Associate Study Manager

Location: Hybrid in Fairfield County, CT

Drive breakthrough cancer research that changes lives.

My client—one of the most impactful forces in oncology innovation—is expanding its clinical research operations. If you thrive in complex studies, love orchestrating cross-functional execution, and want your work to accelerate cures, this role puts you at the heart of scientific progress.

Why You Should Apply

• Work on high-visibility translational studies within a nationally recognized consortium
• Hybrid flexibility + collaborative, mission-driven culture
• Competitive compensation + strong benefits
• Opportunity to own studies end-to-end in a fast-moving, high-impact organization
• Direct contribution to advancing therapies that have already transformed patient survival
  
  

What You’ll Be Doing

• Lead operational planning, execution, timelines, vendors, and budget oversight
• Drive protocol development, feasibility, site selection, and study documentation
• Manage IRB submissions, regulatory packages, and audit-ready study files
• Oversee CROs, vendors, pharma partners, study metrics, and site communications
• Present study progress to leadership and support risk mitigation strategies
• Maintain eCRFs and database quality (Medidata Rave experience required)
  
  

About You

• 5+ years clinical study operations (oncology strongly preferred)
• Skilled in protocol development, site/vendor oversight, and GCP/ICH compliance
• Strong communicator and study-management problem solver
• Thrives in a fast-paced, collaborative, mission-centric environment
  
  

How To Apply

Email ava@scientificsearch.com with Job #19679 in the subject line.