Proclinical is working alongside a pharmaceutical company seeking a Global Dir.
Med.
Comms & Pubs.
In this role, you will lead the development and execution of med.
comms.
and pub.
plans across North America, Europe, and Asia.
You will ensure alignment with corporate strategy, global comms., and marketing, and work closely with SMEs and key opinion leaders (KOLs).
This is a remote role in Europe.
Responsibilities: Develop and execute data-driven medical content and publications.
Collaborate with Medical Affairs, Clinical Development, and Medical Science Liaisons to create medical education materials.
Ensure content aligns with healthcare practitioner needs and global communications.
Maintain scientific and clinical accuracy across all deliverables.
Manage multiple projects across departments effectively.
Lead content review processes to meet stakeholder needs.
Serve as a liaison between Medical Affairs and Clinical Development teams.
Oversee the planning and execution of medical and scientific publications.
Ensure publications adhere to industry standards and company policies.
Create strategic medical communication and publication plans.
Develop publication planning and editorial services.
Identify and engage Key Opinion Leaders for authoring and participation.
Manage event content for scientific meetings, advisory boards, webinars, and symposia.
Develop disease-awareness programs and training materials.
Produce interactive media and translation programs from clinical data to practice.
Key Skills and Requirements: Bachelor's degree in a scientific discipline; advanced degree/license preferred (Master, MD, PharmD, RPh, Ph.D.).
Extensive experience in publications and medical writing within the biotech/pharmaceutical industry, with a focus on oncology or nuclear medicine.
Strong interpersonal, negotiation, communication, and collaborative skills.
Ability to write and edit scientific manuscripts, posters, and abstracts.
Proficiency in creating and editing medical illustrations.
Knowledge of Medical Affairs, Clinical Development, and Regulatory functions.
Familiarity with relevant guidelines (GPP3, ICMJE), laws, and industry best practices.
Proficiency with Microsoft Office tools.
Exceptional attention to detail and organizational skills.
Ability to work across multi-disciplinary groups and lead decision-making discussions.
Creative problem-solving skills and a consumer-focused mindset.
Fluency in English (written and spoken).
If you are having difficulty in applying or if you have any questions, please contact Jake Robinson at ****** Apply Now: If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV.
Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.
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Proclinical is acting as an Employment Agency in relation to this vacancy.