Senior Medical Writer/Principal Medical Writer
Precision Medicine Group · Remote, United Kingdom
Posted about 3 months ago
or apply directly on Precision Medicine Group's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 80 days Precision Medicine Group's roles stay open a median of 81 days
- Reposted
- No
- Salary listed
- No 0% of Precision Medicine Group's roles list one
- Ghost-job risk at Precision Medicine Group
- high 152 stale, 8 reposted of 157 open
- Hiring momentum
- 309 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-10-23
Measured from postings appearing on and disappearing from Precision Medicine Group's own greenhouse board since 2026-08-03. Full hiring picture for Precision Medicine Group.
About this role
The Senior Medical Writer/Principal Medical Writer will lead the creation of clinical study documents, ensuring they meet regulatory guidelines and are completed on time. Responsibilities include planning, writing, editing, and reviewing documents such as clinical study protocols and clinical study reports, while collaborating with various teams and maintaining high standards of quality and compliance.
- benefits
- 1/5
- freshness
- 1/5
- career value
- 4/5
- role clarity
- 4/5
- pay transparency
- 0/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Precision Medicine Group as an employer.
What you need
- BS degree or equivalent in a scientific or medical discipline with relevant writing expertise
- 5+ years of experience as a Sr. Medical Writer in the sponsor and/or CRO setting or 7+ years of experience as a Principal Medical Writer
- Proficiency with Microsoft Windows, Teams, Word, Excel, Adobe Acrobat, and PowerPoint
- Clear understanding of applicable regulations (eg, ICH, FDA, GCP), clinical trial transparency requirements (ie, EudraCT, CT.gov), and eCTD requirements for all phases of development
- Impeccable attention to detail and ability to complete writing assignments in a timely manner
- Ability to work effectively in a fast-paced environment with multiple high-priority projects with no instruction on routine work and minimal instruction on new assignments
Nice to have
- Advanced degree (MS/PhD)
- Oncology and/or rare disease experience (especially protocol and CSR development)
Worth weighing
- Remote position may require self-discipline and effective communication in a virtual environment
- No specific salary or benefits mentioned in the posting
- Requires a strong understanding of regulatory guidelines, which may be challenging for those without prior experience in clinical writing
Summarised from Precision Medicine Group's posting. Read the full original.
Listed by Precision Medicine Group on their greenhouse job board, last confirmed open on 2026-10-23. PitchMeAI is not the employer.
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