Do you have experience writing and editing clinical regulatory documents?
Strong Leadership skills required.
This dynamic Pharmaceutical company is seeking an Associate Director with strong writing and editing skills in clinical regulatory documentation and experience managing a team and major projects. The Associate Director provides guidance and leadership for document development for regulatory filings and coordinates the clinical sections of more complex regulatory submissions, including organization, content, and resource requirements. You will need advanced technical expertise and develop solutions to complex problems, fostering interdisciplinary understanding and integrating the Medical Writing Departments activities within the organization.
To apply for this role, you need to have superior written communication skills and experience writing and editing clinical regulatory documents. In addition, you would need a broad understanding of drug development, clinical research, study designs, biostatistics, pharmacology, regulatory requirements, and medical terminology.
You need the ability to analyse, interpret and summarize complex and have the ability to manage project teams and multiple complex projects.
The ability to work in a creative, resourceful, self-sufficient manner and design alternative approaches to achieve desired results is essential.
The candidates need to have a related degree, Preferably to PhD level.
Salary: £90,000 - £100,000 Per annum / Bonus/Excellent Benefit package and Share offering