Analyst/Medical Writer

Dubizzle Limited; Cambridge, Manchester, Bristol, City of London; Hybrid; GBP 39,000; Full time

Job summary

A global healthcare agency in Cambridge seeks Analysts and Medical Writers to conduct detailed analysis of clinical trial data and create various materials. The role requires a scientific background, strong attention to detail, and excellent communication skills. Benefits include a starting salary of £39,000, hybrid working options, and comprehensive support for ongoing training and qualifications.

Benefits

Discretionary profit share bonuses

Hybrid and flexible working options

25 days’ annual leave plus bank holidays

Private medical insurance

Paid study leave

Qualifications

• An undergraduate degree in a scientific discipline (minimum 2.1 or equivalent).
• Experience planning and writing scientific documents and presentations.
• Strong analytical skills and attention to detail.
• Ability to manage multiple projects effectively.
• Fluency in Microsoft Word, Excel and PowerPoint.

Responsibilities

• Conducting detailed analysis of clinical trial data.
• Creating materials for different audiences.
• Supporting project management and client communication.
• Working on several projects across different disease areas.
• Participating in teleconferences and face-to-face meetings.

Skills

Detail oriented

Analytical skills

Project management

Effective communication

Proactive mindset

Microsoft Office Suite

Education

Undergraduate degree in a scientific discipline

Job description

Role Summary

• Responsibilities: You will work on projects that involve the detailed analysis and presentation of data from clinical trials, which are instrumental to the successful uptake of novel therapies
• Salary: £39,000 per annum (salary bands are determined by level of educational attainment to ensure a fair and consistent approach for all applicants, eliminating the need for individual negotiations)
• Benefits: Discretionary profit share bonuses paid twice per year, hybrid and flexible working options, generous holiday allowance, private medical insurance, critical illness cover, income protection, full funding for external training and more
• Role Type: Full-time, permanent
• Start Date: We are recruiting for start dates throughout 2026; you will state availability on your application form
• Application Deadlines: No set deadlines; role may close when suitable candidates are found
• Location: Global Headquarters in Cambridge, and offices in London, Manchester and Bristol

About the Role

Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical trials and the assimilation and creative presentation of this analysis in different formats. Deliverables include posters, slide sets, value dossiers, reports and peer-reviewed publications used by clients in communications with external stakeholders, supporting the uptake of novel therapies. Work is project-based, typically across several disease areas.

You will work in project teams alongside experienced colleagues who provide one-to-one training in project management and client communication. Delivering project work requires close collaboration with clients, and you will participate in teleconferences and face-to-face meetings with external stakeholders.

Costello Medical is structured into teams focusing on medical communications, health economics services, or specific healthcare sectors. You may specify team interests in your application; you will be assigned a home team but will work across teams where possible to develop a broad understanding of services and clients.

Market Access, HTA, Medical Affairs, Literature Reviews, Publications, Rare Diseases, MedTech, Real-World Evidence, Pro Bono, Health Policy, Health Economics and Statistics are key service areas. A role in these teams involves evidence generation, literature reviews, stakeholder engagement, economic modelling, and creating global materials to demonstrate value and support patient access. The roles suit those with an interest in patient access to healthcare, fast learning, strategic thinking and strong writing skills.

Key responsibilities include:

• Conducting detailed analysis of clinical trial data and creating materials for different audiences
• Participating in teleconferences and meetings with external stakeholders
• Supporting project management and client communication
• Working on several projects in different disease areas
• Engaging with different teams to develop understanding of service offerings and clients

Hybrid Working Policy: We offer flexible arrangements with up to half time remote work after probation; during the probation period, up to 1 day per week from home.

A Day in the Life of an Analyst or Medical Writer

For more about a typical day, please see the company information provided in the application materials.

About Costello Medical

Costello Medical is a global healthcare agency specialising in medical communications, market access and health economic outcomes research. We work with a range of clients in the pharmaceutical and medical device sectors. We have been recognised in various industry lists and accreditation programs. More information is available on our website.

About You

The following essential requirements apply:

• An undergraduate degree in a scientific discipline (minimum 2.1 or equivalent); postgraduate qualifications are advantageous but not required. Applications from diverse specialisms are welcome
• Experience planning and writing scientific documents and presentations
• A self-motivated, enthusiastic approach and genuine interest in healthcare
• Attention to detail and strong analytical skills
• Excellent organisational skills and the ability to manage multiple projects
• Exceptional written English and effective verbal communication
• Ability to tailor communication to a variety of audiences
• Proactive mindset and collaborative team approach
• Willingness to contribute to the wider team and embody Costello Medical values
• Fluency in Microsoft Word, Excel and PowerPoint

Joining Costello Medical from Academia

We welcome applicants from academia transitioning into industry, with training, mentorship, and a collaborative culture to support the transition.

What We Offer

We offer a comprehensive benefits package including:

• Starting salary of £39,000 and discretionary profit share bonuses
• 25 days’ annual leave plus bank/public holidays, plus holiday buy/sell scheme
• Flexible working hours and up to half-time remote work after probation
• Flexible benefits, private medical insurance, paid study leave and funding for external qualifications
• Critical illness cover, income protection and life assurance
• Paid and unpaid sabbaticals based on length of service

The Application Process

Submit your CV and a cover letter via our online form. Your cover letter should explain why you are suited to the role with examples; include dates of qualifications. Your CV should clearly state qualification dates and grades.

Our recruitment process includes proofreading and a written assessment, followed by interviews and a short presentation.

We are an equal opportunity employer and offer reasonable adjustments during recruitment. More information is available on our site.

Note: Some roles may involve confidential data; please do not rely solely on AI to generate application materials.

Visa Sponsorship

Visa sponsorship eligibility is limited to New Entrants (under 26, currently studying in the UK or a recent UK graduate), PhD holders in STEM or in a role-relevant field.

You will be asked to provide right-to-work details in your application. See UK government guidance for more information.

Student to Graduate Visa

Current Student visa holders may need to submit a graduate visa application before joining in a permanent full-time role. For details, consult GOV.UK guidance. For questions, contact [e-mail].