Medical Director, Global Rheumatology Lead
job summary:
Medical Director - Rheumatology (Global Indication Lead)
Remote | Must be US based (EST or CST time zones)
Contract, w2 only | 12 Months
Travel | 10 - 20%
We are seeking an experienced Medical Director (Rheumatologist) to serve as Global Indication Lead on behalf of a leading sponsor through a full-time FSP engagement. This fully remote position offers a unique opportunity to drive strategy for a high-priority immunology program, owning the Clinical Development Plan, guiding global study teams, and contributing to the long-range vision of the indication. The ideal candidate will bring specialty training in rheumatology and prior clinical development experience across Phases I-III.
location: Telecommute
job type: Contract
salary: $160 - 180 per hour
work hours: 9 to 5
education: Doctorate
- responsibilities:
- Serve as Global Medical Indication Lead, translating the Target Product Profile into an actionable Clinical Development Plan
- Provide strategic medical leadership across global clinical trials (Phase I through registration) for the assigned indication
- Oversee and mentor Clinical Trial Physicians supporting the program
- Ensure medical consistency and alignment across protocols, documents, and communications
- Lead or contribute to medical advisory boards, internal governance meetings, and regulatory interactions as needed
- Collaborate cross-functionally with Regulatory, Clinical Operations, Biostats, and Medical Writing to ensure timely, high-quality deliverables
- Maintain oversight of trial design, data review, and interpretation, ensuring medical integrity and alignment with program objectives
- Ensure compliance with ICH-GCP and sponsor-specific policies and procedures
- qualifications:
- Medical Degree (MD) required
- Specialty training (e.g., residency or fellowship) in Rheumatology required; relevant clinical and/or research experience and board certification preferred
- Minimum of 5 years of clinical development experience (end to end from Phase 1 to registration) within the pharmaceutical, biotech, or CRO industry
- Demonstrated expertise in clinical trial design, conduct, and data interpretation
- Ability to lead in a global, matrixed environment and provide strategic guidance to clinical teams
- Excellent written and verbal communication skills in English
- Willing to travel up to 10-20% (domestic & international)
- LI-AT1
skills: GCP (Good Clinical Practice), Clinical Study Design, Medical Leadership, Medical Plan Development, ICH Regulations
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [email protected].
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
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