Clinical Research Manager

As the Clinical Research Coordinator at Clemente Clinical Research, you will work with a team that is dedicated to bringing quality care to those in the community that need it most.

As a member of our team, you will::

• Work with our physicians across multiple clinics to recruit, screen, and enroll patients that meet the trails’ protocol inclusion and exclusion criteria

• Review and comprehend all study protocols

• Coordinates and attends monitor site visits and prepares site visit documentation

• Ensure study staff is properly trained on trial protocols

• Manage patient scheduling and follow-up activities

• Facilitate and coordinate the daily clinical trial activities and play a critical role in the conduct of

the study

• Create, manage, and maintain documentation for each trail

• Collect protocol data and enters information into the electronic data capture (EDC) system

• Act as a secondary reviewer to ensure the trail protocols are being conducted accurately

• Works with the monitor to ensure protocol guidelines and deadlines are being met

• Works with sponsor and IRB to collect updated medical history, adverse events, serious adverse

events

• Order study supplies and keep track of inventory levels

Experience:

5+ years as a Clinical Research Coordinator (CRC)

Fluent in English and Spanish

Phlebotomy certificate

Experience and training in the conduct of clinical research (specific experience and/or training in clinical research, including IRB submissions, reporting and source documentation, trial management).

A thorough understanding of regulatory requirements, principles of GCP and biomedical research ethics.