RESPONSIBILITIES:
- Creating clinical study protocols and reports, investigator’s brochures and regulatory submissions and ensuring consistency and compliance within the documents
- Act as a subject matter expert fielding queries from within the team and other internal stakeholders
- Analysing and interpreting data
- Supporting study projects, plans and statistical output
- Taking part in product development plans
- Assisting in in creating SOPs and related procedures
CANDIDATE:
- You will hold a PhD and strong relevant experience working within Biotech and Orphan Drugs
- Strong experience in writing and editing clinical regulatory documents
- Ability to analyse data and solve the conflicts
- Project management skills
- Working collaboratively
- Strong communication skills
Senior Medical Writing Scientist Recruitment Agency in London, Bio Technology Recruitment Agency in London