This clinician will provide medical oversight for clinical research studies, serving as Medical Monitor and supporting participant safety, protocol execution, and scientific review. The work centers on global and pan-regional trials, with collaboration across cross-functional study teams, sponsors, and Medical & Safety colleagues. This is a remote role with responsibilities that include protocol development, safety review, and client-facing scientific support.
Key Responsibilities
- Provide medical oversight for assigned clinical research studies as the Medical Monitor.
- Lead global and pan-regional trials as a Global Lead Medical Monitor.
- Review serious adverse events and support medical management with Medical & Safety teams.
- Deliver protocol-specific and therapeutic area training to project teams.
- Contribute clinical and scientific input to protocols, development programs, publications, and other medical deliverables.
- Support feasibility assessments, proposal development, and client meetings.
- Review clinical study reports and other key study documentation.
- Partner with cross-functional teams to support project delivery, compliance, and client satisfaction.
Required
- Medical degree from an accredited institution.
- At least 2 years of medical monitoring experience in clinical research or a related industry.
- Strong knowledge of GCP, clinical development, safety processes, and applicable regulatory requirements.
- Experience reviewing safety data and supporting serious adverse event assessment and management.
- Proficiency in English.
- Valid passport and ability to travel as required.
Preferred
- Experience supporting neurology-related clinical research.
- Experience mentoring medical colleagues.
- Experience in sponsor engagement or business development support.
Benefits & Perks
- Remote work with collaboration across global teams and multiple time zones.
- Competitive benefits package, depending on location.
- Transparent salary range disclosed for the role.
- Opportunity to work on global clinical trials and clinical development programs.