Quotient Sciences
Join our Regulatory Affairs team as an Associate supporting clinical trial approvals and compliance with UK regulations. The role involves document preparation, liaising with regulatory bodies, and maintaining records for early phase clinical trials in Nottingham.
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.
17% below the average for this role
Regulatory Affairs Manager
Cancer Research UK
Regulatory Affairs Start-Up Specialist Senior-CC
University of Pennsylvania
Clinical Research Associate-Regulatory
Eisenhower Health
Regulatory Medical Writer
Cancer Research UK Jersey
Director of Regulatory & Administrative Affairs
mountsinaihospital.com
Regulatory Affairs Specialist-CC
University of Pennsylvania