Senior Director - Global Medical Information & Medical Affairs
Senior Director - Global Medical Information & Medical Affairs
Senior Director - Global Medical Information & Medical Affairs
Senior Director - Global Medical Information & Medical Affairs
Proclinical Staffing
Pharma, Medizintechnik
Zürich
- Art der Anstellung: Vollzeit
- Hybrid
Senior Director - Global Medical Information & Medical Affairs
Über diesen Job
Senior Director - Global Medical Information & Medical Affairs
- Job type: Permanent
- Discipline: Medical Information
- Location: Switzerland
Looking to escape your long commute to work? Are you a Medical Affairs Professional? Unlock your new remote working position with this exciting role!
Proclinical is seeking a Senior Director to lead Global Medical Information and Medical Affairs operations within the radiopharmaceuticals space. In this role, you will oversee medical information processes, manage investigator-initiated studies, and provide strategic medical input across international markets. This is an exciting opportunity to make a global impact in a high-growth, science-driven environment.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
- Lead the Medical Information department, managing standard responses and addressing medical queries from subsidiaries, distributors, and healthcare professionals.
- Develop and deliver scientific communication materials, including medical writing, slide decks, abstracts, posters, presentations, and manuscripts.
- Provide strategic medical insights to business, marketing, and Real-World Evidence teams.
- Support regulatory affairs by contributing to clinical updates and committee activities.
- Oversee Investigator-Initiated Studies (IIS), Compassionate Use (CU), and Named-Patient Programs (NPP).
- Train and support internal teams, including sales and medical affairs staff, on radiopharmaceuticals and nuclear medicine procedures.
- Monitor departmental performance using KPIs and drive continuous process improvements.
Key Skills and Requirements:
- Advanced degree (MD, PharmD, or PhD) with expertise in the pharmaceutical industry, particularly in radiopharmaceuticals or nuclear medicine.
- Strong background in medical information, medical writing, and global medical affairs.
- Comprehensive knowledge of nuclear medicine and oncology.
- Familiarity with EU, North American, and ICH regulations in clinical development and pharmacovigilance.
- Proficiency in tools such as Excel, Word, PowerPoint, SharePoint, and Veeva.
- Excellent written and verbal communication skills in English.
If you are having difficulty in applying or if you have any questions, please contact Tom Pinnock at t.pinnock@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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