Medical Monitor
Core
Provide day-to-day medical oversight for clinical trials to ensure patient safety, data integrity, and protocol compliance.
Role type
Medical Monitor (Clinical Development)
Builds
Clinical trials for medical technology and digital health solutions
Domain
Healthcare / Clinical Trials
Deliverable
client delivery
Required skills
Medical judgment, safety signal evaluation, eligibility assessment, dose modification, risk mitigation, GCP knowledge, AE/SAE review
Preferred skills
Clinical trial methodology, cross-functional collaboration, regulatory documentation
Technologies
None stated
Responsibilities
Provide medical oversight for assigned clinical trials; Review and assess adverse events (AEs) and serious adverse events (SAEs); Serve as key medical contact for investigators; Collaborate with Clinical Operations, Pharmacovigilance, and Data Management; Contribute to clinical study reports and regulatory submission documents
Seniority
Mid-level (3–7 years experience)