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Thermo Fisher Scientific Hiring for Medical Writing, Clinical Trial Management and Site Payments | Remote

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B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences. Finance, Business, Ph.D, Medicine or Relvant Degree

Remote, India; Mumbai, India

3 - 10 Years

Verified Job

Online Application
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Thermo Fisher Scientific is hiring for three positions in India: Principal Medical Writer, Clinical Trial Manager – FSP, and Site Payments Associate II – FSP. The openings include remote opportunities in India and a Clinical Trial Manager position based in Mumbai. Candidates can review the role-specific responsibilities and eligibility requirements before applying through the official careers portal.

Thermo Fisher Scientific Recruitment 2026: Job Details

Job DetailInformation
CompanyThermo Fisher Scientific
Total Positions3
Employment TypeFull-time
Work ScheduleStandard, Monday to Friday
Job LocationsRemote, India; Mumbai, India
Work ArrangementFully Remote for all three listings
Job CategoriesMedical Writing, Clinical Research, Site Payments

1. Principal Medical Writer

Location: Remote, India
Job Type: Full-time
Requisition ID: R-01369790

Job Responsibilities

  • Research, write and edit clinical study reports and study protocols.
  • Summarize data from clinical studies.
  • Author complex clinical, scientific and program-level documents, including Investigator’s Brochures (IBs), Investigational New Drug (IND) applications and Marketing Authorisation Applications (MAAs).
  • Review routine and complex documents for quality and accuracy.
  • Provide training, guidance and mentorship to junior medical writers and program managers.
  • Ensure compliance with document quality processes and regulatory requirements.
  • Develop best practices and lead process improvement initiatives.
  • Support project timelines, budgets, forecasts and client presentations when serving as backup program manager.
  • Participate in project launch meetings, review meetings and project team meetings.

2. Clinical Trial Manager – FSP

Location: Mumbai, India
Job Type: Full-time
Requisition ID: R-01370563

Job Responsibilities

  • Manage clinical operational and quality aspects of assigned clinical studies in compliance with ICH Good Clinical Practice (GCP).
  • Develop monitoring plans, monitoring guidelines and clinical study documents.
  • Support the preparation and maintenance of the Trial Master File (TMF).
  • Coordinate with clinical teams and other departments to meet project timelines and quality requirements.
  • Monitor clinical activities, review monitoring visit reports and support case report form (CRF) collection and query resolution.
  • Coordinate study start-up activities and ethics committee and regulatory submissions, where applicable.
  • Communicate with clinical study sites regarding protocols, patient participation and study documentation.
  • Manage clinical resources, clinical activity timelines and project deliverables.
  • Support clinical team meetings, training and standardized monitoring processes.
  • Assist with project financials, forecasts and resource planning when required.

Eligibility and Qualifications

  • Bachelor’s degree or equivalent, with a relevant formal academic or vocational qualification.
  • More than one year of experience in a Clinical Trial Manager (CTM) role, with the job description also requiring two or more years of experience in its stated CTM experience criterion.
  • Hands-on experience in onsite monitoring and clinical trial management.
  • Candidates must be based in Mumbai or nearby locations.
  • Hands-on experience with Informed Consent Forms (ICFs), DCGI submissions, import/export processes and Ethics Committee/Institutional Review Board (EC/IRB) submissions.
  • Experience negotiating site contracts and scheduling and leading meetings with DCGI or other regulatory authorities.
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Required Skills

  • Knowledge of ICH-GCP and relevant regulatory guidelines.
  • Clinical monitoring and trial management expertise.
  • Leadership, team coordination and mentoring skills.
  • Planning, prioritization and organizational skills.
  • Problem-solving and decision-making abilities.
  • Effective written and verbal communication skills in English.
  • Familiarity with project budgeting, forecasting and resource management.
  • Attention to detail and proficiency with Microsoft Outlook, Excel and Word.

3. Site Payments Associate II – FSP

Location: Remote, India
Job Type: Full-time
Requisition ID: R-01369690

Position Overview

Thermo Fisher Scientific is recruiting for the Site Payments Associate II – FSP position

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APPLICATION DETAILS

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