Medical Writer - Leeds, United Kingdom - Mednet Group

Mednet Group

Verified Company

Leeds, United Kingdom

2 weeks ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

About Mednet Group
Mednet Group is a group of award-winning healthcare communications agencies working with top 10 Global Pharmaceutical companies.

We have diversity and inclusion at our core and also lead the way as a partner of choice for socially conscious businesses.

About the role
In the context of its growth plan, Mednet Group is looking for a top talent as a Medical Writer.

The role involves writing compelling scientific and creative copy to support promotional and disease awareness campaigns. The medical writer role will also have an element of editing or broader communications.

Responsibilities include:

Distilling complex science into clear, engaging communications according to the client brief
Adapting your style to the audience and ensuring your messages are relevant and engaging
Making sure content meets the appropriate compliance codes and UK and EU regulations
Acting as an editorial consultant, showing ownership of data and the ability to source, write, reference, and adapt core claims with insight
Working to a high scientific and written standard showing great communication skills and building strong relationships that facilitate the production of great work

The position will be based at the Mednet Group headquarters in Leeds or with the option of working remotely. Reporting directly to the Head of Copy.

Be educated to degree level (2.1) qualification or equivalent
Have Masters or equivalent post graduate scientific qualification
Have experience working in a promotional healthcare communications agency across a broad range of therapy areas and products
Possess the ability to work within the constraints of the ABPI code of practice
Be able to manage your priorities as well as complex projects with a minimum of supervision demonstrating excellent organisational and project management skills
Have experience in using software and systems, including but not limited to:
Document management (version control processes, archiving)
Microsoft Suite (Excel/PowerPoint/Outlook)
Adobe Acrobat
Literature searching (including best practices and approaches) and other internet and intranet portals (e.g., SharePoint), resources, and search tools
Project review processes (iMR)
Possess great attention to detail and always be open to new ideas and ways of expressing them
Be familiar with diverse therapeutic areas, including the safety and efficacy profile of the compound(s) involved in the content and the associated disease state of interest
Biological sciences
Biopharmaceutics
Pharmacology (including pharmacokinetics and pharmacodynamics)
Drug development (e.g., phases of drug development) and clinical trial development (e.g., clinical trial design)
Scientific method, including hypothesis testing and clinical research methodologies
Statistics: accepted methods of data analysis (descriptive and inferential statistics) and techniques for communication of statistical results
Energetic and determined
Naturally enthusiastic
Selfmotivated
Committed to our values