Regulatory Affairs Copy Review Specialist

3 days left

Up to £2250 per month
15 Feb 2021
01 Mar 2021
Dominic Bellenger
Regulatory Affairs
Full Time
Contract Type
Experience Level
Experienced (non-manager)
Regulatory Affairs Copy Review Specialist

My client, a leading medical devices company is looking for a Regulatory Affairs Copy Review Specialist to join their team based in the UK. Experience in copy review and a strong understanding the ABHI code of conduct required.

Overall purpose of job:

Drawing on relevant expertise and information from both internal and external sources, responsible for the review and approval of promotional and advertising assets and professional education resources for hospital Medical Devices.

Essential duties and responsibilities:

· Supporting all business across the HMD group of companies in reviewing and approving copy review of assets

· Setting and communicating timelines for approvals with commercial partners.

· Working to strict deadlines provided by the commercial partners.

· To work with other members of the team to increase knowledge on products.

· Reviewing company practices and providing advice on changes to systems.

Job Requirements

Essential knowledge and skills:

Successful graduation in a Life Science degree or equivalent

· Proven copy review experience in medical devices

· Proven knowledge of the ABHI Code of Conduct

· High degree of initiative

· Team player, fosters the strength of a network

· Well organised, sense for detail

· Able to cope with fluctuating and high work-load demands

· Fluent in English

Core competencies required for this role:

· Strong team player

· Excellent communication and interpersonal skills, ability to influence and motivate

· Proven success at meeting strategic goals and KPIs

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All questions are required

Do you have an understanding of the ABHI code of conduct?

Do you have experience in Copy Review of Medical Devices?

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