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
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
