At a Glance
- Tasks: Lead the creation of high-quality clinical documents for regulatory submissions.
- Company: Join Precision Medicine Group, a leader in innovative healthcare solutions.
- Benefits: Enjoy remote work flexibility, competitive salary, and professional growth opportunities.
- Other info: Collaborate with diverse teams and enhance your skills in a dynamic environment.
- Why this job: Make a significant impact in the healthcare field by ensuring quality in clinical documentation.
- Qualifications: Experience in medical writing and knowledge of regulatory guidelines required.
The predicted salary is between 50000 - 70000 £ per year.
Precision Medicine Group is seeking a Senior Medical Writer/Principal Medical Writer to lead the development of high-quality clinical study documents for regulatory submissions. The role includes planning, writing, editing, formatting, and QC review in line with ICH, FDA, GCP guidance and eCTD requirements.
The successful candidate will manage documents from template to final version, coordinate with Sponsor, external vendors, and internal Precision project teams, and translate complex clinical information.
Senior Medical Writer | Lead Clinical Documents (Remote UK) employer: Precision Medicine Group
At Precision Medicine Group, we pride ourselves on being an excellent employer by fostering a collaborative and innovative work culture that empowers our employees to make a real impact in the field of clinical research. With fully remote opportunities across the UK, we offer flexible working arrangements, comprehensive benefits, and continuous professional development to support your career growth. Join us to be part of a team that values your contributions and is dedicated to advancing healthcare outcomes.
