Medical Writer - Scientific Communications/HEOR manuscripts - Innovative Growing firm

JR United Kingdom; Leeds; Hybrid; GBP 30,000 - 50,000; Full time

Job summary

An innovative healthcare consulting firm in Leeds seeks a Medical Writer to draft, revise, and finalize scientific documents. This role offers the opportunity to work on global projects within a collaborative team, supporting career growth without sales pressure. Candidates should possess an MSc in a life science field and have strong writing experience in the pharmaceutical and public health sectors.

Qualifications

• 2+ years of experience in a technical writing role.
• Proven experience writing for the pharmaceutical industry and health economics.
• Strong clarity and accuracy in scientific communication.

Responsibilities

• Draft, revise, and finalize scientific materials.
• Collaborate with researchers to ensure scientific accuracy.
• Perform quality control reviews for documents.

Skills

Attention to detail

Interpersonal skills

Verbal communication

Education

MSc or other advanced degree in life science

Tools

Microsoft Office

Job description

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Medical Writer - Scientific Communications/HEOR manuscripts - Innovative Growing firm, Leeds, West Yorkshire

Client: Evidencia Scientific Search and Selection Limited

Location: Leeds, West Yorkshire, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views: 4

Posted: 31.05.2025

Expiry Date: 15.07.2025

Job Description:

New: Medical Writer (Remote UK/Hybrid possible) Innovative growing healthcare consulting firm

An exciting opportunity to join a growing consulting firm with one of the best staff retention rates in the healthcare/pharma space. Be part of a fun, people-focused culture where everyone looks out for each other, pulling in the same direction, finding a great balance between work and personal life.

The role would suit a medical writer who enjoys ‘hands-on’ writing, working in a collaborative, close-knit team. You will have an established leadership team to support your growth and development, with no pressure to be involved in sales/BD. The role provides good visibility in a mid-sized company and the chance to work on global projects.

Much of the company's work is repeat business and organic growth, with HEOR publications/manuscripts being a key deliverable. This new hire will contribute to these efforts.

Role scope:

• Draft, revise, and finalize scientific materials, including abstracts for scientific conferences, scientific posters, slide decks for podium presentations, tables, figures, and data visualizations.
• Articulate complex information clearly and concisely.
• Evaluate and interpret source documents, develop appropriate tables and figures.
• Provide copy editing, proofreading, and quality control reviews for other writers and researchers.
• Collaborate with internal researchers and client teams to ensure scientific accuracy using protocols, study reports, results tables, and other source documents to develop outlines and draft documents.
• Participate remotely in client-facing project meetings as needed.
• Incorporate author and reviewer comments to improve document accuracy and clarity.
• Address, revise, and clarify conflicting or ambiguous comments from authors and reviewers.
• Perform online searches of clinical literature and summarize findings.
• Coordinate and complete journal/abstract submissions adhering to guidelines and templates.
• Contribute to internal thought leadership projects.

Qualifications:

• MSc or other advanced degree in a life science, public health, or health economics-related field.
• 2+ years of experience in a technical writing role as a professional or student.
• Strong attention to detail, clarity, and scientific accuracy.
• Effective interpersonal and verbal communication skills.
• Proficiency in Microsoft Office (Word, PowerPoint, Excel).
• Proven experience writing for the pharmaceutical industry, public health, RWE, epidemiology, and/or HEOR is strongly preferred.