Clinical Research Coordinator needed in Princeton, NJ

Clinical Research Coordinator needed in Princeton, New Jersey!

 

This is a contract opportunity through MedFocus. We offer:

- Medical and Dental Insurance

- 401 (k)

- LTD

- Excellent hourly compensation

- The opportunity to work with clinical research professionals.

 

RESPONSIBILITIES:

 

Maintain site files, trial master files and study documentation. May distribute study related materials to sites - protocol, IDB etc. Will maintain status reports and document quality control. Review and process regulatory documentation, ensure the execution of clinical trials in a timely, efficient manner, working within established timelines and budgets. Track clinical trial supplies, patient recruitment activities, and Serious Adverse Events, and may conduct query resolution. Identify investigator sites for participation in trials, through feasibility and organize investigator meetings. Collect and maintain a file of regulatory documents, study documentation and communication for each study. Consistently track and update study metrics in internal systems and report such to PM. May be responsible for ancillary and drug supply management with or without IVRS.

 

QUALIFICATIONS:

 

Qualified candidates must have 1-2 years experience working with clinical research studies. Must have previous clinical trial support experience. A Bachelors degree or registered nurse required. Must have excellent written and oral communication skills.