Medical Affairs Review and Approval Expert
Vor 7 Tagen
Medical Affairs Review and Approval Expert (M/F/d)
This is what you can look forward to:
The Medical Affairs Review and Approval Expert (MARA Expert) is part of a team responsible for the medical review and approval of promotional and non-promotional materials across the different Business Units (BU) at Pfizer Switzerland and for corporate and social media materials. This position comes with high responsibility and aims to minimize compliance risks for the company while being the Point of Contact for the approval of materials, communications and documents as outlined below. The role also supports with medical aspects of lifecycle portfolio management.
ROLE RESPONSIBILITIES
- Is a key contributor to ensure local promotional compliance, particularly with regards to local requirements and company procedures.
- Review and/ or approval of promotional and non-promotional materials across different BUs as well as corporate and social media materials in compliance with local regulations and global and local procedures, through the relevant systems, and medical-to-medical processes where appropriate. This also includes reviews of of digital materials and campaigns.
- Ensure scientific accuracy of contents, claims, references, and translations and ensure alignment with local product label information.
- Close collaboration with other Medical Affairs und Commercial colleagues, with content generation stakeholders across different Bus during the whole process of content management to ensure a streamlined approach
- Medical maintenance and lifecycle support and scientific advice for product portfolios, such as medical review of regulatory documents/label updates or management of specific medical requests (e.g. out of stock, pharmacovigilance, specific customer requests medically necessary products, supply questions)
- Training of colleagues in the field of responsibility as applicable
What you offer:
- University degree, as pharmacist, human/veterinary medicines degree, or in life sciences area
- Clinical experience or pharmacy office practice as a strong advantage
- Experience in medical affairs, regulatory affairs or in other similar pharmaceutical positions preferred
- Interest in legal and regulatory aspects of promotional compliance
- Swift familiarization with different therapeutic areas and scientific content
- Ability to collaborate with different teams and to prioritize according to needs
- Ability to understand applicable (local) regulations, Codes of Practice, specifically on promotional compliance, and digital directives
- Good understanding of omnichannel orchestration, digital processes, and social media
- Digital Affinity, sound user skills of IT-processes
- Language Skills: Full fluency in German and English needed.
- French knowledge necessary, Italian as an advantage
- Quality and Compliance mindset
- Ability to maintain focused and manage multiple projects without losing sight of relevant details
- Accuracy, structured way of working, methodological understanding
- Good communication skills,
- Collaborative business acumen, Team spirit and interest in collaboration with local and global teams
- Ability to work independently with high accountability
- Solution driven and quality orientation
- Agility in a transformational environment, Speaking Up attitude and assertiveness
What we offer:
- An attractive overall employment package (compensation, vacation, pension) in a world-leading company
- An exciting, fast-paced environment
- Friendly, open and collaborative company culture
- Being part of a local as well as an interdisciplinary team
- Flexible working hours
- Opportunities to engage in social projects
- Company-paid health activity program
- Great growth
- and development opportunities
- Health programs for all employees
- The opportunity to engage in social projects
Convinced?
LI-PFE
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