Clinical Research Quality Manager Jobs

Communicates with Sponsored Programs Administration to ensure proper management of charges and billing.

Recruits, interviews and obtains informed consent from prospective subjects for entrance into clinical trials and studies.

Coordinators appropriate laboratory tests and other procedures for subjects participating in studies; including drawing blood or collection of other samples.

Coordinates with Investigational Pharmacy for subjects to receive required drugs.

Coordinates and submits IRB protocols, reports, revisions, updates, approvals.

Records appropriate clinical and laboratory data on forms provided by the principal investigator(s), federal government, and/or industry sponsors.

Clinical research in Oncology experience: 2 years, required

Minimum of 5+ years of previous Quality Assurance experience in clinical research, required.

Patient First – Keeping the patient at the center of everything we do

Accountability – Taking responsibility for our actions

Commitment & Care – Upholding FCS vision through every action

Team – Working together, one team, one mission