Zenith LifeScience

Title: Contractor – Medical Education & Training, Oncology

Location: Nutley, NJ

Specialties: Oncology

Summary

Supports the Oncology Medical Communications team by developing and reviewing compliant scientific exchange materials for use by Global and US Medical Affairs. Responsibilities include creating internal and external medical resources such as MSL slide presentations, advisory board materials, training modules, congress reports, and other scientific exchange resources. Collaborates cross-functionally and ensures content accuracy and alignment with Medical Communications strategy. Manages workflow and reference library, conducts literature reviews, and integrates new information into resources.

Added on: 08/21/2025

Full Job Description

Job Description:

Contractor, Medical Education & Training - Oncology, will support the Oncology Medical Communications team and is responsible for development of medical communications deliverables for use by Global and US Medical Affairs, aligned with the Medical Affairs strategic plan for assigned therapeutic area(s). These deliverables include development and review of compliant scientific exchange materials to be used in external interactions with KOLs (i.e. by MSLs), advisory boards, congress reports, internal medical affairs strategic communication tools (i.e. medical narratives) and other internal medical affairs training and education materials (i.e. core MA training modules). The contractor will work cross-functionally with the broader Medical Affairs team as appropriate.


Essential Functions

Development of high-quality internal and external medical resources, including reactive/proactive MSL slide presentations, advisory board materials, internal training materials, congress reports, and other scientific exchange resources Ensure development of scientific content is relevant, accurate, and aligns with the Medical Communications strategy Collaborate closely with cross-functional teams to ensure alignment on deliverables Conduct literature reviews and stay updated on latest publications to integrate new information into existing resources Follow appropriate review and approval processes according to Company policies and procedures Workflow task management and tracking of multiple projects Reference library management, including keeping up with published literature, uploading key papers and congress materials to library, maintaining reference library catalog, and updating training guides


Requirements:

Advanced scientific or medical degree (PhD, PharmD, or MD) required. Research or work experience in oncology preferred. At least 2 years of medical writing or content development experience preferred. At least 2 years of experience in pharmaceutical industry preferred Proficiency in VEEVA VAULT Experience with advisory board content development and writing topline or executive summary reports Strong analytic skills with the ability to distill complex topics in a timely, effective manner including data analytics (data visualization platforms) experience preferred. Strong understanding of medical content creation to create high-quality content that is accurate, informative, engaging, and innovative. Strong collaborative nature and overall written and verbal communication skills. Demonstrated ability to think critically, balance multiple priorities, analyze situations and achieve goals Strong attention to detail Proficiency with Microsoft Office Suite