Position overview
United Research Group is seeking a Clinical Medical Monitor to provide medical and scientific oversight for clinical research studies. This professional will collaborate with investigators, clinical operations teams, and study partners to support participant safety, protocol compliance, and high-quality clinical trial execution.
Responsibilities
- Provide medical oversight and clinical guidance throughout study conduct.
- Review clinical safety information, adverse events, serious adverse events, and emerging safety trends.
- Support medical review of clinical data, laboratory findings, and protocol-defined safety parameters.
- Address medical questions from investigators and clinical operations personnel.
- Assist with protocol development, medical monitoring plans, and clinical risk assessments.
- Participate in safety review meetings and support appropriate escalation of medical concerns.
- Collaborate with clinical data management and pharmacovigilance teams to resolve medical queries.
- Support regulatory inspection readiness and medical documentation.
The qualifications below are proposed recruitment criteria pending final URG approval.
Proposed qualifications
- MD, DO, or equivalent recognized medical degree.
- Active medical licensure where required for assigned responsibilities.
- Clinical research or medical monitoring experience preferred.
- Knowledge of ICH-GCP, clinical trial safety reporting, and applicable regulatory requirements.
- Strong medical judgment, documentation, and communication skills.
- Ability to collaborate with multidisciplinary teams in a remote environment.