Sr. Clinical Research Associate

Exact Sciences

Base: $91,000.00 - $155,000.00 (national); bonus e...
Fully remote
4+ years clinical research monitoring experience
Bachelor's degree or equivalent experience
Gcp/ich protocol compliance knowledge
Exact Sciences is seeking a Senior Clinical Research Associate (CRA) to manage and conduct projects related to clinical study plans, ensuring compliance and effective communication between clinical sites and the project team. The position is fully remote, emphasizing a purpose-driven culture and a commitment to cancer prevention and detection

Job Summary

  • The role involves executing and managing projects associated with company clinical study plans while acting as a lead CRA to support the team.
  • Candidates will conduct comprehensive site qualification, initiation, and routine monitoring visits to ensure GCP/ICH/Protocol compliance and accurate data collection.
  • Exact Sciences offers robust benefits including paid time off, health coverage, and a retirement savings plan alongside a purpose-driven career in cancer prevention.

Matching Summary

Match Score: 85

Exact Sciences is seeking a Senior Clinical Research Associate (CRA) to manage and conduct projects related to clinical study plans, ensuring compliance and effective communication between clinical sites and the project team. The position is fully remote, emphasizing a purpose-driven culture and a commitment to cancer prevention and detection.

Salary

Base: $91,000.00 - $155,000.00 (National); Bonus eligible; Benefits: Medical, dental, vision, PTO, retirement plan

Skills & Requirements

Must-have

  • 4+ years clinical research monitoring experience
  • Bachelor's degree or equivalent experience
  • GCP/ICH protocol compliance knowledge
  • Site initiation and close-out visit execution
  • Source data verification and query resolution
  • Electronic Data Capture (EDC) system proficiency

Nice-to-have

  • Experience with In Vitro Diagnostics (IVD)
  • FDA submission process knowledge (IDE, PMA, 510k)
  • Mentoring junior CRAs or staff
  • eTMF systems and document management
  • Inclusion mindset and teamwork values

Key Requirements

  • Bachelor's degree or 6+ years monitoring experience
  • Minimum 4 years clinical research monitoring experience
  • Authorization to work in the United States without sponsorship

Work Rights

Must have US work authorization without sponsorship

Tailored Resume

Cover Letter