Medical Writing / Clinical Research

Thermo Fisher Scientific is seeking applications from qualified professionals for the role of Associate Medical Writer. This is a full-time remote position based in India, offering an opportunity to work on global medical writing projects that support clinical research and pharmaceutical development.

Candidates with a background in life sciences and experience in scientific or medical documentation are encouraged to apply.

Position Details

• Company: Thermo Fisher Scientific

• Job Role: Associate Medical Writer

• Location: Mumbai, India (Remote)

• Employment Type: Full-Time

• Work Mode: Fully Remote

• Experience Required: 1–3 Years

• Schedule: Monday to Friday

Role Overview

The Associate Medical Writer will contribute to the creation, editing, and review of scientific and medical documents used throughout clinical research projects. The selected candidate will work with internal teams and external stakeholders to produce clear, accurate, and compliant documentation while ensuring project timelines and quality standards are met.

This role offers exposure to international clinical development programs and provides an opportunity to build expertise in medical communication within a globally recognized organization.

Key Responsibilities

• Prepare and revise informed consent forms, lay summaries, and other patient-focused documents.

• Assist in developing scientific and clinical research documents as required.

• Review documents to maintain quality, consistency, and regulatory compliance.

• Support project planning activities, including timelines and document coordination.

• Participate in project meetings and collaborate with multidisciplinary teams.

• Communicate effectively with internal departments and external clients.

• Ensure assigned documentation is completed accurately and delivered on schedule.

Eligibility Criteria

Applicants should possess:

• A Bachelor's degree in Pharmacy, Life Sciences, Biotechnology, or another relevant scientific discipline, or an equivalent qualification.

• Around 1 to 3 years of relevant professional experience.

• Experience in the pharmaceutical, biotechnology, or Contract Research Organization (CRO) industry will be an advantage.

• Previous exposure to medical or scientific writing is preferred but not mandatory.

Desired Skills

Successful candidates should demonstrate:

• Good scientific writing, editing, and proofreading skills.

• Ability to simplify and present scientific information accurately.

• Strong organizational and time management abilities.

• Excellent written and verbal communication skills.

• Basic understanding of clinical research documentation and drug development processes.

• Knowledge of Microsoft Office applications and document management systems.

• Ability to work independently while collaborating effectively with cross-functional teams.

• Strong attention to detail and commitment to maintaining documentation quality.

Work Environment

This is a fully remote role with a standard Monday-to-Friday work schedule. Depending on project requirements, occasional domestic or international travel may be required, along with flexibility to support business needs.

Why Consider This Opportunity?

Joining Thermo Fisher Scientific provides an opportunity to contribute to global healthcare initiatives while working in a collaborative and innovation-driven environment. Employees gain exposure to international clinical research projects, continuous learning opportunities, and a professional culture focused on scientific excellence and career growth.