Medical Reviewer and Business Partner

4 weeks ago

Newcastle upon Tyne, United Kingdom TekWissen UK Full time

Role: Medical Reviewer and Business Partner

Duration: 6 months

37 hours per week

Location: Remote


ROLE RESPONSIBILITIES:

Provision of Code Expertise as a Medical Reviewer

• To review promotional and non-promotional materials and activities in line with the requirements of the ABPI Code of Practice.

• To review and sign-off materials as the Appropriately Qualified Professional (AQP) if named as a Pfizer AQP

Provision of Scientific Expertise in Relation to Content of Materials

• To acquire and maintain in-depth scientific knowledge of Pfizer medicines within nominated therapy area(s) (including those in development) as well as the competitive landscape.


Collaboration with Pfizer teams to Enable Streamlined Content Creation

• To work with the nominated cross functional team(s) in-country and above-country to develop impactful and compliant promotional and non-promotional materials of value to healthcare professionals and patients. This includes for example:

o advising on marketing programmes, other promotional activities and medical education

o providing support for revisions to prescribing information and implementation of risk management plans

o working with digital materials and digital technologies

o collaborating with Medical Affairs colleagues to understand therapy area and share pertinent issues with the relevant teams

• To provide specialist scientific and Code advice to teams during the development phase of materials/projects/activities to support streamlined creation of compliant content/activities that enable appropriate use of Pfizer medicines (where applicable) and successful implementation of materials, initiatives and programmes for example:

o advising on and reviewing materials for submission to health authorities eg prevetting submissions to the MHRA

o advising on and reviewing materials for package deals and materials for patient support (eg Homecare)

• To work in collaboration with cross-functional team(s) on preparation and review of training materials for colleagues

• To provide clear feedback and suitable recommendations to enable the above


Provision of support for above-country activities that fall within scope of the UK Code of Practice

• To collaborate and review, where required, global materials and activities, for example advisory boards, symposia, PAG donations, market research.

• To ensure relevant UK Medical Affairs teams are kept abreast of global initiatives in market


Thought Leader for Promotional Compliance Strategy

• To work in collaboration with the Code Approval Team and compliance leads to shape and evolve the promotional compliance strategy for Pfizer UK and to enable industry leading ways of working that are high quality, ethical and streamlined.


Support for Regulatory Labelling and Licence Maintenance Activities

• To support nominated cross-functional teams in the management of label updates (SPC, PIL, PI)

• To support nominated cross-functional teams in licence maintenance activities, including variations and renewals


Inclusive and time efficient working:

• To work collaboratively with team members and to agreed timelines.

• To effectively manage own time and workload.


Management of Complaints:

• When required, to work collaboratively on managing complaints or intercompany dialogue with internal and external stakeholders. Advise on corrective and preventative actions.


*Medical Reviewer and Business Partner - 1 x Rare Disease & 1 x Migraine

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