Job Title
Medical Director / Global Medical Indication Lead – Nephrology (FSP)
Location
Remote – United States (Eastern or Central Time Zone preferred)
Job ID: R-01308355
Job Type: Full-time
Work Environment: Fully Remote
Work Schedule: Standard (Monday–Friday)
Travel: 10–20% (including possible international travel)
Company Overview
Thermo Fisher Scientific, through its PPD® clinical research services, is a global leader in contract research and drug development. This role supports a growing Functional Service Provider (FSP) team, focused on Nephrology, enabling patient-centered research strategies across multiple studies.
Role Summary
The Medical Director / Global Medical Indication Lead – Nephrology is a senior strategic leader within the FSP program, responsible for the full clinical development lifecycle of nephrology studies. This includes translating the Target Product Profile (TPP) into a robust Clinical Development Plan (CDP), leading cross-functional study teams, ensuring medical oversight, and harmonizing study execution across global trials.
Key Responsibilities
Strategic Leadership & Planning
Lead the Clinical Development Plan (CDP) for the Nephrology indication in alignment with asset strategies.
Provide ongoing strategic and clinical insights during all phases of drug development (Phase I–Registration).
Lead indication-specific medical advisory boards and strategy planning.
Medical Oversight & Study Harmonization
Oversee the medical aspects of all active nephrology studies, ensuring real-time communication and coordination.
Guarantee consistency across studies, particularly in responses to IRBs, regulatory authorities, and other stakeholders.
Ensure compliance and timely risk communication to senior management.
Team Leadership & Development
Line-manage and mentor Clinical Trial Physicians working on the indication.
Build and maintain a high-performing team of development medical doctors.
Identify high-potential staff for succession planning and expanded roles.
Qualifications
Education
Medical Doctor (MD) or equivalent required.
Board certification in Nephrology strongly preferred.
Additional specialty education in Immunology or Internal Medicine a plus.
Experience
Minimum 3–5 years in the pharmaceutical or biotech industry with end-to-end clinical trial experience.
Expertise in clinical trial design, interpretation of clinical data, and regulatory expectations.
Experience managing global study teams in a matrixed environment.
Skills
Excellent leadership, coaching, and mentoring abilities in global settings.
Clear, strategic communicator capable of motivating diverse teams.
Strong understanding of cross-study harmonization, risk mitigation, and clinical operations.
Proficiency in English (written and verbal) is required.
Work Environment & Physical Requirements
Office-based (remote), with use of standard office technology
Occasional domestic/international travel (10–20%)
Frequent sitting (6–8 hours), light to moderate lifting (15–20 lbs), and computer use
High concentration and multitasking capabilities required
Compensation & Benefits
Estimated Salary Range (North Carolina): $200,000 – $278,900/year
Eligible for a variable annual bonus based on individual, team, and company performance
Comprehensive Total Rewards package, including:
National medical, dental, and vision plans
PTO (minimum 120 hours/year) + 10 paid holidays
Parental leave, life insurance, disability coverage
401(k) with company match
Tuition reimbursement and Employee Assistance Program (EAP)
Employee Stock Purchase Plan (ESPP)
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