Analyst/Medical Writer

Responsibilities and Compensation

• 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 (we have established salary bands determined by your 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 currently recruiting for start dates throughout 2026, and you will be asked to state your availability on your application form.
• Application Deadlines: Whilst there are no set application deadlines, we strongly recommend applying as early as possible. The role, or particular start dates, may close when suitable candidates are found.
• Location: This role is available in our Global Headquarters in Cambridge, as well as our London, Manchester and Bristol offices.

Role Summary

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. These deliverables include posters, slide sets, value dossiers, reports and peer‑reviewed publications, and they are used directly by our clients in communication with a range of external stakeholders, making them instrumental to the successful uptake of novel therapies. The work is structured on a project‑by‑project basis and you will usually be working on several projects in different disease areas at any one time.

About the Role

You will work in project teams alongside experienced colleagues, who provide one‑to‑one training in the technical aspects of the role, including project management and effective client communication. Delivering project work requires close collaboration with clients, and following a successful induction period you will increasingly participate in teleconferences and face‑to‑face meetings with external stakeholders.

Market Access

Within the healthcare sector, the Market Access process is essential to ensuring that medicines are reimbursed and rapidly made available to patients who need them. Our Market Access team supports a wide range of clients in developing the communication strategy essential to demonstrating the clinical and economic value of some of the newest, most innovative therapies in development. Our work is multidisciplinary, often beginning with evidence generation in the form of literature reviews, advisory boards with clinicians and payers, or economic modelling, to inform the development of global materials that present an evidence‑based account of the product\’s value in a compelling and accessible manner. These materials are used by our clients for the creation of further regional materials, ensuring that the product communication strategy is consistent across local market\’s pricing and reimbursement submissions. As a result, our work has a direct impact on patient access to medicines worldwide. We also create local materials, from reports to help our clients understand the marketplace that their products will be entering, through to leave‑pieces to educate payers about the budget and resource implications of new, high‑impact medicines coming to market. A role in the Market Access team suits those who are passionate about patient access to healthcare and are fast‑learners, with a strategic, problem solving mindset coupled with exceptional writing skills.

HTA

By joining the Health Technology Assessment (HTA) team you will work on the successful delivery of projects to demonstrate the clinical and health economic value of some of the newest and most innovative therapies in development. In countries where HTA represents the final hurdle before a new therapy can achieve patient access, your work will have a direct impact on the successful reimbursement of these therapies. You will work closely with your clients to develop the HTA strategy for each project from the outset and will use your excellent written communication skills and scientific understanding to create clear, evidence‑based, and strategic narratives to help demonstrate the cost‑effectiveness of new therapies to the healthcare system. To date, the HTA team at Costello Medical have worked on over 100 submissions to national reimbursement agencies, including the National Institute for Health and Care Excellence (NICE) in the UK, the European HTA agency EUnetHTA and Singapore\’s Agency for Care Effectiveness (ACE). No prior experience or knowledge of economics is required (though there is considerable opportunity to develop knowledge of health economics in the role), but good numerical skills, the ability to critically appraise clinical evidence and strategic thinking are key to the role.

Medical Affairs

Medical Affairs provides the scientific bridge between clinical development and commercial functions in pharmaceutical and device companies. Most activities have a strong patient and/or healthcare professional (HCP) focus, and act to educate and inform clinical decision making and patient care, or to gather insights that inform a product\’s clinical development. As a member of the Medical Affairs team, you will work closely with our clients to present the ‘science behind the product\’ through a wide range of projects including medical education events, advisory boards and medical information materials. You will collaborate with and support expert advisors and event speakers, and the requirement for on‑site support at certain events provides opportunities for international travel. You will develop a complementary set of strong scientific, creative and writing skills, as well as the opportunity to become extremely knowledgeable about the therapy areas in which you work. The ability to creatively present scientific information to a wide range of audiences would be valuable in this role.

