Senior Medical Reviewer (Temporal 6M)

The Senior Medical Excellence Reviewer will be a key member of the Medical Review Excellence (MRE) Group by acting as a key partner to in-country Medical Affairs and Marketing colleagues.  The Senior Medical Excellence Reviewer role does medical and regulatory review aims to minimize compliance risks by ensuring review and approval of promotional and non-promotional marketing materials as well as Medical to Medical content in conformity with all applicable country law, regulation and industry code. As an active thought leader and medical processes partner, this role will also draw upon best practices to identify new ways of working and drive continuous improvement that generates value for medical colleagues in-country. 

RESPONSIBILITIES 

Strategic oversight:

•    Subject Matter Expert and single point of contact for Medical Review Excellence to enable lightspeed deliverables for Promotional & Medical-to-Medical review objectives for Medical.
•    Identify strategic opportunities for in-country service and operations improvements that align with business priorities & building consensus among cross-functional teams and influence decision making.
•    Gather and analyze in-country metrics focused on MRE utilization and performance; develop compelling and insightful strategic recommendations for leadership and the country.
•    Close partnership with CMAO categories, and country partners to drive active engagement with key Medical and Marketing stakeholders.
•    Leads process documentation and improvement, as applicable.
•    Provides consultation for Marketing and Medical leads in support of compliant content creation as required.

Stakeholder Management:

•    Engages with category Medical and Marketing teams to ensure needs are met for both promotional, medical-to-medical as well as corporate and social media materials in-country.
•    Develops and sustains constructive, continuous improvement focused relationship with leadership and stakeholders.
•    Leads in-country communication with different stakeholders and their departments for a coordinated structure of functions and workflow.

Technical:

·    Act as super-user and change leader who provides in-country medical review and approval services in the designated electronic approval system (to support the appropriate use of Pfizer medicines and successful implementation of Pfizer’s materials, initiatives, and programmes in-country.
·    To 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.
·    To provide solution-focused feedback and recommendations to material owners that enable revisions to be made so that messages in materials ensure the appropriate use of Pfizer medicines and compliance with local code/regulations. 
·    To acquire and maintain scientific knowledge of Pfizer medicines within nominated therapy area(s) (including those in development) as well as of key competitors and national guidelines relevant to the country.
·    To maintain knowledge about local regulations, Pfizer policies relevant to creation and review and approval of materials as well as any additional guidance which may apply to the MRE function.
·    Organize trainings on regulatory requirements and promotional material requirements for relevant colleagues and stakeholders.
·    Ensure handling of complaints related to promotional materials together with the Country Medical Director and local MRE lead.
·    Support local inspections/audit as defined by the local inspection action plan(s) and applicable local audit processes.

Service expansion:

•    Operationalize transformative initiatives: Inception of applicable pilot activities of medical support services and drive them to business as usual, with an enterprise mindset.
•    Processes and workflows developed building efficiencies and value add for the stakeholders.
•    Support in-country execution of opportunities against recommendations quickly and with flawless accuracy.
•    Support in-country cross-functional/country projects and manage BAU transition.
•    Create local operational processes and practices (as needed) that drive efficiencies for the MRE and associated stakeholders.
•    Partner with transformational teams across the organization to support the design and deliver innovation within the CMAO platform with emphasis on the in-country model. 
•    Support international and national congresses to assure they comply with local regulations. 

YOUR PROFILE 

•    Bachelor's Degree / Master's Degree / PhD in Life Sciences field.

•   Previous experience in medical writing / medical revi