Knowledge of the drug development process and understanding of the basic strategy for regulatory submissions is an asset. Experience in writing for regulatory submissions to the European or US regulatory authorities is required (e.g., CTD modules, ISS, ISE, scientific advice/briefing documents). The ideal candidate will have a PhD in a biological sciences discipline and 3 to 4 years’ regulatory writing experience in medical/regulatory/publication writing in the pharmaceutical/biotech industry, CRO, or medical communications agency. The position can be either based at home in the UK or at our offices in Manchester city centre.

We are seeking a Senior Regulatory Writer to join our team. You will already have successfully led typical editorial projects from start to finish, delivering to time and budget and managing the expectations of clients and healthcare professionals.Īs well as providing a competitive salary and benefits package, Meridian HealthComms offers an ethos of scientific excellence coupled with a collegiate and supportive environment. You will have a proven track record as a Senior Writer or Principal Medical Writer in a medical communications agency. You are likely to be actively seeking your next career step. The Scientific Director will be a member of the Meridian management team and will actively participate in and contribute to management meetings and the subsequent discussions and decisions that affect the day-to-day management, direction and success of the entire business. The ideal candidate will have a PhD in a biological sciences discipline or life science.

The purpose of the role is to provide scientific expertise and guidance to the business and clients. The position can be either based at home in the UK or at our offices in Manchester city centre.

Meridian healthcare