ROLE SUMMARY
The Internal Medicine – Senior Medical Affairs Advisor / Medical Affairs Manager is responsible for providing medical & scientific support to healthcare professionals and professional bodies through scientific communications and support for clinical research, and for facilitating a medical and scientific bridge between Pfizer and the healthcare community.

We are seeking an Internal Medicine – Senior Medical Affairs Advisor / Medical Affairs Manager to provide specialist medical, scientific and Code compliance advice to the nominated internal team(s) to support the appropriate use of Pfizer medicines and successful implementation of Pfizer’s initiatives and programs.

ROLE RESPONSIBILITIES
Partnerships

• To provide specialist medical and scientific advice to the nominated internal teams to support the appropriate use of Pfizer medicines and successful implementation of Pfizer’s initiatives and programs.
• To provide medical & scientific support to healthcare professionals and professional bodies through scientific communications and support for clinical research to facilitate a medical and scientific bridge between Pfizer and the healthcare community.
• To liaise with healthcare professionals to effectively communicate and manage drug safety issues.
• To build and develop enduring peer-to-peer relationships with leading healthcare professionals and specialists, including non-traditional customers and key decision makers.
• To understand customer insights around current standard of care and to support their knowledge of the value of our medicines to the NHS and patients.

Data generation and publication

• To acquire and maintain in-depth scientific knowledge of Pfizer medicines within nominated therapy area(s) (including those in development) as well as of key competitors.
• To deliver the medical plan in relation to medical projects, Investigator Sponsored Research (ISR) and support for Pfizer sponsored clinical research.
• To deliver other key medical and scientific activities within the medical plan, eg generation of real world evidence, non-interventional studies, database studies and registries (in collaboration with Access & Value colleagues) and ensure timely publication of data.

Support for clinical development

• To provide medical/scientific input into protocol feasibility assessments for clinical trial proposals.
• To identify appropriate investigators / sites for Pfizer-sponsored clinical trials.
• To work together with clinical research colleagues and in collaboration with above-country and global BU colleagues to drive the timely completion of Pfizer-sponsored clinical trials.
• To provide input into the regional and global clinical teams to ensure design and selection of trials relevant to UK needs, leveraging customer and patient insights.
• To support the effective implementation of approved compassionate use and named patient supply programs to ensure appropriate access to Pfizer medicines in response to HCP requests.

Data communication and customer insights

• To provide high-quality, accurate, balanced and specific information to customers in response to unsolicited requests for information.
• To provide scientific insight and support to field- and head office based commercial colleagues.
• To work with the cross functional team in-country and above-country to develop impactful and compliant promotional and non-promotional materials of value to customers.
• To review (and certify where applicable) promotional and non-promotional materials and activities within scope of the ABPI Code of Practice.
• To ensure customer intelligence is brought into the organisation to generate customer insights, shape future strategy and leverage business opportunities.
• To manage local advisory boards to gain customer insights.
• If media-trained, to present the scientific perspective on selected topics during media-briefings.

Cross functional medical and scientific support

• Support Access & Value in providing medical support for HTA dossiers and regional/local formularies.
• Support Regulatory Affairs in responding to questions from regulatory agencies and implementing changes to product SPC, PIL and PI. Provide support for clinical overviews, core datasheet revisions, license variations, batch specific variations and implementation of Risk Management Plans.
• Provide support to Medical Information to facilitate the maintenance of an accurate, relevant and high quality database which would enable them to respond effectively to customer enquiries.
• Provide scientific input to other departments (e.g. Government Affairs, Stakeholder Strategy, Communications, Customer Operations, Medical Quality and Compliance, Pfizer Research and Development groups) on a project-by-project basis.
• To provide specialist ABPI Code compliance support to brand/therapy area teams and other departments on customer engagement & partnership activities (e.g. Digital Programs, Joint Working, Medical & Educational Goods & Services, Advisory Boards).
• To develop and maintain ongoing cross-functional working relationships with Pfizer colleagues within the in-country, regional and global BU organisations.

QUALIFICATIONS

• Metabolic medicine / obesity experience required
• Medical Affairs experience
• Fluency in Business English
• Medical, Pharmacy or Science degree
• For medical applicants GMC registration with a License to Practice is preferred.
• For pharmacy applicants UK registration is preferred.
• For scientists a post graduate science degree (eg PhD, MSc) is preferred.

Organizational Relationships:
Reports to Medical Lead Internal Medicine

Resources Managed:
Project budget within medical plan

Work Location Assignment: Remote (within UK)

Equal Employment Opportunity: We believe that a diverse and inclusive workforce is crucial to building a successful business. Pfizer is committed to celebrating this in all its forms.