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Medical Director/Clinical Trial Physician - Neurology(Client Dedicated)

1-3 years
Not Disclosed
10 Nov. 27, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Medical Director / Clinical Trial Physician – Neurology (Client Dedicated, Fully Remote – US)

Job ID: R-01303948
Category: Clinical Research
Employment Type: Full-Time
Location: Fully Remote, United States


About the Role

Thermo Fisher Scientific is seeking a Medical Director/Clinical Trial Physician – Neurology (Client Dedicated) to support a global mid-sized biotechnology client focused on innovative autoimmune disease therapeutics. This fully remote U.S. position provides an opportunity to lead high-impact clinical programs, contribute to neurology-focused research, and guide cross-functional study teams across global clinical operations.

This role is ideal for a Neurologist with prior industry experience who wants to drive clinical development, improve patient outcomes, and contribute to breakthrough therapies in a fast-growing scientific environment.


Key Responsibilities

  • Provide medical leadership across clinical study teams, ensuring high-quality and timely clinical trial execution.

  • Lead the development, review, and approval of clinical trial protocols, amendments, CSRs, ICFs, CRFs, and other clinical documentation.

  • Conduct real-time medical monitoring, ensuring subject safety, data validity, and early issue identification.

  • Interpret clinical trial data for regulatory submissions including INDs, NDAs, MAAs, annual reports, manuscripts, and publications.

  • Act as the primary medical point of contact for investigators, IRBs, study sites, internal teams, and health authorities.

  • Participate in medical training for CRAs and site staff; support cross-functional teams in risk identification and mitigation.

  • Ensure compliance with GCP, SOPs, regulatory requirements, and medical governance standards.

  • Collaborate closely with study teams to align on study risks, decisions, and outcomes, ensuring transparent communication.

  • When multiple physicians are assigned, act as a harmonizing medical leader ensuring consistent decision-making across protocols.


Required Education & Experience

  • Medical Doctor (MD) or equivalent degree required.

  • Specialized training in Neurology (residency or fellowship) with relevant patient care and/or research experience.

  • 1–3 years of pharmaceutical, biotech, or CRO industry experience in clinical development is required.

  • Experience supporting Neurology, Pediatric Neurology, or Neuromuscular disorders is highly preferred.

  • Demonstrated experience or understanding of the NDA submission process and regulatory requirements.

  • Must be legally authorized to work in the United States without sponsorship.


Preferred Skills & Competencies

  • Strong command of English, both written and spoken, and ability to travel 10–20 percent (domestic and international).

  • Deep understanding of adverse event reporting and global regulatory guidelines.

  • Proven leadership and interpersonal skills with the ability to guide study teams and collaborate in a cross-functional, global environment.

  • Effective communication abilities to ensure clarity across study plans, risks, and outcomes.

  • Strong problem-solving, negotiation, and decision-making skills with the ability to work in a matrix organizational structure.

  • Ability to manage complex clinical activities with minimal supervision, maintaining accuracy under pressure.


Work Environment & Physical Requirements

  • Remote office-based role with occasional travel to study sites and meetings.

  • Frequent stationary work (6–8 hours/day) with repetitive hand movements.

  • Occasional bending, lifting (15–20 lbs.), and mobility requirements.

  • Frequent communication with diverse teams and stakeholders.

  • Ability to manage multiple tasks, maintain focus, and perform effectively under stress.

  • Regular, consistent attendance required.


Why Join Thermo Fisher Scientific

  • Competitive compensation and annual performance incentives.

  • Comprehensive healthcare and employee benefits.

  • Robust global career development opportunities within a leading clinical research organization.

  • Work culture defined by Integrity, Intensity, Innovation, and Involvement.

  • Opportunity to contribute to groundbreaking science impacting global health.