Medical Writer Job at Thermo Fisher
Are you looking for a Medical Writing Job in the pharmaceutical or clinical research industry? Thermo Fisher Scientific is hiring an Associate Medical Writer to support the preparation of high-quality medical and scientific documents.
The selected candidate will assist with researching, writing, editing, reviewing, and delivering documents for internal and external clients. Professionals with strong scientific writing, proofreading, data-interpretation, and regulatory-documentation skills are encouraged to apply.
- Job Title: Associate Medical Writer
- Company: Thermo Fisher Scientific
- Qualification: Bachelor’s degree in a scientific discipline or equivalent
- Experience: 1–3 years
- Work Schedule: Monday–Friday
- Work Environment: Office-based
- Industry Experience: Pharmaceutical or CRO experience is advantageous
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is a global leader in serving science, with annual revenue exceeding $40 billion. Its mission is to enable customers to make the world healthier, cleaner, and safer.
The company supports customers involved in life-sciences research, analytical problem-solving, laboratory productivity, diagnostics, and the development and manufacturing of innovative therapies.
Thermo Fisher Scientific’s portfolio includes brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
Job Description
As an Associate Medical Writer, the candidate will assist in preparing high-quality medical and scientific content, from initial planning and coordination through the delivery of final drafts.
The role involves collaborating with internal and external clients to support clear, accurate, and efficient scientific communication. The successful candidate will contribute to operational excellence by ensuring that assigned documents meet applicable quality requirements.
Key Responsibilities
- Research, write, and edit routine medical and scientific documents.
- Assist in preparing informed consent forms.
- Develop lay summaries and other patient-centric documents.
- Support the preparation of complex clinical, scientific, and program-level documents when required.
- Ensure assigned documents comply with applicable quality processes and requirements.
- Assist with document planning, coordination, review, and final delivery.
- Support program-management activities when assigned.
- Help develop project timelines, budgets, and forecasts.
- Participate in project-launch meetings.
- Attend document-review and project-team meetings.
- Collaborate with internal and external clients throughout the document-development process.
- Deliver accurate, concise, and high-quality scientific content within established timelines.
Eligibility Criteria
- Education: Bachelor’s degree in a scientific discipline or an equivalent academic or vocational qualification.
- Experience: Approximately 1–3 years of relevant professional experience.
- Industry Experience: Previous experience in the pharmaceutical or CRO industry is advantageous.
- Writing Experience: Scientific or medical writing experience is advantageous.
A suitable combination of education, training, and directly related experience may also be considered sufficient to meet the requirements of the position.
Required Skills
- Basic medical and scientific writing abilities.
- Strong grammar, editing, and proofreading skills.
- Ability to understand and present complex scientific data accurately and concisely.
- Basic knowledge of regulatory documentation.
- Understanding of the drug-development process.
- Strong administrative, organizational, and planning abilities.
- Excellent attention to detail and commitment to quality.
- Ability to work independently and take initiative.
- Ability to collaborate effectively within a team.
- Effective written and verbal communication skills.
- Good judgment and decision-making abilities.
- Competent computer skills.
- Ability to work with document templates.
- Basic knowledge of document-management systems.
- Working knowledge of Microsoft Excel, Outlook, and other relevant applications.
Working Conditions
- The role is performed in an office environment.
- Employees may be exposed to standard electrical office equipment.
- Occasional travel to site locations may be required.
- The position may involve occasional domestic and international travel.
- Long or varied working hours may occasionally be necessary.
Why Join Thermo Fisher Scientific?
Thermo Fisher Scientific offers professionals an opportunity to work within a global organization focused on scientific excellence, collaboration, and innovation.
The company reports that it has supported the world’s top 50 pharmaceutical companies and more than 750 biotechnology organizations. Over the past five years, its teams have contributed to approximately 2,700 clinical trials across more than 100 countries.
Employees can collaborate with experienced professionals while contributing to projects that support pharmaceutical development, clinical research, diagnostics, and scientific advancement.
Apply for the Associate Medical Writer Job
This Associate Medical Writer Job at Thermo Fisher Scientific is an excellent opportunity for candidates with a scientific educational background and 1–3 years of relevant experience. Candidates with pharmaceutical, CRO, scientific-writing, or regulatory-documentation experience are encouraged to apply.
Pharmanika is a career information portal. Candidates should verify the eligibility criteria, job location, application deadline, and other details from the official Thermo Fisher Scientific job notification before applying.
