Be at the heart of actionFly remote-controlled drones into enemy territory to gather vital information.

Apply Now

Scientific Writer

Russell Tobin
London
7 months ago
Applications closed

Related Jobs

View all jobs

Senior Medical Writer

Regional Sales Manager

Scientific Customer Support Coordinator

Scientific Lead

Technical Sales Executive

Associate Principal Scientist R&D

Expert Scientific Writer

PAY 400 Pounds Per day/6 month contract/Hybrid


Job Purpose

  • To manage and complete assigned Medical Communications deliverables at high quality standards and in accordance with agreed timelines.
  • Projects include manuscripts, abstracts, posters, slide sets, satellite symposia content, congress or advisory board reports, publication planning and medical education materials for internal medical and/or clinical teams.


Major Activities

1. Demonstrate a command of assigned therapeutic areas and expertise with assigned products.

2. Research and write original content for publications activities (primary and secondary manu-scripts, review articles, abstracts, posters), slide presentations and other materials based on direction and materials supplied by customers.

3. Prepare meeting materials for satellite symposia (agenda, slide content, speaker briefings etc.), and reports from advisory boards and other internal or external meetings.

4. Develop content that is scientifically accurate, evidence-based, grammatically accurate, referenced using appropriate sources, and consistent with quality standards for author review, customer review as appropriate, and scientific peer review.

5. As needed, perform quality control (QC) checking / proof reading of the above-mentioned documents to meet customer expectations.

6. Clearly communicate medical scientific concepts in a condensed, audience-appropriate way.

7. Follow all internal processes and procedures with regard to workflow, development of deliverables, and adherence to industry best practices, including GPP3.

8. Demonstrate the flexibility/adaptability necessary to function on different therapeutic teams as needed and to work on projects across multiple brands at any given time.

9. Interpret and apply clinical data in medical communication deliverables.

10. Work in conjunction with service team and line manager to develop and adhere to logical and attainable timelines for project completion.

11. Provide input and aid in troubleshooting/problem-solving.

12. Collate and incorporate author/customers comments.

13. Lead and/or participate in author/client teleconferences.

14. Provide accurate citations in text (utilizing Reference Manager system), a bibliography, and appropriately annotated references for medical review.

15. Participate in strategic and tactical publications planning and related research.

16. Work as part of a team; mentor new and less experienced colleagues as and when required.

17. Support people and performance management.

18. Maintain records for all assigned projects including archiving.

19. Maintain audit, SOP, WP, and training compliance.

20. Perform additional work-related tasks as assigned. Travel may be required


Key Performance Indicators

1. Adheres to quality, timeliness, and productivity of deliverables as per KPI targets.

2. Attention to detail and high degree of scientific and medical accuracy in medical writing.

3. Ability to identify key issues and to overcome challenges or obstacles creatively and strategi-cally.

4. Sound analytical thinking, planning, prioritization, and execution skills.

5. Well-developed professional communication skills, including written and inter-personal.

6. Exceptional organizational skills with adeptness at multitasking.

7. Flexibility and adaptability to change; ability to work under time constraints.

8. Ability to interact effectively in a team-oriented environment.

9. Established track record of high-quality medical communications outputs (e.g., manuscripts, posters, etc.).

10. Understanding of good publication practice guidelines (GPP3).

11. Adheres to Novartis values and behaviors.


Ideal Background

Education:

  • Minimum: Minimum science degree or equivalent.
  • Desirable: MSc, PhD, PharmD, or MD


Experience

  • Minimum of 5 years’ experience in medical communications.
  • Medical writing experience.
  • Good understanding of industry work processes for publications.
  • Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook).

Subscribe to Future Tech Insights for the latest jobs & insights, direct to your inbox.

By subscribing, you agree to our privacy policy and terms of service.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Biotechnology Recruitment Trends 2025 (UK): What Job Seekers Must Know About Today’s Hiring Process

Summary: UK biotechnology hiring has shifted from title-led CV screens to capability-driven assessments that emphasise validated lab results, documentation, GxP/QA/RA awareness, data literacy, digital biology tools & measurable impact from bench to bedside. This guide explains what’s changed, what to expect in interviews & how to prepare—especially for wet-lab scientists, bioprocess/CMC engineers, QC/QA specialists, RA/clinical professionals, bioinformatics/data scientists & platform engineers. Who this is for: Biologists, biochemists, biotechnologists, cell & gene therapy scientists, upstream/downstream processing engineers, QA/QC analysts, validation engineers, regulatory affairs specialists, clinical trial professionals, bioinformaticians, data scientists & biotech product/operations managers targeting roles in the UK.

Why Biotechnology Careers in the UK Are Becoming More Multidisciplinary

Biotechnology once meant pipettes, lab benches & research reports. But in today’s UK job market, biotech careers are no longer confined to wet labs or sequencing centres. As the sector expands into gene therapies, synthetic biology, personalised medicine, agricultural biotech, and bioinformatics, professionals are expected to integrate not just biology & chemistry, but also law, ethics, psychology, linguistics & design. This change reflects a broader truth: biotechnology doesn’t happen in isolation. It impacts people’s health, the environment, food supply & society at large. That means careers in biotech now require more than scientific knowledge — they demand legal awareness, ethical reasoning, patient empathy, clear communication, and user-centred design. In this article, we’ll explore why biotech careers in the UK are becoming multidisciplinary, how law, ethics, psychology, linguistics & design are shaping job descriptions, and what job-seekers & employers need to do to succeed in this transformed landscape.

Biotechnology Team Structures Explained: Who Does What in a Modern Biotechnology Department

Biotechnology is a fast-moving, highly interdisciplinary sector that spans research, development, clinical trials, manufacturing, regulatory affairs, and commercialisation. In the UK, biotech firms, pharmaceutical companies, academic spin-outs, and contract research organisations (CROs) are collaborating more than ever, leading to the creation of complex teams with specialised roles. To deliver safe, effective, and compliant biotech products — whether diagnostics, biologics, gene therapies, environmental biotech, or agricultural innovations — it's vital to know who does what. This article will map out the structure of a modern biotech department. We’ll define the key roles, how they interact across the product lifecycle, what skills are required in the UK, typical career paths, salary expectations, and examples of how startups versus large firms organise themselves. Whether you are a hiring manager or a job seeker, this will help you understand the landscape of biotechnology jobs in the UK.