Market Access Writer II

Work Schedule

Environmental Conditions

Job Description

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)

Position Overview:

This is a team-based, collaborative writing and research role in which you will apply scientific and communication expertise to projects that are carried out on behalf of a mix of pharmaceutical and biotech clients and targeted towards a variety of end audiences. These engagements cover a wide range of product types, therapeutic areas and types of assignment.

The Market Access Writer is a highly motivated, detail-oriented, and an organized self-starter who works well both independently and in teams. Enthusiasm for a professional writing and market access career and excellent verbal and written communication skills are essential.

The individual will be part of the Market Access Communications team which is itself part of the wider Evidence Synthesis, Modeling & Communication (EMC) unit at Evidera. Our organisation offers many opportunities for professional and personal development and we encourage all of our staff to proactively tailor their career path.

Essential Duties and Responsibilities (other duties may be assigned):

• Writing fully referenced content, for local health technology assessment (HTA) dossiers such as National Institute for Health and Care Excellence (NICE), Scottish Medicines Consortium (SMC) Academy of Managed Care Pharmacy (AMCP), and global value dossiers, based on published clinical, scientific, and pharmacoeconomic material

• Carry out targeted literature reviews

• Value message development and testing

• Review of HTA assessments

• Developing simple visuals and graphics (e.g., in Excel or PowerPoint)

• Editing, quality assurance, and formatting

• Interaction with clients to understand their expectations and to receive their feedback

• Daily communication and teamwork with colleagues in the Market Access Communications team

• Learning the basic methods and approaches employed by the Evidence Synthesis and Modelling teams within EMC

• Workload management to meet internal and client-driven deadlines

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.

[New graduates without relevant industry experience would be considered at MAWI

Candidates with 1-3 years’ relevant industry experience would be considered as MAWII]

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

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.

Apply today! http://jobs.thermofisher.com

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.