Clinical Research Coordinator

Summary

Experienced candidates with medical backgrounds and excellent interpersonal skills for
the position of Clinical Research Coordinator (CRC). This role is responsible for the successful conduct
of clinical trials under the oversight of the principal investigator. The CRC will be responsible for both
clinical and administrative duties related to the conduct of clinical research at the site.

Responsibilities

Abide by local, state, GCP, ICH and FDA guidelines and regulations for the conduct of clinical trials.

Oversee the smooth running of clinical trials at site in collaboration with study investigator(s) and other team members.

Complete all required organization and study specific training in timely manner, including attendance at offsite investigator meetings.

Supervision and training of site research site staff, including research assistants and lab technicians.

Participate in the planning and conduct of research participant recruitment efforts.

Conduct the proper consent of research participants.

Collecting source obtained from research and transcribe into case report forms.

Perform medically qualified clinical procedures such as vital signs, EKG, and preferably phlebotomy.

Process study labs per requirements.

Collaborate with sponsor/CRO study teams, including prompt resolution of queries and other action items.

Monitoring research participants to ensure adherence to study participation and maintain compliance.

Perform regular inventory checks and ensure the necessary supplies and equipment for a study are in stock and in working order.