Senior Clinical Research Associate
Core
Monitoring and owning the progress of clinical studies at investigative sites to ensure compliance with protocol, SOPs, and regulations.
Role type
Senior Clinical Research Associate (IC)
Builds
Clinical trials across various therapeutic areas
Domain
Clinical Research / CRO / Pharmaceutical
Required skills
Clinical trial monitoring, Regulatory compliance (ICH-GCP), Site management, Risk identification and mitigation, Conflict resolution, Financial management (for Senior level), Study startup coordination
Preferred skills
Graduate or postgraduate degree in scientific/healthcare discipline, Experience in study startup activities
Technologies
Clinical trial management systems, Regulatory submission tools
Responsibilities
Monitor and own the progress of clinical studies at investigative sites, Coordinate study setup activities (identify investigators, prepare regulatory submissions, conduct pre-study and initiation visits), Interact directly with clients and participate in proposal activities, Train and mentor junior staff members (via careerplan.io/jobs/6202570004-senior-clinical-research-associate-at-precisionmedicinegroup)
Seniority
Senior, hands-on IC with mentorship responsibilities