Senior Medical Director, Medical Affairs (Oncologist) - U.S. Remote

3-6 years

Not Disclosed

United States

10 March 6, 2025

Job Description

Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Senior Medical Director, Medical Affairs (Oncologist) – U.S. Remote

Employer: Worldwide Clinical Trials - USA
Location: Remote (United States) – North Carolina preferred
Salary: Competitive
Start Date: March 5, 2025
Closing Date: April 4, 2025

Who We Are:

Worldwide Clinical Trials is a global, midsize CRO that pioneers innovative solutions in clinical research. With a team of over 3,500 experts, we challenge conventional approaches to advance treatments for some of the world’s most persistent diseases.

What Medical Affairs Does at Worldwide Clinical Trials:

Medical Affairs plays a crucial role throughout the clinical trial lifecycle, from business development to regulatory submissions. The team collaborates across multiple functions, contributing to study design, feasibility assessments, medical monitoring, pharmacovigilance, and medical writing.

Key Responsibilities:

Provide medical oversight for oncology clinical trials as Medical Monitor and, when applicable, Global Lead Medical Monitor.
Conduct medical data review to ensure integrity, accuracy, and quality of clinical trial data.
Work closely with pharmacovigilance teams on Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs).
Contribute to the design and execution of clinical development programs, study protocols, and research materials.
Deliver protocol-specific and therapeutic training to project teams.
Support business development through feasibility assessments, proposal generation, budget development, and sponsor engagement.
Mentor junior medical staff, demonstrating strong ethics, compassion, and integrity.
Stay updated on therapeutic and regulatory advancements through conferences, literature reviews, and internal discussions.

Requirements:

Medical Degree with board certification in oncology.
Fellowship training in medical oncology, including malignant hematology.
3-6 years of medical monitoring experience, preferably in a CRO, pharmaceutical, or biotech setting.
Strong expertise in medical data review and ensuring data quality.
Excellent organizational, communication, and presentation skills (Word, Excel, PowerPoint).
Ability to manage multiple priorities and collaborate within matrixed study teams.
Availability to travel domestically up to 20% and provide after-hours medical support when needed.

Why Join Us?

Best-in-class industry pay and benefits.
A collaborative, inclusive work environment with a strong learning curve.
Work alongside experts in clinical research, making a direct impact on patient lives.
Opportunities for career growth in a mission-driven organization.

Join Worldwide Clinical Trials and be part of the future of oncology research!

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Senior Medical Director, Medical Affairs (Oncologist) - U.S. Remote

Job Description

Who We Are:

What Medical Affairs Does at Worldwide Clinical Trials:

Key Responsibilities:

Requirements:

Why Join Us?

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