Medical Review Manager focused on compliance and strategic opportunities in promotional materials for Pfizer. Collaborating across teams to ensure high compliance standards in Denmark and Norway.
Responsibilities
Act as the single point of contact for Medical Review, enabling efficient review processes for both promotional/ non-promotional and Medical-to-Medical materials.
Identify and assess strategic opportunities for in-country service and operations improvements.
Collaborate with cross-functional and cross-country teams to build consensus and influence decision-making.
Acquire and maintain in-depth scientific knowledge of Pfizer medicines within nominated therapy area(s), including those in development.
Independently perform fact-check, scientific review and medical approval of promotional and medical materials and activities in line with local product label information, country-specific code and regulatory requirements.
Provide specialist medical, scientific and code/regulatory advice to teams during the development phase of materials/projects/activities.
Provide advice that will ensure that the highest ethical standards are upheld, and that Pfizer always remains compliant with regulations.
Develop and sustain constructive, continuous improvement focused relationship with leadership and stakeholders.
Manage local code/regulatory complaints and intracompany dialogue to the extent required and advise on corrective and preventative actions.
Requirements
University degree (Bs., Ms., PhD) in a relevant field (Pharmacy and Medicine preferred)
Skilled in local Danish regulations regarding medical information
4-6 years of experience in medical review, compliance or related roles
Strong understanding of local and global regulations
Fluent in Danish and in English is required. Norwegian or other languages will be considered an advantage.
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