Senior Regulatory Medical Writer (CTD) UK
United Kingdom – Home based
Are you looking for your next career move which also allows you to have a work life-balance? I am looking for an experienced Regulatory Medical Writer to join a market leading and prestigious consultancy. This opportunity will allow you to deal with international clients after completing an extensive training program. In this role you will also be able to contribute to the success of the company by having your opinion heard.
The service you will provide is more than just writing, you will be an essential part of the clinical development teams across different therapeutic areas.
Your experience as a Senior Regulatory Medical Writer
At least 3 years of experience actively writing Clinical Summaries in CTD format
You also have experience writing the following: Clinical Study Reports / Protocols, Investigator Brochures, scientific publications
Experience interacting directly with clients or authors of the documents and coordinating review cycles, meetings, and project timelines
In order to apply successfully you will also need to have:
Diploma/Masters/Bachelor’s degree in science/pharmacy
Fluent written and spoken English skills
An eye for details and flexibility
Excellent, proven interpersonal skills and enjoy proactively participating on a team with diverse personalities
Should you be interested in this opportunity then do not hesitate to send your CV to Adrienn Nora Kovacs -firstname.lastname@example.org. You can also call +49 69 2740 15840 for more information.