Senior Research Physician/Medical Monitor
$100 - $115 per hourMedasource
Senior Research Physician (SRP) / Medical Monitor
Location : Horsham, PA (Hybrid – 3 days onsite/week )
Contract Length : 6-month contract with strong likelihood of extension
Schedule : Full-time | 40 hours/week
Start Date : ASAP
Pay Rate : $100–$115/hr
Overview
We are seeking an experience d Senior Research Physician (SRP) / Medical Monitor to support a high-profile clinical trial within the Autoantibody Therapeutic Area of a leading pharmaceutical organization. This individual will provide senior-level medical oversight, clinical leadership, and operational support for a complex clinical study.This role is critical in maintaining study momentum, ensuring participant safety, and partnering cross-functionally with clinical operations, regulatory affairs, biostatistics, and data management teams.
Key Responsibilities:
- Serve as the primary Medical Monitor and provide clinical oversight for study-related medical decisions
- Review and assess AEs, SAEs, protocol deviations, and emerging safety signals
- Provide hands-on clinical operations oversight to support study timelines, milestones, and quality standards
- Partner with Clinical Operations teams to identify and resolve study execution challenges
- Support protocol execution, data review activities, and study-level decision making
- Collaborate cross-functionally with Regulatory Affairs, Biostatistics, Data Management, and other key stakeholders
Must-Have Qualifications:
- Medical degree ( MD or equivalent required )
- Experience as a Senior Research Physician, Clinical Research Physician, or Medical Monitor within pharmaceutical/biotech clinical development
- Strong clinical operations oversight experience
- Experience supporting clinical trial execution, safety monitoring, AE/SAE review, and protocol compliance
- Ability to provide medical leadership in a fast-paced clinical development environment
- Strong cross-functional communication skills
Nice-to-Have Experience:
- Board certification or advanced training in Rheumatology, Immunology, or a related specialty
- Experience within autoimmune, rheumatology, or autoantibody therapeutic areas
- Experience supporting complex clinical trial designs
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