
Thermo Fisher Scientific, a worldwide leader in serving science, is currently inviting applications for the position of Medical Writer within its Clinical Research division. Reflecting the company’s commitment to modern work environments and accessing global talent, this high-impact role is being offered as a fully remote position, allowing the successful candidate to work from anywhere.
The Core Mission and Values
Thermo Fisher Scientific operates with a unified mission to enable customers to make the world healthier, cleaner, and safer. The company’s vibrant culture is built on a core set of values: Integrity, Intensity, Innovation, and Involvement. Employees work collaboratively to accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics, deliver innovative technologies to market, and increase laboratory productivity. Every team member, regardless of role, contributes directly to this mission on a daily basis.
The Role: Medical Writer in Clinical Research
The newly advertised position of Medical Writer is a high-quality medical and scientific writing role. It spans the entire document lifecycle, from early planning and coordination through to the delivery of final drafts for both internal and external clients. The successful candidate will be at the forefront of innovation, supporting effective and efficient scientific communication that underpins operational excellence within the clinical research process.
Key Responsibilities and What You’ll Do:
The role is multifaceted and offers significant opportunities for professional growth. Key responsibilities include:
- Primary Authorship: Serving as the lead author for routine clinical documents such as Clinical Study Reports (CSRs) and Study Protocols. This involves summarizing complex data from clinical studies into clear, concise, and scientifically accurate narratives.
- Complex Document Support: Depending on experience and capability, the Medical Writer may assist with more complex clinical, scientific, and program-level documents. This includes, but is not limited to, Investigator Brochures (IBs), Investigational New Drug (IND) applications, and Marketing Authorization Applications (MAAs).
- Quality and Compliance: Ensuring unwavering compliance with rigorous quality processes and regulatory requirements for all assigned documents. The writer may also assist in determining best practices, methods, and techniques to achieve optimal results.
- Program Management Activities: The role can extend into program management, including duties such as assisting with the development of timelines, budgets, and forecasts for assigned deliverables.
- Team Representation: Actively representing the Medical Writing department at various critical stages, including project launch meetings, review meetings, and overall project team meetings.
Education and Experience Requirements
Thermo Fisher Scientific is seeking candidates who possess a solid foundation in science and practical experience in the field. The requirements are as follows:
- Education: A Bachelor’s degree in a scientific discipline or an equivalent and relevant formal academic/vocational qualification is required.
- Experience: Candidates must demonstrate previous experience that provides the knowledge, skills, and abilities necessary to perform the job effectively. This is typically comparable to 3+ years of related experience. (Note: Years of experience are used as a typical guideline and not the sole determinant for selection or job classification.)
- Preferred Industry Experience: Previous experience working within the pharmaceutical or Contract Research Organization (CRO) industry is preferred.
- Writing Advantage: Prior experience in scientific writing is considered advantageous.
Knowledge, Skills, and Abilities for Success
To excel in this fully remote role, the ideal candidate must possess:
- Solid Medical Writing Skills: Including exceptional grammatical, editorial, and proofreading capabilities.
- Data Interpretation: The ability to interpret and present complex data accurately and concisely.
- Organizational Prowess: Effective administrative, organizational, and planning skills, combined with acute attention to detail and quality.
- Independence and Teamwork: The ability to work on one’s own initiative and collaborate effectively within a multidisciplinary team.
- Communication Skills: Strong oral and written communication skills are essential for both internal collaboration and client interaction.
- Regulatory Knowledge: A good understanding of regulatory documentation and the overall drug development process.
- Judgment and Decision-Making: Great judgment and robust decision-making skills.
- Computer Proficiency: Good computer skills, including proficiency with client templates, document management systems, and relevant applications such as Microsoft Excel and Outlook.
Why Join Thermo Fisher Scientific?
Joining Thermo Fisher Scientific means becoming part of a global team that genuinely values passion, innovation, and an unwavering commitment to scientific excellence. Employees work in a collaborative and developmental environment where their contributions truly make a difference in advancing science and improving lives. This specific fully remote role offers the added benefit of flexibility and work-life balance while remaining connected to a world-class scientific community.
Application Details
- Job ID: R-01366925
- Job Type: Full-time
- Category: Clinical Research
- Remote: Fully Remote
Interested and qualified candidates are encouraged to apply directly through the Thermo Fisher Scientific careers portal using the provided Job ID. Result-awaited candidates are not eligible to apply. No TA/DA will be paid for attending any potential interview, and only shortlisted candidates will be contacted.
This recruitment initiative aligns with Thermo Fisher Scientific’s ongoing mission to foster innovation by accessing diverse talent, regardless of location, to accelerate the pace of life sciences research and development globally.
