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Medical Director/Clinical Trial Physician - Pediatrics

1-3 years
Not Disclosed
10 Nov. 27, 2025
Job Description
Job Type: Full Time 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 – Pediatrics (Remote, US-Based)

Job ID: R-01303954
Job Type: Full-Time
Category: Clinical Research
Location: Fully Remote, United States (Eastern/Central Time Zone Preferred)


About the Role

Thermo Fisher Scientific is seeking an experienced Medical Director/Clinical Trial Physician – Pediatrics to support our global clinical research portfolio within the PPD® clinical research division. This fully remote role provides strategic medical leadership across pediatric clinical trials and contributes directly to advancing life-changing therapies worldwide.

The ideal candidate brings advanced pediatric expertise, proven medical monitoring capabilities, and a strong background in clinical development within pharmaceutical, biotechnology, or CRO settings.


Experience Level Required

  • Experience Required: 1–3+ years in clinical development, medical monitoring, or clinical research within a Pharma, Biotech, or CRO environment

  • Pediatric Clinical Expertise: Residency/Fellowship in Pediatrics required

  • Preferred: Pediatric Neurology, Pediatric Rheumatology, or Rare Disease specialization

  • Senior-Level Medical Expertise: Ability to lead cross-functional study teams and provide high-quality medical oversight


Key Responsibilities

Medical Leadership & Oversight

  • Provide strategic medical leadership throughout clinical trial execution.

  • Develop and review clinical trial protocols, amendments, ICFs, CRFs, CSRs, and regulatory documents.

  • Contribute to site selection and support clinical teams with medical insights.

Medical Monitoring

  • Perform real-time medical monitoring of clinical studies.

  • Ensure medical validity of primary endpoints and subject safety.

  • Identify risks early, escalate issues proactively, and collaborate with the Global Medical Indication Lead.

Regulatory & Scientific Contributions

  • Interpret clinical trial data for regulatory submissions, manuscripts, and publications.

  • Respond to IRB, Health Authority, and investigator queries as needed.

  • Provide medical training to site staff and clinical teams.

Cross-Functional Collaboration

  • Serve as the primary medical point of contact for internal and external stakeholders.

  • Support CRA training, investigator meetings, and study oversight.

  • Ensure alignment across physicians when multiple medical reviewers support a protocol.


Required Qualifications

Education

  • Medical Doctor (MD) or equivalent degree required

  • Board certification preferred

  • Pediatric specialty training (residency/fellowship) mandatory

Professional Experience

  • 1–3+ years of industry experience in clinical development or medical monitoring

  • Experience in pediatric trials strongly preferred

  • Knowledge of regulatory requirements, GCP guidelines, and adverse event reporting

Skills & Competencies

  • Strong clinical judgment and decision-making capability

  • Excellent written and verbal communication skills (English)

  • Ability to collaborate effectively within global, cross-functional teams

  • Proactive problem-solving and negotiation skills

  • Understanding of NDA submission processes and global regulatory frameworks


Work Environment & Physical Requirements

  • Remote U.S.-based position with 10–20% travel, including possible international travel

  • Frequent computer-based work and extended periods of sitting

  • Ability to manage multiple priorities in a fast-paced, global research environment


Benefits & Career Growth

Thermo Fisher Scientific offers competitive compensation and a comprehensive benefits package, including:

  • Health, dental, and vision insurance

  • Annual incentive plan bonus

  • Retirement and savings programs

  • Paid time off, parental leave, and employee support programs

  • Professional development and long-term career opportunities

Join a global organization driven by innovation, scientific excellence, and a mission to make the world healthier, cleaner, and safer.