Regulatory Medical Writer
Apply locations: Stratford (2 Redman Place), Home Based - Northern Ireland, Home Based - Wales, Home Based - Scotland, Home Based - England
Time Type: Full time
Posted On: Posted Yesterday
Time Left to Apply: End Date: December 9, 2024 (9 days left to apply)
Job Requisition ID: R030017
Salary: £36,000 - £44,000 plus benefits
Reports to: Medical Writing Manager
Directorate: Research & Innovation
Contract: Permanent
Hours: Full time 35 hours per week (flexible working requests considered, minimum 32 hours per week)
Location: Homebased or Stratford, London (1-2 days a week in the office)
Closing Date: 08 December 2024 23:55
This vacancy may close earlier if a high volume of applications is received or once a suitable candidate is found; therefore, we strongly recommend that you apply early to avoid disappointment.
Visa Sponsorship: You must be eligible to work in the UK to apply for this vacancy. Cancer Research UK is not able to offer visa sponsorship.
Recruitment Process: Pre-prepared task followed by competency-based interview
Interview Date: W/C 13 Jan 2025 (Shortlisting will take place in December)
At Cancer Research UK, we exist to beat cancer.
Cancer Research UK is looking for a Regulatory Medical Writer. This role sits within the CRUK Centre for Drug Development, where our goal is to bring much-needed new treatments to people with cancer.
As a Medical Writer, you’ll provide 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. You will act as lead author on your assigned projects and perform quality control review of documents produced by other Medical Writers, fully embedded within a multidisciplinary, cross-functional project team.
What will I be doing?
1. Writing, editing, reviewing, and quality control of documents for the timely production of clinical study reports and investigator brochures.
2. Managing the preparation of clinical study reports by building consensus with project teams on report requirements and timelines.
3. Managing the scheduling, preparation, and updating of investigator brochure packages.
4. Liaising with the project team to complete project-specific tasks including review of protocols and Trial Master Files.
What are you looking for?
1. Proven experience in medical/medical sciences writing.
2. Science graduate or equivalent experience of scientific writing.
3. Good knowledge of regulatory requirements for clinical trial documents.
4. Excellent proofreading skills and attention to detail.
5. Confident communication skills and able to foster strong working relationships.
6. Project Management skills.
7. Experience within early phase oncology trials is desirable but not essential.
We’re looking for people who can embody our organisational values: Bold, Credible, Human, and Together. If you’re interested in applying but are unsure if you have the right skills and experience, we’d still love to hear from you.
What will I gain?
We create a working environment that supports your wellbeing and provide a generous benefits package, career development opportunities, and high-quality tools.
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.
About Us
As the world’s largest independent cancer research charity, we conduct research into the prevention, diagnosis, and treatment of the disease. Our aim is to see 3 in 4 people survive cancer by 2034.
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