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Responsibilities:
- Oversee all site monitoring activities including routine monitoring, close-out, and file maintenance.
- Ensure study staff have proper materials and instructions, and verify informed consent and protocol adherence.
- Monitor data integrity via source document review and CRF verification.
Qualifications:
- University degree or certification in a related allied health profession (e.g., nursing licensure).
- 4+ years of clinical monitoring experience.
- 50-60% overnight travel required.
Work Environment:
- Fast-paced, technology-based environment with changing priorities.
- Frequent travel to client/site locations, both domestic and international.
- Ability to sit for extended periods, operate a vehicle, and lift up to 20 lbs.
Fortrea
Fortrea is a clinical research organization that helps biopharmaceutical and medical device companies bring life-saving therapies to patients. The company emphasizes a collaborative, family-oriented culture with a focus on teamwork and excellence, employing a large workforce globally.