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

3-6 years
Not Disclosed
10 Feb. 11, 2025
Job Description
Job Type: Full Time Education: M.D. 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: Virtual (North Carolina, United States – Remote)
Salary: Competitive
Start Date: 8 Feb 2025
Closing Date: 10 Mar 2025


About Worldwide Clinical Trials

At Worldwide Clinical Trials, we are a global midsize CRO that pioneers groundbreaking research to combat some of the world’s most persistent diseases. Our team of 3,500+ experts is dedicated to pushing boundaries and transforming clinical research with innovative approaches that prioritize quality and excellence.

We seek individuals who share our passion for improving lives and thrive in an environment where creativity, collaboration, and inclusion are at the forefront.


The Role of Medical Affairs

Medical Affairs is a critical part of our clinical trial process, providing scientific and medical oversight from Business Development to Regulatory Submissions. Our team supports projects with expertise in:

  • Protocol preparation & feasibility assessments
  • Medical monitoring & pharmacovigilance
  • Training site staff & clinical teams
  • Medical data review & regulatory compliance

As a Senior Medical Director, Medical Affairs (Oncology), you will play a key leadership role in ensuring the safety, quality, and scientific integrity of our oncology trials.


Key Responsibilities

  • Provide medical oversight for oncology clinical trials, serving as Medical Monitor or Global Lead Medical Monitor.
  • Conduct medical data reviews to ensure the accuracy, consistency, and integrity of clinical trial data.
  • Collaborate with pharmacovigilance teams on safety reporting, including Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs).
  • Contribute to the design and execution of clinical development programs, including protocol development and research materials.
  • Provide protocol-specific and therapeutic training to project teams.
  • Support business development by conducting feasibility assessments, generating proposals, developing budgets, and engaging with sponsors.
  • Mentor and guide junior medical staff, fostering a culture of ethics, compassion, and integrity.
  • Stay up-to-date with therapeutic and regulatory advancements by attending conferences, reviewing literature, and participating in internal discussions.

What You Bring to the Role

  • Medical Degree (M.D.) with board certification in oncology.
  • Fellowship training in medical oncology, including malignant hematology (required).
  • 3-6 years of medical monitoring experience, preferably within a CRO, pharmaceutical, or biotech setting.
  • Strong expertise in medical data review, clinical trial oversight, and regulatory compliance.
  • Proficiency in Microsoft Word, Excel, Access, and PowerPoint.
  • Exceptional organizational, communication, and presentation skills.
  • Ability to manage multiple priorities and collaborate effectively within matrixed study teams.
  • Availability for domestic travel (up to 20%) and flexibility for after-hours medical support when needed.

Why Join Us?

At Worldwide Clinical Trials, we believe in empowering our team through:
✔ A collaborative and inclusive work environment.
✔ Opportunities to lead and innovate in oncology research.
✔ Direct involvement in transformative clinical trials impacting patient lives worldwide.

We love knowing that the work we do improves lives every day.

Apply today to be part of our mission!

Visit our careers page to explore more opportunities.

Worldwide Clinical Trials is an equal opportunity employer, committed to diversity, inclusion, and equal access to opportunities for all applicants.