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Sr Med Director - Hematology/Oncology(Remote U.S)

12+ 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

Sr. Medical Director – Hematology/Oncology

Location

Remote (U.S.-based; listed in Texas, but open nationwide)
Job ID: R-01312310
Job Type: Full-time
Work Schedule: Monday–Friday
Work Environment: Fully Remote


Company Overview

Thermo Fisher Scientific, through its PPD® clinical research portfolio, provides industry-leading clinical research services. This role sits within the Pharmacovigilance (PV) team, responsible for drug safety, medical strategy, regulatory compliance, and global medical oversight in clinical trials.


Role Summary

This senior medical leadership role provides strategic and operational oversight of global PV activities, with a therapeutic focus in hematology and oncology. Responsibilities include medical review of safety data, internal and external leadership, regulatory compliance, process improvement, and team mentoring.


Key Responsibilities

  • Provide leadership, mentorship, and strategic direction within the PV physician team

  • Serve as primary medical contact for clients and internal teams

  • Oversee clinical safety deliverables (e.g., SAE reviews, aggregate reports, risk management documents)

  • Guide business development strategy and contribute to proposals

  • Represent PV during audits, inspections, and regulatory interactions

  • Develop and manage budgets and resource allocation

  • Participate in recruiting and onboarding activities

  • Collaborate across departments to align goals and ensure compliance


Education and Experience

  • MD or equivalent required

  • Board certification in Hematology or Oncology highly preferred

  • Minimum 12 years of relevant experience, including:

    • At least 2 years of clinical care in a related specialty

    • At least 5 years of industry or clinical trial experience in a CRO, pharma, or academic setting


Knowledge, Skills, and Abilities

  • Therapeutic expertise in hematology/oncology drug development

  • Strong understanding of global PV regulations (FDA, EMA, etc.)

  • Leadership in safety operations and medical monitoring

  • Proficiency in safety data interpretation and regulatory submission standards

  • Excellent written and verbal communication

  • Strong decision-making, organizational, and mentoring skills

  • Ability to manage global teams and influence key stakeholders

  • Willingness to travel domestically and internationally (10–20%)


Physical and Technical Requirements

  • Ability to work independently in a remote environment

  • Frequent stationary work; ability to travel occasionally

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

  • Use of various clinical and office software systems


Compensation and Benefits

  • Competitive base salary with annual incentive bonus eligibility

  • Comprehensive benefits package including:

    • Medical, dental, vision coverage

    • 401(k) with company match

    • Paid time off and holidays

    • Paid parental leave

    • Employee Stock Purchase Plan (ESPP)

    • Tuition reimbursement and wellness programs

More information: Thermo Fisher Total Rewards