Assistant Director of Drug Development

Florida Cancer Specialists & Research Institute Clinical Expertise And Real-World Evidence Capabilities Advancing Treatment of Blood Cancers

Veeva MedTech adoption boosts clinical trials

Sector Update: Health Care Stocks Mixed Late Afternoon

Veeva and Sarah Cannon Research Institute Form Strategic Collaboration to Advance Oncology Clinical Trials

Clinical Document Control Quality Manager

Sarah Cannon Research Institute (SCRI) is a leading oncology research organization focused on advancing cancer therapies through community-based clinical trials. The Clinical Document Control Quality Manager is responsible for the creation, management, and improvement of clinical research documents and procedures, ensuring compliance with industry regulations and supporting process improvements across the organization.

Sr. Manager, Head of Talent Acquisition

Recruiter

Director Safety & Pharmacovigilance 

Clinical Drug Safety Lead

Principal Safety Lead, Regulatory & Pharmacovigilance

Sign up with Google

Sign in with Google