PharmaReview is an IQVIA business that provides outsourced medical copy review and approval services and advisory services to the pharmaceutical industry.
As a Final Medical Signatory, you will provide expert signatory services to our clients in line with the requirements of the PMCPA/ EFPIA code, MHRA Blue Guide
You will be working alongside PharmaReview Account Leads and Account Teams and Client Medical teams to deliver a seamless and consistent approach to certification. (The PharmaReview Account Teams are comprised of a group of reviewers that perform scientific, technical and quality checks of materials for scientific accuracy, quality and relevant pharmaceutical codes.)
This is a hybrid role requiring one day in the Paddington office / week.
Reports to
● Medical Director
Role and responsibilities
● Provide expert final signatory services to PharmaReview clients which include the certification of relevant items
● Act as an internal escalation point for signatory expertise in complex jobs
● Actively participate in and help lead internal Code training
● Maintaining up-to-date knowledge of Codes of practice (ABPI, IPHA, EFPIA, PhRMA) including any update and attending relevant training to either share or receive such updates.
● Act as the medical signatory representative for PharmaReview at client meetings as needed
● Active involvement in recruitment of reviewers and signatories as required.
● Coaching and mentoring of less experienced members of the team in technical and leadership skills
● Work with Compliance Team on internal and client audits as required
● Act as Code consultant to clients as required
● Track billable and non-billable work hours in time sheet
Key requirements for role
• Fluent in the English language
• UK registered pharmacist or registered physician
• Extensive knowledge of the applicable Codes of practice, including but not limited to the ABPI Code of Practice, EFPIA Code, IPHA Code, PhRMA Code, MHRA Blue guide
• Minimum 2 years' experience of Final signatory experience
• Minimum 5 years experience in Pharmaceutical Industry or equivalent
• Exceptional communication skills
• Collaborative and flexible approach
• Advanced critical appraisal skills and data interpretation
• Confident in decision making
Desirable
• Experience on an approval system like Veeva Promomats and/ or Aprimo
• Experienced in working in fast-paced environments.
Job Type
• Full time / Permanent Part time
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