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Clinical Research Coordinator (OCRP)

Clinical Research Coordinator
Ohio Clinical Research Partners, LLC

Qualified candidate will assist the research team in the implementation and conduction of clinical trials per federal, state and institutional guidelines by performing tasks delegated by research team members including investigators, managers and coordinators. Responsibilities during all phases of trials from pre-study implementation through study closure are included in the scope of this position.

If you are looking for a company that encourages its employees to excel and provides a welcoming environment, then we have a wonderful opportunity for you! We are looking for an experienced Clinical Research Coordinator to join our team. This position will be fulltime.

Please note, this position will work out of our Eastside & Westside client offices.

Job Functions
Assists with the implementation and conduct of clinical research projects as delegated to assure successful achievement of quality, safety, regulatory, and financial outcomes.
Performs specific technical tasks/procedures and records data as assigned.
Assists with approved research subject recruitment, retention, and communications.
Maintains inventory of study-specific supplies and standard department-specific clinical supplies and work areas to assure protocol compliance and efficient workflow.

Requirements
RN, LPN, Experienced Medical Assistants
Phlebotomy skills required
Knowledge of all aspects of Phase II-IV clinical trials. Willing to train a qualified candidate.
Organizational skills a must for the position
Experience using MS Word and Excel
Travel required between various sites

How to Apply
We offer a complete compensation package including health and ancillary benefits, 401(k) plan with company match, and generous paid time off. For consideration, please apply using this job site. When applying, please include "OCRP RESUME" in the subject line of your email.

We are an equal opportunity employer

Unsolicited resumes from third party agencies or recruiting firms should not be submitted.

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