Quotient Sciences
This role oversees all screening activities, personnel, and volunteer recruitment while ensuring strict adherence to Good Clinical Practice (GCP) guidelines. The incumbent manages clinical teams, monitors subject safety and data quality, and coordinates recruitment processes to optimize operational efficiency. Responsibilities include reviewing protocols, obtaining informed consents, evaluating medical histories, and reporting compliance issues to maintain high study standards.
Headquarters
Nottingham, England, United Kingdom
Company Size
1001-5000 employees
Founded
1990
Quotient Sciences is a global contract research, development and manufacturing organization (CRDMO) that accelerates drug development from candidate selection through commercial launch. They provide integrated services for small molecule drugs and novel therapies, including Phase 1 clinical trials, formulation development, and drug manufacturing. Science-led insight and an end-to-end platform enable faster translation of molecules to patients, supporting sponsors with clinical research, development, and commercial-scale supply.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Quotient Sciences.
Quotient Sciences didn’t post a salary, so this is our estimate from similar listings.
18% below the average for this role
Human Subject Research Coordinator
University of Rochester
Research Associate III
montefioremedicalcenter.com
Clinical Research Coordinator
OhioHealth
CRA I, Australia (no monitoring experience required)
Syneos Health
Clinical Research Coordinator I
UMass Chan Medical School
Clinical Research Coordinator
OhioHealth