Medical Monitor Safety Administrator
Core
Coordinates safety support, protocol inquiries, adverse events, and Data Safety Monitoring Board (DSMB) logistics for global clinical trials.
Role type
Senior project coordination and safety administration specialist
Builds
Clinical trial safety programs and DSMB/EAC operational support
Domain
Clinical research / Pharmaceutical safety
Deliverable
dashboards & analysis
Required skills
Adverse event management, DSMB coordination, contractual document preparation, data privacy compliance, budget management, meeting facilitation, regulatory knowledge (FDA/ICH), data entry and system reconciliation
Preferred skills
Training junior staff, site liaison management, translation coordination
Technologies
MS Office (Word, Excel, PowerPoint, Access), internal/external databases, tracking systems
Responsibilities
Coordinate review of protocol inquiries and adverse events; represent DSMB/EAC teams at meetings; prepare and review contractual documents; compile adjudication dossiers; manage project budgets and expenses; ensure audit-ready program files and data privacy compliance.
Seniority
Mid-level, hands-on IC
