Senior Medical Writer (Oncology)

Position Overview: As a Senior Medical Writer in the Clinical Communications team, you will be a pivotal player in crafting high-quality, scientifically accurate content aimed at educating oncology care providers. Your work will directly contribute to improving patient care outcomes in the field of oncology. You will collaborate closely with a Scientific Director (SD) and an internal team to develop content across various mediums, including print, digital, video, and live events. 

Key Responsibilities: 

• Content Development: 

• Perform extensive literature reviews on various disease states, therapeutic advancements, and clinical data. 

• Develop high-quality medical and scientific content for print, digital, video, and event deliverables targeted at oncology professionals. 

• Create content that is aligned with the strategic objectives of the activity, including manuscripts, slide decks, discussion guides, and video-based educational tools. 

• Ensure the scientific and clinical accuracy of all content through a global fact-check of referenced literature and appropriate annotation following AMA style (11th edition) and in-house guidelines. 

• Review and edit content at multiple stages, ensuring consistency, accuracy, and relevance for the target audience. 

• Independently address and incorporate feedback from clients, peer reviewers, and faculty authors throughout the content development process. 

• Collaborate with creative services to ensure that revisions and appropriate changes are addressed within the scope of the project. 

• Collaboration and Communication: 

• Work closely with cross-functional teams to ensure project success, communicating effectively with internal professional services, clients, and key opinion leaders. 

• Regularly interface with internal teams, clients, and faculty during meetings and project discussions. 

• Compliance and Review Process: 

• Support the preparation of materials for pharmaceutical promotional review processes, ensuring compliance with submission requirements. 

• Revise content as needed through its internal and external reviews during the project lifecycle, adhering to medical/legal/regulatory (MLR) review process requirements. 

• Medical Event Attendance: 

• Attend live events such as professional conferences, advisory boards, and video productions to capture key content for project deliverables. 

• Produce high-quality editorial materials, such as executive summaries, articles, and presentations, based on event coverage. 

• Management and Mentorship: 

• Support and train direct reports to independently accomplish all essential roles and responsibilities described above. This will require supplying accurate precise di