Regulatory Medical Writer

4,000 professionals, 0 days wasted, 1 incredible purpose. Together, we are beating cancer.
Regulatory Medical Writer - Centre for Drug Development
Salary: £36,000 - £44,000 pa + benefits
Contract type/ hours: Permanent/ full time 35 hours (flexible working requests considered)
Location: Stratford, London (High flex - we'd expect you to be in the office 1 or 2 days a week) or Home -based UK.
Application Deadline: Sunday 18th February at 23.55. This vacancy may close earlier if a high number of applications are received or once a suitable candidate is found, so please do not delay submitting your application to avoid any disappointment.
At Cancer Research UK, we exist to beat cancer
We are professionals with purpose, beating cancer every day. But we need to go much further and much faster. That's why we we're looking for someone talented, someone innovative and ambitious, someone like you.
What will I be doing?
This exciting role sits within the CRUK Centre for Drug Development, our goal is to bring much needed new treatments to people with cancer.
You'll be providing broad medical writing expertise for the production of clinical study reports, investigator brochures and other clinical/scientific reports for CDD's early phase oncology trials. Our Medical Writers have the opportunity to work across our broad portfolio of novel agents spanning antibodies, cell therapies, vaccines, drug conjugates and small molecules, making this an exciting and dynamic area to work in.
Key duties include:
Writing, editing, reviewing and quality control of documents for the timely production of clinical study reports and investigator brochures.
Managing the preparation of clinical study reports by building consensus with the project teams on report requirements, responsibilities for delivery of data and production timelines.
Managing the preparation and updating of investigator brochure packages in use in CDD‑sponsored trials, ensuring review at least annually in line with current regulations.
What skills are we looking for?
Proven experience in medical / medical sciences writing. This should include significant experience in Regulatory Medical writing or a mix of experience in Regulatory Medical writing plus substantial relevant experience in a related role in clinical trials, pharmacovigilance or medical writing.
Science graduate or equivalent experience of scientific writing.
Good knowledge of regulatory requirements for clinical trial documents e.g. investigator brochures, clinical study reports and posting of clinical trial summary results.
Excellent proofreading skills and attention to detail.
Confident communication skills and able to foster strong working relationships both internally and externally.
What will I gain?
Each and every one of our employees contributes to our progress and is supporting our work to beat cancer. We think that's impressive.
In return, we make sure you are supported by a generous benefits package, a wide range of career and personal development opportunities and high-quality tools, policies and processes to enable you to do your job well.
Our benefits package includes a substantial retirement plan, a generous and flexible leave allowance, discounts on anything from travel to technology, gym membership, and much more.
We review pay annually and aim to recognise individual performance and achievements.
We don't forget people have lives outside of work too and so we actively encourage a flexible working culture.
Our work - from funding cutting-edge research to developing public policy - will change the world. It's exciting to be part of our team.
How do I apply?
We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won't be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you quickly, fairly and objectively.
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