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Medical Director (Early Phase)

3+ years
Not Disclosed
10 April 24, 2025
Job Description
Job Type: Full Time Education: MD/DO 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 (Early Phase)

Location: San Antonio, TX or Raleigh, NC (Hybrid: Office/Remote)

About ICON plc:
ICON plc is a global leader in healthcare intelligence and clinical research. We are committed to fostering a culture that values inclusion, innovation, and performance excellence. Our teams work collaboratively to shape the future of clinical development and accelerate the delivery of cutting-edge therapies to patients worldwide.

Role Summary:
We are hiring a Medical Director (Early Phase) to provide strategic medical oversight and leadership across Early Phase clinical trials. In this role, you will partner with global cross-functional teams to drive clinical trial success, ensure subject safety, and maintain scientific integrity in trial execution.

Key Responsibilities:

  • Provide expert medical and scientific oversight for Early Phase clinical trials.

  • Ensure subject safety and integrity of trial data through vigilant medical monitoring.

  • Collaborate closely with clinical operations, safety, and regulatory teams to ensure successful execution of clinical studies.

  • Author and review key study documents including clinical protocols, study reports, and regulatory submissions.

  • Interpret clinical data, provide strategic insights, and support evidence-based development decisions.

  • Represent the medical function in internal and external meetings and communications.

Qualifications:

  • Medical Degree (MD or DO) is required.

  • Substantial experience in clinical research and development, ideally with prior involvement as a Principal Investigator for Early Phase trials.

  • Clinical practice experience, preferably in general medicine.

  • Strong preference for candidates with medical monitoring experience.

  • In-depth understanding of clinical trial methodology, regulatory requirements, and GCP guidelines.

  • Demonstrated leadership, collaboration, and decision-making skills in cross-functional, global environments.

  • Superior communication skills and the ability to convey complex medical concepts clearly to stakeholders.

Work Arrangement:

  • Hybrid: Combination of remote and on-site work depending on proximity to ICON’s San Antonio or Raleigh offices.

Compensation & Benefits:

  • Competitive compensation structure.

  • Extensive annual leave entitlements.

  • Comprehensive health insurance packages tailored to individual and family needs.

  • Retirement planning options to secure long-term financial goals.

  • Global Employee Assistance Programme (LifeWorks) available 24/7 for emotional, mental, and physical support.

  • Life assurance and flexible benefit programs, including:

    • Childcare vouchers

    • Bike-to-work schemes

    • Discounted gym memberships

    • Subsidized public transport

    • Health and wellness assessments

Diversity & Inclusion:
ICON is an equal opportunity employer committed to creating an inclusive and accessible workplace. We value diversity and ensure fair consideration for all applicants regardless of race, color, religion, gender, sexual orientation, national origin, disability, or veteran status.