We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics and increase laboratory productivity. With $1.4 billion invested annually in R&D, our collaborative and diverse teams have the resources they need to drive new discoveries and do cutting-edge research and develop important applications and tools that help millions of lives around the world.
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
Evidera’s Value Communications Solutions team interprets and communicates the clinical and economic evidence that our pharmaceutical/life sciences clients require to successfully market their products. Our services include dossiers and slide decks that provide healthcare decision-makers with the evidence they need to evaluate new medical treatments, targeted literature-based white papers on diseases and treatments, and reports from payer advisory boards.
Job Title: Market Access Writer I/II
Team: EMC – Market Access Communications, Evidera
Location: Poland (Remote)
At Evidera, a Market Access Writer I will carry out the following duties:
Work with project teams to support the development of market access deliverables for pharmaceutical sector clients, including Global Value Dossiers, Payer Value Platforms, and Health Technology Assessment submission documents.
Develop content for key deliverables, based on relevant scientific literature and any other source materials shared by clients with the study team.
Conduct literature searches and screen results to identify relevant studies.
Manage referencing resources, to ensure that all sources are cited to the required standard.
Self-review submitted work to ensure high quality standards are met and maintained.
Work in a self-directed manner, under the guidance of a project manager, to ensure on-time delivery of content.
Manage workload effectively, to enable completion of work on-time despite multiple overlapping deadlines during key periods.
Develop additional skills through on-the-job training, including client communication and interaction, task management and build familiarity with key internal systems and platforms.
Personal Skills & Competencies:
Ability to understand and clearly convey complex clinical, economic, and commercial information, after receiving appropriate training on new content areas
Research and analysis skills, e.g., ability to undertake reviews of the scientific literature
Willingness to learn about HTA requirements
Familiarity with Microsoft Word, PowerPoint, and Excel
Attention to detail
Strong time management skills and ability to work simultaneously on multiple projects
Comfortable with working with deadlines
Ability to work in teams
It is helpful, but not essential, to have:
Knowledge of the pharmaceutical industry and drug development process
Familiarity with clinical trials and basic biomedical statistics
Understanding of market access and health economics
Experience with bibliographic referencing software
Education, Professional Skills & Experience:
BSc or advanced degree in life sciences, health economics, or a clinical discipline is preferred. Clinical degrees in nursing, nutrition, or other health professions will also be considered.
Benefits
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
EEO & Affirmative Action Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.