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Associate Medical Director/Med Dir - Neurology

1-2 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

Associate Medical Director / Medical Director – Neurology (Fully Remote, US-Based)

Category: Clinical Research
Job Type: Full Time
Job ID: R-01323565
Work Model: Fully Remote (United States Only)

Thermo Fisher Scientific’s PPD clinical research portfolio continues to lead the global CRO sector through high-quality scientific expertise, rigorous medical oversight, and world-class clinical trial operations. As part of our Clinical Research team, you will contribute to advancing therapies that address the world’s most complex neurological and medical challenges.

This role supports end-to-end clinical trial execution, medical monitoring, pharmacovigilance oversight, and safety evaluation across drug development programs. Candidates must be legally authorized to work in the United States without sponsorship.


Position Overview

The Associate Medical Director / Medical Director – Neurology provides medical oversight for clinical trials, ensuring adherence to GCP, ICH guidelines, industry regulations, and client requirements. The role includes safety data evaluation, medical leadership for study teams, clinical consultation, regulatory documentation review, and contribution to pharmacovigilance deliverables.

You will collaborate closely with cross-functional teams, investigators, regulatory bodies, and sponsors to ensure high-quality clinical and safety outcomes across therapeutic programs.


Key Responsibilities

Medical & Clinical Trial Leadership

  • Provide medical oversight and leadership for assigned clinical studies across all phases of development.

  • Ensure medical, scientific, and ethical integrity of clinical trials and adherence to study protocols.

  • Serve as medical consultant to clients, investigators, project teams, and internal stakeholders.

  • Present medical and safety content at investigator meetings and sponsor engagements.

  • Deliver therapeutic and protocol training for clinical team members.

Safety & Pharmacovigilance Oversight

  • Conduct medical review of serious adverse events, adverse events of special interest, clinical outcomes, and safety narratives.

  • Evaluate safety signals, review aggregated safety reports, and support label updates and risk management activities.

  • Review ICSRs, PBRERs, PSURs, DSURs, REMS, RMPs, CTD modules, and related regulatory documentation.

Regulatory & Scientific Contributions

  • Interpret and analyze clinical and safety data for regulatory submissions, CSRs, IND/NDA components, and other scientific outputs.

  • Collaborate with cross-functional teams to ensure timely and accurate delivery of medical content.

  • Support business development activities when required.


Experience Level

  • Associate Medical Director:

    • MD with formal Neurology training (residency and/or fellowship)

    • Minimum 2 years of patient treatment experience

    • 1–2 years of clinical trial, CRO, PV, or industry experience

  • Medical Director:

    • MD with formal Neurology specialization

    • Minimum 2 years of patient treatment experience

    • 2+ years of industry experience in clinical development, medical monitoring, or pharmacovigilance

    • Candidates with expertise in Neuromuscular or Pediatric Neurology preferred


Required Qualifications

  • MD or equivalent; active medical license preferred.

  • Strong clinical competence in Neurology with proven clinical training and patient care experience.

  • Experience in clinical development, medical monitoring, clinical trials, or pharmacovigilance.

  • Understanding of FDA, EMA, ICH, and GCP guidelines.

  • Proficiency with safety databases and medical coding tools (e.g., MedDRA).

  • Strong analytical, decision-making, and communication skills.

  • Ability to work independently in a fast-paced, matrixed, and global environment.

  • Excellent written and verbal English communication.


Key Skills

  • Therapeutic expertise in Neurology

  • Safety data evaluation

  • Clinical decision-making

  • Cross-functional collaboration

  • Data interpretation and medical writing

  • Risk assessment and mitigation

  • Problem solving and stakeholder communication


Work Environment & Physical Requirements

  • Office-based remote environment with use of standard office technology.

  • Frequent periods of 6–8 hours of computer-based work.

  • Ability to travel domestically and internationally as required.

  • Occasional lifting of items up to 20 lbs (e.g., laptop, luggage).

  • Regular interaction with diverse internal and external teams.


Benefits

Thermo Fisher Scientific offers a comprehensive compensation package, including competitive salary, annual incentive bonus, healthcare coverage, retirement benefits, paid time off, and extensive career development programs. You will join an organization committed to innovation, integrity, and scientific excellence.