Literature Reviews

Literature Reviews projects involve the identification of clinical, economic and real‑world evidence to support the value of a pharmaceutical product or medical device. Our work includes rigorous systematic literature reviews that can be used to inform meta‑analyses and network meta‑analyses, as well as more creative and pragmatic evidence reviews to inform clients\’ strategic decisions with regard to clinical development or market access. You will gain a thorough understanding of how to conduct various kinds of evidence review from searching to interpretation of results, ensuring that the reviews conform to industry guidelines where applicable. You will also be involved in writing up the methods and results of the reviews into engaging reports and slide sets. Furthermore, as original research in their own right, we publish many of our reviews as conference presentations or journal publications. This role suits those who are passionate about the concept of evidence‑based medicine, have excellent attention‑to‑detail and organisational skills, and a talent for communication.

Publications

As a member of the Publications team you will work closely with clients and world‑renowned opinion leaders to produce publications that communicate key scientific and clinical data to a wide audience. This includes the development of abstracts and manuscripts, as well as posters and oral presentations for large international congresses, with the opportunity to provide on‑site support at such events. In addition, you may have the chance to work on regulatory documents, plain language summaries and policy‑related publications. You will receive one‑to‑one training on the technical aspects of the role, including good publication practice and strategic publication planning. This role is for those looking to apply their scientific writing and creative skills to deliver high‑impact publication projects to a wide range of clients.

Rare Diseases

To date, over seven thousand rare diseases have been identified but only four hundred have an approved treatment; our specialised Rare Diseases team supports this sector in overcoming the unique challenges they face, such as an urgent need to bring treatments to patients, little clinical or health economic evidence and limited understanding of the condition across the clinical community and society as a whole. By joining this team, you will develop the appropriate skills and deliver projects that require a broad range of technical expertise and knowledge across all of our service offerings, including literature reviews, the development of global economic models and publications, and the organisation of medical education events. You will also have the opportunity to work on some of the most cutting‑edge treatments, such as gene therapies, supporting patients in accessing potentially life‑changing treatments. This is an exciting time to join our growing Rare Diseases team and to apply your exceptional written and technical skills to the rare diseases field, leading to a measurable impact on access to novel, often life‑extending, treatments for rare disease patients.

MedTech

Manufacturers of medical devices face different challenges to pharmaceutical companies, and therefore we have a dedicated team that supports this distinct sector of the healthcare industry. Our MedTech team helps medical device manufacturers in bringing new technologies to market, and communicating the value of their brand. By joining this team, you will gain an understanding of the delivery of all our service offerings, with a focus on conducting literature reviews, compiling evidence summaries, creating key value messages and developing evidence‑based customer‑facing materials (such as brochures, apps and health economic tools). You will work in a growing team and develop strong relationships with clients, being able to support them through all aspects of their work. You will also help refine newer services for the team and attract new clients. A strong interest in medical devices is essential for the role, along with a flexible nature to accommodate the various needs of clients, and the ability to compellingly communicate the value of a product to a wide range of audiences.

Real‑World Evidence

Real‑world evidence (RWE) is becoming increasingly important for the demonstration of clinical and economic value of pharmaceuticals and medical technologies. Our RWE team contribute to the design, execution and subsequent reporting of prospective, retrospective or cross‑sectional real‑world studies. They develop protocols and statistical analysis plans (in collaboration with our Statisticians, clients and external experts), acquire and analyse data, and communicate the methodologies and results in both written and oral formats. Studies include data from patient registries, claims databases, prospective studies or any other source of real‑world data, and involve a wide range of research questions on burden of disease, clinical effectiveness or economic topics, among others. As one of our most recently established teams, this is an exciting time to join our growing RWE team; you will play a key role in shaping the future of Costello Medical\’s RWE service offering by delivering high‑quality real‑world studies that can make a meaningful impact in a wide range of disease areas. The role would be well‑suited to someone with an interest in epidemiology or biostatistics, although no formal background in these areas is required.

