Job Description
📋 Description Serve as site manager; ensure data entry, query resolution, audit readiness. Monitor study activities: site management, initiation, monitoring, closeout. Monitor compliance with study protocols and regulatory guidelines. Prepare study conduct requirements and train sites. Manage device accountability, inventory, and distribution; track issues. Draft regulatory documents; CRFs, protocols, manuals; mentor staff. 🎯 Requirements Bachelor’s degree in Biological sciences/health field; 5+ yrs clinical research; 2+ yrs monitoring. Strong knowledge of medical terminology. Knowledge of laws/regulations governing clinical studies. Excellent verbal, written, and interpersonal communication. 40-60% travel; strong organizational and problem-solving skills. MS Office proficiency; ability to mentor junior staff. 🎁 Benefits Collaborative team with constant learning. Part of a team advancing treatments for serious diseases. Generous benefits: medical, dental, vision, life, AD&D, disability. 401(k) with employer match; paid parental leave. Eleven company holidays and at least 15 vacation days. Paid sick time per applicable law.
