Thermo Fisher Scientific, a global leader in clinical research and life sciences, has announced multiple openings across India for medical writing, pharmacovigilance, and project management professionals. These roles — from Associate Medical Writer (FSP Medical Writing) to Associate Manager – Safety Data and PV Systems — offer remote and onsite options, competitive pay, and a chance to work with the world’s leading healthcare innovation company.
Whether you are a fresher in medical writing or an experienced pharmacovigilance specialist, Thermo Fisher’s latest recruitment drive provides opportunities to build a fulfilling scientific career.
🧠 1. Associate Medical Writer – FSP Medical Writing (Remote, India)
Type: Full-time | Remote: Yes | Experience: 0–2 years
Key Responsibilities
- Assist in drafting clinical study reports, protocols, and narratives.
- Support regulatory and clinical documentation preparation.
- Ensure compliance with internal quality standards and regulatory guidelines.
- Participate in team and project review meetings.
Qualifications
- Bachelor’s degree in a scientific discipline (advanced degree preferred).
- 0–2 years’ experience; scientific writing background is a plus.
- Strong English grammar, data interpretation, and organizational skills.
Ideal For
Fresh graduates or entry-level professionals looking to start a career in medical and regulatory writing with Thermo Fisher’s PPD Clinical Research Services.
🩺 2. ICF Medical Writing Program Manager (Remote, India)
Type: Full-time | Remote: Yes | Experience: 8+ years
Key Responsibilities
- Lead global medical writing programs focused on Informed Consent Forms (ICFs).
- Manage client relationships, timelines, budgets, and program quality.
- Mentor junior staff and ensure compliance with writing and regulatory processes.
- Collaborate with internal and external stakeholders to ensure project excellence.
Qualifications
- Bachelor’s or Master’s degree (Life Sciences preferred).
- Minimum 8 years’ experience in medical writing or clinical project management.
- Expertise in global regulatory documentation and leadership skills.
💊 3. Associate Manager – Safety Data and PV Systems (Remote, India)
Type: Full-time | Remote: Yes | Experience: 7+ years
Key Responsibilities
- Lead safety data management and pharmacovigilance system operations.
- Manage Argus Safety system configuration, reporting, and validation.
- Support regulatory compliance and safety signal management.
- Collaborate with global safety, regulatory, and IT teams.
Qualifications
- Bachelor’s degree in Life Sciences or IT.
- At least 7 years’ experience in pharmacovigilance or clinical research.
- Hands-on experience with Argus or ArisG systems.
- Strong knowledge of PV regulations (FDA, EMA, ICH).
🧩 4. Associate Manager – Project Support Services (Bengaluru, India)
Type: Full-time | Onsite: Yes | Experience: 0–5 years
Key Responsibilities
- Manage project staff, SOPs, and quality initiatives.
- Oversee study startup, maintenance, and close-out activities.
- Train and mentor research and clinical teams.
- Support project bids, budgets, and timelines.
Qualifications
- Bachelor’s degree in Life Sciences or related field.
- 0–5 years’ experience in clinical research or project management.
- Strong leadership and communication skills.
🎁 What Thermo Fisher Offers
- Competitive salary packages (₹6 LPA–₹28 LPA based on role).
- Fully remote and flexible working options.
- Global learning and development programs.
- Inclusive, diverse, and collaborative work culture.
- Career growth across research, writing, and safety domains.
📝 How to Apply
Application Link for Associate Medical Writer – FSP Medical Writing (Remote, India)
Application Link for ICF Medical Writing Program Manager (Remote, India)
Application Link for Associate Manager – Safety Data and PV Systems (Remote, India)
Application Link for Associate Manager – Project Support Services (Bengaluru, India)
