work from home Medical Writer vacancies at Thermo Fisher Scientific

Thermo Fisher Scientific Hiring FSP Medical Writer | 2+ Years Experience | Fully Remote | Bangalore

Thermo Fisher Scientific is expanding its Clinical Research team and is currently hiring for the position of FSP Medical Writer under its PPD clinical research portfolio. This is a full-time, fully remote opportunity based in Bangalore, Karnataka, India. The vacancy is open to professionals with at least 2 years of regulatory writing experience in the pharmaceutical or CRO industry. Candidates with expertise in clinical documentation, regulatory submissions, and structured content authoring systems are strongly encouraged to apply.

This opportunity is ideal for life sciences graduates seeking medical writing jobs in India, remote clinical research jobs, and regulatory affairs careers within a global contract research organization. If you are looking to advance your career in drug development, pharmacovigilance documentation, and clinical trial reporting, this role offers strong long-term growth potential.

Company Overview

Thermo Fisher Scientific is one of the world’s leading biotechnology and life sciences companies, supporting pharmaceutical innovation, laboratory research, and global healthcare advancement. Through its PPD clinical research services division, the company delivers comprehensive contract research organization (CRO) solutions across more than 100 countries.

The organization supports the full drug development lifecycle, from early-phase clinical trials to regulatory submissions and post-marketing surveillance. Its teams work across laboratory services, decentralized clinical trials, digital research platforms, regulatory consulting, and medical writing services.

With over 100,000 professionals worldwide, Thermo Fisher Scientific operates with a strong focus on scientific integrity, regulatory compliance, and innovation. The PPD portfolio is recognized globally for delivering high-quality clinical research services to pharmaceutical, biotechnology, and healthcare companies. This credibility makes it a preferred employer for professionals seeking high-impact clinical research careers and remote medical writing opportunities.

The company emphasizes structured career progression, continuous learning programs, and global collaboration. Employees benefit from a stable work environment, competitive compensation, and strong exposure to international regulatory frameworks including US FDA, EMA, ICH, and other global health authorities.

Job Role & Responsibilities

The FSP Medical Writer will be dedicated to a client within the Functional Service Provider (FSP) model. The selected candidate will develop high-quality clinical and regulatory documents aligned with international regulatory standards and company compliance frameworks.

Core Responsibilities

• Draft and edit clinical study reports (CSRs), study protocols, investigator brochures, and regulatory submission documents.
• Prepare documentation supporting global regulatory submissions for pharmaceutical and biotechnology products.
• Ensure compliance with ICH guidelines, FDA regulations, EMA standards, and internal quality control systems.
• Collaborate with cross-functional teams including clinical operations, biostatistics, data management, pharmacovigilance, and regulatory affairs.
• Contribute to document strategy, structure, and content presentation to ensure clarity and scientific accuracy.
• Review documents prepared by peers and provide constructive feedback.
• Manage timelines, project deliverables, and client expectations within the FSP framework.
• Stay updated on evolving regulatory writing guidelines and structured content management practices.

Technical & Functional Expectations

• Experience with structured content authoring systems.
• Familiarity with automation tools and AI-driven content creation.
• Understanding of Natural Language Generation (NLG) platforms preferred.
• Strong knowledge of clinical trial processes and drug development lifecycle.
• Awareness of safety writing such as DSUR (Development Safety Update Reports) is advantageous.

This role directly contributes to the successful approval of life-changing therapies by ensuring clinical documentation meets global regulatory standards. Medical writing professionals in this position play a critical role in accelerating regulatory review timelines and maintaining data integrity in clinical research.

Eligibility & Qualifications

Thermo Fisher Scientific is seeking candidates with a strong academic foundation in life sciences and proven regulatory writing experience.

Educational Requirements

Bachelor’s degree in a scientific discipline or equivalent qualification is mandatory. An advanced degree is preferred.

Relevant academic backgrounds include:

B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, Biomedical Sciences, Nursing, Medicine, or other related healthcare and pharmaceutical sciences disciplines.

Experience Requirements

• Minimum 2+ years of regulatory writing experience.
• Experience within a pharmaceutical company or contract research organization.
• Exposure to clinical documentation and regulatory submissions.
• Experience in safety writing (DSUR) is beneficial.

Required Skills

• Strong understanding of global regulatory guidelines.
• Excellent written and verbal communication skills.
• Ability to work independently in a fully remote environment.
• Strong project management and organizational skills.
• High attention to detail and document accuracy.
• Leadership capability to mentor junior medical writers when required.

Candidates seeking senior medical writing jobs, regulatory affairs roles, or CRO career growth opportunities will find this position aligned with long-term professional advancement.

Location & Salary

Location: Bangalore, Karnataka, India
Work Model: Fully Remote
Job Type: Full-Time
Work Schedule: Monday to Friday
Environment: Office-based (Remote setup)

Application Process

Interested candidates can apply directly through the official career portal using the link below:

Apply Here:
https://jobs.thermofisher.com/global/en/job/R-01343035/FSP-Medical-Writer

Applicants are advised to:

• Update their resume highlighting regulatory writing experience.
• Clearly mention experience with clinical study reports, protocols, and regulatory submissions.
• Include details about structured content management systems if applicable.
• Emphasize CRO or pharmaceutical industry exposure.

Shortlisted candidates will be contacted by the recruitment team for further evaluation.

Frequently Asked Questions (FAQs)

1. Is this role suitable for freshers?

No. A minimum of 2 years of regulatory writing experience in the pharmaceutical or CRO industry is required.

2. Is the job completely remote?

Yes. This is a fully remote opportunity, although the base location is Bangalore, Karnataka.

3. What kind of documents will the Medical Writer handle?

The role involves drafting clinical study reports, protocols, investigator brochures, and regulatory submission documents aligned with global regulatory standards.

4. Is safety writing experience mandatory?

Safety writing such as DSUR experience is advantageous but not mandatory.

5. What industries can candidates come from?

Candidates should have experience in pharmaceutical companies, biotechnology firms, or contract research organizations.

6. What career growth can be expected?

Professionals can progress into senior medical writer, regulatory affairs specialist, documentation lead, or clinical research leadership roles.

7. What qualifications are accepted?

B.Pharm, M.Pharm, Pharm.D, MSc, Biotechnology, Microbiology, Biochemistry, Clinical Research, Biomedical Sciences, and related life sciences degrees are accepted.

Company	Thermo Fisher Scientific
Vacancies	FSP Medical Writer
Required Education	B.Pharm, M.Pharm, Pharm.D, BSc, MSc, Biotechnology, Microbiology, Biochemistry, Clinical Research, Biomedical Sciences or related life sciences degree
Experience	Minimum 2+ years regulatory writing experience in pharmaceutical or CRO industry