This dynamic role in medical communications is for you if you're eager to partner with clients, editors, and scientific directors. You will generate content outlines that contain a clearly highlighted story arc and a complete reference list. We look forward to you organizing and annotating references in accordance with client’s directives or house style.
The Associate Director, Sr. Medical Science Liaison is responsible for cultivating strong scientific relationships with external experts, delivering clinical and scientific insights, and serving as a strategic partner to both internal teams and the broader medical community. The Sr. MSL will build trusted partnerships with key opinion leaders (KOLs), facilitate scientific exchange, and collaborate cross-functionally to advance internal initiatives. This role is critical in supporting strategy through targeted patient identification efforts.
This critical role will ensure the medical integrity, topicality and timeliness of the content for client projects and help ensure compliance across Medical and Legal.The Medical Director is responsible for providing medical expertise to clients and internal teams while leading strategy and developing medical content.
The Clinical Documentation and Process Specialist works in partnership with Clinical Development study teams to maintain the eTMF and other clinical systems, optimize processes, track compliance and training activities, develop and report KPIs/metrics, and ensure audit readiness, reporting to the Vice President, Clinical Development.
The Principal Strategic Medical Writer is responsible for leading and writing clinical and regulatory documents that support the company's objectives. The writer independently writes most clinical and regulatory documents within their remit and works closely with teams on document authoring and content strategies to ensure alignment with project goals. The writer contributes to project management strategies driving toward submission objectives.