Med Info/Med Communications Executive IV Job in Cambridge, Anglia Uk
Our client based in Cambridge is looking for a Medical Information Executive/Medical Communications Executive to join their team on a 12 months contract. To be considered for this role, you will need to have 4 years Medical Information experience + copy approval and some experience of Medical Communications.
Responsible for:
Specific expert knowledge and data ownership of oncology products
Liaises with Medical Information to answer complex medical information enquiries
Planning and delivery of science-based product Medical Communication activities as a component of medical / brand teams based on local / regional strategies and team priorities
Compliance with regulations, processes and SOPs
Partnering and close cooperation with Medical Team and Brand Team members across functions, including Medical Information, other Scientific Affairs, Medical, and commercial functions
Ensuring close cooperation with MedCom headquarters and Scientific Publications
Review/Approval of non-promotional and promotional materials as per SOPs ABPI code of practice
Contributing to MedCom best practice development
Supports field based medical team and commercial team
Involved in training new starters on responsible products
Experience
•Scientific background (Candidates who have a BSc minimum with minimum 4 years experience in a medical information)
•Previous experience of copy Approval and the ABPI code of practice.
•Working knowledge of Oncology/has performed a similar role within a cancer setting.
•Cross collaborative working (Has to have worked with various people within medical i.e. Product Managers, Sales Representatives, Medical Team.
•The individual needs to provide evidence of presenting in front of a crowd (Confident in their knowledge and ability).
•Experienced within the industry, someone who has been involved from clinical through to authorisation.
•Prior experience with company correspondence relating to ABPI Code of Practice complaints.
•Experience of review and approval of training slides, Medical/Marketing Presentations.
•Preparation and consolidation of new clinical trial data into either new or re-approved standard letters
Key Words
•ABPI code compliance
•Product Launch
•Promotional
•Marketing support activities
•Proof-read, reference-check, signatory sign-off