Pro Bono

Our Pro Bono team delivers projects free‑of‑charge to charities and not‑for‑profit organisations within the pharmaceutical and medical device sectors, with the aim of making a real difference to causes that our staff care about. We offer our full range of services on a pro‑bono basis, working collaboratively across our teams and office locations to secure the right expertise to fulfil project briefs. By joining as an Analyst within our Pro Bono team, you will develop the appropriate skills and deliver projects that require a broad range of technical expertise and knowledge across our service offerings, including health economics, literature reviews, medical writing, peer‑reviewed publications, medical education and design materials.

Health Policy

Communications play a central role in health policy, helping to inform policy change at both the local and global level. At Costello Medical, our team provide end‑to‑end support on a diverse range of health policy projects to address unmet needs, promote best practice and, ultimately, enhance the quality of care for patients. We combine a strong scientific understanding, passion for health policy, ability to tailor language to different target audiences, and in‑house design skills to develop impactful health policy publications.

Health Economics

You will work on projects involving the development of economic models, as well as the communication of the relevant methods and results to clients in a variety of formats, such as reports and slide decks. Health economics projects involve developing economic models that determine whether interventions are good value for money and/or provide an affordable treatment option to the healthcare system. You will support the Health Economists who analyse the data, which could involve writing up protocols and reports or searching and validating model inputs.

Statistics

You will work on projects involving the statistical analysis of data, as well as the communication of the relevant methods and results to clients in a variety of formats, such as reports and slide decks. Statistics projects involve analysing patient‑level clinical trial data, observational study data, real‑world data and published aggregate data to answer particular questions about relevant treatments; for example, whether one treatment is more effective than another in terms of a given outcome. You will support the Statisticians who analyse the data, which could involve writing up protocols and reports, searching and validating model inputs and providing input to the validity of model structures or assumptions used in statistical analysis from a clinical or scientific perspective.

Key Responsibilities

• Conducting detailed analysis of clinical trial data and creating materials for different audiences in various formats.
• Close collaboration with clients, including participating in teleconferences and face‑to‑face meetings with external stakeholders.
• Supporting project management and client communication, alongside experienced colleagues.
• Working on several projects in different disease areas at any one time.
• Engaging with different teams within the company to develop a broad understanding of service offerings and clients.

Hybrid Working Policy

We believe that having face‑to‑face time in the office holds many benefits and is central to ensuring that the community we have created, where people have a workplace they belong to and feel part of, is never lost. At the same time, we recognise that homeworking can improve work life balance, reduce commuting times and costs, and provide the opportunity to juggle personal commitments. Therefore, we offer flexible working arrangements that allow our colleagues who have passed probation to work from home for up to half of the time, measured across a 2‑week rolling period. During your probationary period (normally the first 6 months of the role), you will be able to work from home for 1 day per week.

A Day in the Life of an Analyst or Medical Writer

To learn more about a typical day for an Analyst or Medical Writer at Costello Medical, please click here: Working At Costello Medical | Costello Medical.

About Costello Medical

Costello Medical is a rapidly growing global healthcare agency specialising in medical communications, market access and health economic and outcomes research. We work with a wide range of clients, including the industry\’s most successful pharmaceutical and medical technology companies, patient and public health bodies and charitable organisations. We have been listed on the Top 100 Best Companies to Work For list since 2017, as well as receiving B Corporation Accreditation in 2022. Please click here to learn more about us, our work and our mission: https://www.costellomedical.com/.

Requirements

About You

In addition to the specific scientific skills and experience you need to succeed in your role, we have developed a framework that details the key skills, approaches and mindsets that are essential for all Analysts and Medical Writers to display in order to excel in their role with us. Embodying these will support your growth and development throughout your career at Costello Medical.

