The Copy Supervisor is responsible for developing high-quality clinical, market access, and patient engagement copy while ensuring accuracy and adherence to regulatory standards. They will lead creative projects, mentor junior staff, and collaborate cross-functionally with medical and account teams to drive brand strategy.
Plan and execute promotional pharmaceutical speaker bureau events from start to finish, coordinating speakers, travel, venues, attendees, technology, and event materials. Serve as the primary contact for client field teams and healthcare professionals while ensuring compliant closeouts, accurate reporting, and strong program performance.
The Meeting Coordinator will manage end-to-end registration processes, including building registration sites and maintaining attendee data for pharmaceutical meetings. They will also support backend program logistics, budget tracking, and onsite event execution to ensure programs run smoothly.
Fellows will develop core competencies in medical communications by creating scientific content while working cross-functionally with internal and external stakeholders. They will gain hands-on experience in medical writing and scientific strategy while adhering to industry guidelines and publication practices.
The Senior Medical Writer is responsible for researching, writing, and editing high-quality scientific content for medical communications initiatives. They must manage project timelines, collaborate with stakeholders, and ensure all deliverables meet ethical and editorial standards.
The Scientific Director provides strategic scientific and publications oversight across multiple accounts, ensuring scientific accuracy and adherence to client preferences. They also lead the development of scientific content, mentor internal team members, and serve as a strategic thought partner for clients.
