ThinkCentric's Clinical Research Staffing group assists leading Pharmaceutical and Biotechnology companies fulfill their growing needs for the execution of timely and cost effective clinical trials.  We have specialized recruiting capabilities to qualify candidates in clinical trial management expertise and concomitant trial services.

Our clinical recruiting team has staffed entry level through Senior Director positions in world class pharmaceutical companies on a permanent or contract basis in:

• Clinical Operations
• Clinical Science
• Drug Safety
• Data Management
• Medical and Regulatory Affairs
• Contract and Outsource Management

We are highly competent in qualifying In-house and Regional CRAs vis-a-vis scope and depth of trial experience.  We determine abilities from study start-up through database lock including Investigator selection, Investigator Meeting participation, Site Monitoring, SAE reporting, and use of IVRS, EDC, and Clinical databases for the Phases and Therapeutic Areas worked.

We are able to evaluate Clinical Trial Managers' depth of expertise in CRF and Protocol development, study, and project management.

We also evaluate medical writing skills for both Clinical Study and Regulatory reporting.