Live opening · Posted 12 days ago
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About the job
Director / Senior Director – Clinical Development, Rheumatology
Remote | United States or Canada | Full-Time | Up to ~25% Travel
Summary
A hands-on Medical Monitoring opportunity within a leading global life sciences organisation supporting late-phase Rheumatology and Immunology clinical programs.
This hire will provide medical leadership across active studies, with responsibility for subject safety, medical oversight, clinical data review, investigator support, and study delivery.
The position offers the opportunity to work closely with sponsors, investigators and cross-functional teams across important autoimmune indications including Lupus, Rheumatoid Arthritis, Systemic Sclerosis / Scleroderma and Sjögren’s Syndrome.
Ideal background:
MD/DO with formal Rheumatology training
Board certification preferred; internationally trained Rheumatologists can also be considered
Strong understanding of Rheumatology clinical research and industry-sponsored drug development
Ideally 2+ years of hands-on Medical Monitoring / Clinical Development experience within pharma, biotech or CRO
Alternatively, experienced Rheumatology PIs / Clinical Investigators with substantial pharmaceutical-sponsored Phase II/III trial experience can be considered
Strong exposure to autoimmune indications, ideally including: SLE / Lupus Nephritis, Sjögren’s Syndrome, Systemic Sclerosis / Scleroderma, Rheumatoid Arthritis
Experience with Phase II / III clinical trials
Comfortable operating in a hands-on, delivery-focused Medical Monitoring environment
What You’ll Do
Serve as Medical Monitor for assigned Rheumatology / Immunology clinical studies
Provide medical oversight relating to subject eligibility, safety, protocol interpretation and study conduct
Review clinical and safety data, including AEs/SAEs, laboratory abnormalities, protocol deviations and emerging safety trends
Act as a medical point of contact for sponsors, investigators, sites and internal study teams
Provide medical input into protocols, amendments, Medical Monitoring Plans and study materials
Support study start-up, feasibility, investigator engagement and ongoing trial execution
Compensation
Base salary: Up to $315,000 USD
Bonus: 30%
Full benefits package
Final level and compensation to be determined based on experience, scope, and overall fit
Work arrangement
No
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