. Drug accountab...
ClinForce | Princeton, NJ, 08540 | 5
ClinForce is currently seeking a Senior In-House Clinical Research Associate - CRA for Princeton, NJ. Successful candidate will be responsible for performing routine In-House CRA responsibilities and managing the current trial. Candidate will also be assisting the doctor. Position will be 20-30 hours per week for now but could eventually drop to 20 hours per week.. Job Requirements: 5 years of experience within the clinical research industry
PharmaNet Jobs
PharmaNet | Chicago, IL, 60601 | >1
Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators for participation in clinical trials Negotiate study budgets with investigators Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites Develop Case Report Forms for clinical trials Present (e.g. study specific guidelines and procedures, case report forms, and monitoring conventions) at Investigators’ Meetings Prepare and process Serious Advers...
PharmaNet | Boston, MA, 02108 | >3
Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators Negotiate study budgets with investigators Obtain, review, and process regulatory and administrative documents from investigator sites Review and develop protocols Review and develop CRFs Coordinate and present at Investigators' Meetings Participate in proposal meeting...
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