Sr. Medical Director, Rheumatology US Remote

Senior Medical Director Rheumatology - US Remote Based

Raising CRO standards for innovation and delivery to help bring life-changing treatments to patients faster. Fortrea is seeking a dedicatedUS remotebasedMedical Directoror Senior Medical Directorwith deep expertise inRheumatologyalongwith background in innovative therapiesincludingcelland gene therapy.The incumbent will provide medical leadership and oversight across all phases of development including early-phase innovation and late-phase global programs. Responsible for supporting the development activities of proposed and ongoing projects in their area of expertise as well as medical monitoring to assigned clinical studies.

The (Senior) Medical Director will serve as a key medical representative in client interactions businessdevelopment discussions and proposal presentations. The role will further foster and enhance relationships with global clinical operations teams and provide leadership as the Leading Physician for Phase IIV clinical trials).

We are particularly interested in candidates who have led or supportedrheumatologyclinical programs and who are comfortable serving as the study physician providing medical monitoring oversight (e.g. safety review contribution to protocol development including study design endpoints and eligibility criteria) and working collaboratively with other project team addition to strong scientific leadership the role is expected to be highly client-facing with an increased business development component - requiring regular engagement at executive level and the confidence and polish to represent Fortrea with senior client leaders external partners and other key stakeholders.

WHAT YOU WILL DO

• High level Medical TA and Clinical Trial Subject Matter Expertise (SME) contributions(maybeRegionalor Global).
• SME Cross-functional scientific & technical contributions and interactions with Clients Medical teams Project teams Key Opinion Leadersand at Principal Investigator/Site levels.
• Partner with clients and internal teams to support business development - shaping clinical/medical strategy for proposals biddefences and client discussions.
• Provide oversight of medical monitoring activities to ensure timelines and quality of medical deliverables and assigns physician resources as required.
• According to the scope of work may serve as Global Lead Regional or Program Project Physician across multiple indications.
• Provide subject matter and drug development expertise and is a key contributor to the medical strategy and execution of the study/program for the client.
• Provides input review and revision of protocols case report forms training materials project specific tools analysis plans design clinical trial reports and new drug applications.
• Prepares materials for and actively participates in investigator meetings and assists at site initiation visits.
• Provides medical/scientific expertise to project team.
• And any other duties as required or assigned.

YOU NEED TO BRING

Qualifications (Minimum Requiredand preferred):

• MD Degree
• Board Certification in Internal Medicine
• Specialization in Rheumatologyandbroadertherapeutic experience in autoimmune diseases (AID)
• Preferred:Specific expertise in cell and gene therapy in autoimmune diseases (AID)
• 3 years of substantial knowledge of drug development and extensive clinical research experience within the pharmaceutical/CRO industry (or as a clinical trial investigator)
• Preferred:Industry experience inclusive of clinical trials medical monitoring experience or other relevant clinical development/trial experience at a CRO pharmaceutical company regulatory agency
• Strong scientific communication and clientfacing capabilities including presenting scientific expertise supporting proposals and strengthening externalpartnerships
• English language skills: Full professional proficiency

Work Environment

• Remote position based in USA
• Occasional national and international travel required including attendance at sponsor meetings investigator meetings and relevant scientific or industry conferences.

Physical Requirements

• Frequently stationary for 6-8 hours per day.
• Repetitive hand movement of both hands with the ability to make fast simple repeated movements of the fingers hands and wrists.
• Occasional crouching stooping with frequent bending and twisting of upper body and neck.
• Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
• Regular and consistent attendance.
• Varied hours may be required.

Pay Range:USD $240000-$340000

Benefits:All job offers will bebased on a candidates skills and prior relevant experience applicabledegrees/certificationsas well as internal equity and market -timeor part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical Dental Vision Life STD/LTD 401(K) Paid time off (PTO) or Flexible time off (FTO) Company bonus where applicable.

Application Deadline: August 30 2026

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