Clinical Research Coordinator (CRC)


IQVAMED understand your project’s values
The CRC has multiple responsibilities to manage the clinical research/trials at the sites and interact with sponsor personnel to resolved the queries.

What are the most important and challengeable factors in a CRO/sponsor’s determination of which sites to pick for a study?

Many Sponsors won’t even consider using an investigator or sites who does not have a CRC.

As your IQVAMED provides (CRCs) Services to the CROs/Sponsors (Pharmaceutical, Biotechnology, and Medical devices companies) and in a wide range of therapeutic areas, we also provide complete clinical trial supports with our experienced or competent Clinical Research Coordinators (CRCs). The CRC is the primary person who interacts with the Institutional Ethics Committee at most investigative sites and plays vital role for study conduct. Our skilled coordinators are well prepared for the site visit and ready to show their site at its best.

Why Our CRCs Services?

A survey demonstrated that the number of CRCs who have been in their current position for 2 or less than 2 years. And It is also true that many CRCs are taking new jobs as clinical research associates CRAs) or other designations for Sponsors or CROs. In this case trials are deviated from continues track of execution. IQVAMED screened & recruits only those candidates who love the position of clinical research and committed or willing to complete the assigned sponsor studies

Our CRCs Have