Essential Requirements for the Role

• An undergraduate degree level qualification in a scientific discipline (minimum 2.1 or equivalent). Postgraduate qualifications (minimum 2.1 or equivalent) would be an advantage, but they are not a requirement for the role. We welcome applications from candidates with a diverse range of specialisms, including but not limited to biology, chemistry, pharmacy and medicine.
• An aptitude for, and experience of, planning and writing scientific documents, which could include lab reports, dissertations, poster or oral presentations, articles for websites or student magazines, peer‑reviewed scientific publications, book chapters, grant applications, and regulatory documents.
• A self‑motivated and enthusiastic approach, with a genuine interest in healthcare and an eagerness to learn and develop your skills.
• An exceptional level of attention to detail.
• Strong analytical skills.
• Excellent organisational skills, with the ability to manage your time to work across multiple projects at the same time and prioritise tasks appropriately to maximise productivity.
• Exceptional written English, which you will use in client work, email communication and internal messaging.
• Effective verbal communication skills, which you will use when working with colleagues and clients.
• The ability to tailor your communication style to a variety of audiences, including healthcare professionals, patient groups, suppliers, clients, non‑scientific colleagues and governmental bodies.
• A proactive mindset, including the ability to recognise challenges and suggest solutions with limited guidance.
• A collaborative approach to working, where you share knowledge with others in your team to promote the attainment of a common objective, and work together to overcome obstacles to success.
• The self‑awareness to reflect on your own work and performance, alongside a willingness to take ownership of your work and the development of your career.
• A willingness to get involved with, and contribute to, your wider team.
• Embodying Costello Medical\’s values, which includes being committed to delivering quality work, championing innovation in healthcare, acting with integrity and supporting your colleagues as they would support you.
• Fluency in Microsoft Word, Excel and PowerPoint.

Joining Costello Medical from Academia

At Costello Medical, we warmly welcome applicants from academia who are looking to transition into a role within a commercial, industry‑based setting. We understand the unique perspectives and valuable skills that academic professionals bring to our team. To support your career change, we offer comprehensive training, mentorship programs, and a work culture that fosters collaboration, growth and innovation. We are committed to facilitating a smooth transition and helping you thrive in an industry‑based setting.

Benefits

What We Offer

• A starting salary of £39,000 per annum, as well as a discretionary profit share bonus paid twice per year. Please note that we have established salary bands that ensures a fair and consistent approach for all applicants, eliminating the need for individual negotiations.
• 25 days\’ annual leave plus bank and public holidays, as well as a holiday buy and sell scheme.
• Flexible working hours and the chance to work from home for up to half of your working time after passing probation.
• Flexible benefits scheme offering cash payments, additional pension contributions and more.
• Private Medical Insurance which offers comprehensive cover on a \”medical history disregard\” basis.
• 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

You are required to submit your CV and a cover letter via our online application form. In your cover letter, you must explain why you think you would be suited to the role and why you would like to join Costello Medical, with examples to support both. Your CV should clearly state the dates of all qualifications and grades achieved where applicable.

Then, our recruitment process includes a proofreading and written assessment for you to complete in your own time. If successful, you will be invited to an interview which will include a short presentation you can prepare for in advance.

As an equal opportunity employer, we are committed to fostering a diverse and inclusive workforce and, throughout the recruitment process, there are a number of reasonable adjustments we can provide. Please click here to learn more.

Please note that, whilst we embrace AI to innovate and improve processes, your role may involve confidential data that cannot be uploaded to AI. Therefore, it is important for us to assess your own skills and abilities, so we recommend that you do not rely solely on this technology to generate any application materials.

Visa Sponsorship

• Due to the Skilled Worker visa regulations, you will only be eligible for visa sponsorship if you meet at least one of the following criteria:

• You are classified as a New Entrant. This means you are under the age of 26, currently studying in the UK or a recent graduate in the UK (Please read more about the New Entrant criteria: https://www.gov).

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