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)