HEOR Writer

CompanyJohnson & Johnson

LocationHigh Wycombe, England, United Kingdom

Posted At1/23/2026

UK Visa Sponsorship Analytics

Occupation Type

Authors, writers and translators

Occupation Code Skill LevelMedium Skilled

Sponsorship Salary Threshold

£41,700 (£21.38 per hour)

Standard minimum applies

Above analytics are generated algorithmically based on job titles and may not always be the same as the company's job classification. You can also check detailed occupation eligibility, and salary criteria on our UK Visa Eligible Occupations & Salary Thresholds page.

Disclaimer: Hunt UK Visa Sponsors aggregates job listings from publicly available sources, such as search engines, to assist with your job hunting. We do not claim affiliation with Johnson & Johnson. For the most up-to-date job details, please visit the official website by clicking "Apply Now."

Description

HEOR Writer

Location: High Wycombe - Hybrid working 3 days a week on site

Duration: 12 months

Hours: 37

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.

Role purpose:

Imagine your next project working as a HEOR Writer for Johnson & Johnson. Johnson and Johnson Innovative Medicine UK is currently recruiting a Health Economics, Market Access and Reimbursement (HEMAR) Writer located in High Wycombe in the UK to support the delivery of accelerated, broad market and patient access and funding for our key brands. The successful candidate will play a key role as part of the HEMAR team working with a group of market access and health economics specialists as well as extended interactions with Medical Affairs and external vendors.

The role objectives are to deliver high quality HTA dossiers and real world evidence documentation to ensure high quality and successful UK HTA submissions, and to provide internal expertise to ensure high quality evidence generation project delivery. The role reports into the Head of HEMAR with a dotted line to the Head of Health Outcomes, they will define the strategic needs for the role in regard to key HTA and RWE deliverables.

The goal of the HEMAR department is to optimise the value of both the Company and its products, through the development of a positive external image perceived by payers. This is done by effectively communicating the innovative value the Company and its medicines provide to patients, to the National Health Service, and to the community as a whole.

roles and responsibilities

Take ownership of the planning, writing and editing of Health Technology Assessment submission documents, in collaboration with HEMAR brand team to ensure delivery of high quality submissions to national and local health technology assessment organisations, such as NICE and, SMC to achieve positive recommendations.

Work as part of a collaborative internal HTA team with relevant HEMAR, commercial and medical affairs colleagues to understand the overall product and submission strategy around relevant products

Contribute to the planning, writing and editing of RWE study documentation and reporting e.g. study synopses, protocols, reports and manuscripts for internal and external stakeholders to help implement studies which meet evidence gaps to build positive and compelling commercial opportunities, including taking projects through internal approval processes

Take a leading role in RWE project team to support study and analysis plan design as well as data source selection and contribute to management of internal compliance processes

Demonstrate innovation in use of in-house artificial intelligence to efficiently prepare HTA and RWE documentation

Prepare materials for external consultations such as ad boards or HTA policy engagement

Writing and editing patient access documents to ensure that they are accurate, clearly written, and conform to the editorial in-house style

Analyse and summarise clinical studies, data and information, in order to apply this to the strategic positioning of J&J IM products, within the context of the market and the healthcare environment

how to succeed

Demonstrable experience in writing UK HTA submission documents, real world evidence protocols and epidemiology publications necessary
Specific experience in the following is desirable:
Scientific abstract and manuscript writing
NICE HTA Document A and Document B, as well as responses to the EAG report and NICE technical engagement
SMC NPAF and response to clarification questions
Real world evidence study design
Familiarity with UK data sources
RWE methods protocol and statistical analysis plan design and writing
Patient Access policy communications
Systemic literature reviews
A graduate degree in a relevant life sciences field or communications field would be considered beneficial (for example biology, economics, statistics)

benefits

This role offers a very competitive hourly rate. This contract will run for 12 months and has a strong chance of extension.

you are welcome here

Johnson & Johnson is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

about Johnson & Johnson Innovative Medicine

Patients inform and inspire our science-based innovations, which continue to change and save lives. Applying rigorous science and compassion, we confidently address some of the most complex diseases of our time and unlock the potential medicines of tomorrow.

Our diverse portfolio spans multiple therapeutic areas — Oncology, Immunology, Neuroscience, Cardiovascular, Pulmonary Hypertension, and Retina.

We are continuously working to develop treatments, aspiring to find cures, pioneering the path from lab to life, and championing patients every step of the way.

application process

We do not accept applications via email.
The pay rate for this role will depend on how you are paid.

Diversity, Equity & Inclusion

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.