CLINICAL RESEARCH COORDINATOR

IQVAMED

Services

Clinical Research Coordinator (CRC)

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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

Effective interpersonal skills.
Good communication skills with the ability to communicate effectively with medical personnel.
Passionate towards allocated responsibilities and hardworking.
Effective organizational and time management skills.
Ability to work in a team or independently as required.
Ability to remain flexible and adaptable in a wide range of scenarios.
Excellent understanding and demonstrated application of GCPs and applicable SOPs.
Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents.
Demonstrated understanding of clinical research/therapeutic area knowledge and medical terminology.
Well-developed critical thinking skills, including but not limited to: critical mind set, in-depth investigation for appropriate root cause analysis and problem solving.
Ability to utilize problem-solving techniques applicable to constantly changing environment.

Services

Study Start up and feasibility support.
Submission of trials documents to IRB/IEC support.
Informed Consent process support.
Recruiting subjects
Scheduling subject and sponsor visit.
Audit/ Regulatory Inspection support.
Case Report Form completion supports.

IQVAMED

services

Clinical Research Services

Pharmacovigilance Services

Patient & Healthcare Services

Services

Clinical Research Coordinator (CRC)

Why Our CRCs Services?

Our CRCs Have

Services

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IQVAMED