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Medical Director/Clinical Trial Physician - Endocrinology(Remote U.S)

1-3 years
Not Disclosed
10 June 3, 2025
Job Description
Job Type: Remote Education: MD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title

Medical Director / Clinical Trial Physician – Endocrinology

Location

Remote – United States (ideally located in Eastern or Central Time Zones)
Job ID: R-01311546
Job Type: Full-time
Work Schedule: Monday–Friday
Work Environment: Fully Remote


Company Overview

Thermo Fisher Scientific’s PPD® clinical research portfolio supports global drug development through laboratory, digital, and decentralized clinical trial services. This role supports the advancement of therapies in endocrinology by providing medical oversight for clinical trials.


Role Summary

Serve as a medical leader and trial physician for endocrinology-focused clinical trials. Responsibilities include protocol development, medical monitoring, regulatory support, and stakeholder communication. The position collaborates across internal teams and external stakeholders to ensure high-quality trial execution and subject safety.


Key Responsibilities

  • Provide medical leadership throughout clinical trial design and execution

  • Develop and review protocols, CSRs, ICFs, CRFs, and other clinical documents

  • Conduct real-time medical monitoring for subject safety and protocol adherence

  • Interpret clinical trial data and contribute to regulatory documents and publications

  • Serve as medical point of contact for investigators, IRBs, and regulatory bodies

  • Ensure medical compliance with SOPs and GCP standards

  • Train site staff and internal teams (e.g., CRAs)

  • Collaborate with study teams to assess risks, resolve issues, and ensure harmonized decisions

  • Represent the study in executive or safety review boards, as needed


Education and Experience

  • Medical Doctor (MD) or equivalent degree required

  • Board certification in Endocrinology strongly preferred

  • Clinical background with patient treatment and/or research experience in endocrinology

  • 1–3 years of industry experience in a pharmaceutical, biotech, or CRO environment


Knowledge, Skills, and Abilities

  • Experience with NDA submissions and regulatory documentation

  • Strong knowledge of adverse event reporting regulations

  • Proven leadership and interpersonal skills for working in cross-functional teams

  • Strong written and verbal communication in English

  • Ability to work effectively in global, matrixed organizations

  • Conflict resolution and problem-solving capabilities

  • Able to handle confidential and sensitive medical data with accuracy

  • Willingness to travel 10–20%, including internationally


Physical and Technical Requirements

  • Frequent stationary work (6–8 hours/day)

  • Occasional domestic/international travel

  • Ability to lift up to 15–20 lbs (e.g., laptop, luggage)

  • Use of common office and clinical trial software

  • Requires multitasking, concentration, and independent work


Compensation and Benefits

  • Competitive base salary and annual incentive plan bonus

  • Comprehensive benefits package, including:

    • Medical, dental, vision insurance

    • 401(k) retirement plan

    • Paid time off, holidays, and parental leave

    • Tuition reimbursement

    • Employee Stock Purchase Plan (ESPP)

More information: Thermo Fisher Total Rewards