The Senior Program Manager will lead the execution of medical communication publication projects by managing timelines, budgets, and cross-functional team collaboration. They will serve as the primary point of contact for clients, ensuring all deliverables meet strategic objectives and quality standards.
The Associate Medical Director assists senior scientific staff in developing scientifically accurate and strategically sound medical communications content. Responsibilities include synthesizing clinical trial data, managing client projects, and providing expert scientific support across medical affairs and publications.
The Medical Writer will interpret preclinical and clinical research data to create high-quality scientific written materials for pharmaceutical clients. They will also participate in client meetings and stay current with medical developments to ensure the accuracy of all project deliverables.
