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Medical Consultant

Thermo Fisher Scientific
Thermo Fisher Scientific
2+ years
Not Disclosed
Hyderabad
10 May 12, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title:

Pharmacovigilance Physician

Work Schedule:

Third Shift (Night Shift)

Work Mode:

Office-Based

Company:

Thermo Fisher Scientific


About Thermo Fisher Scientific

Thermo Fisher Scientific is a global leader in serving science, dedicated to enabling customers to make the world healthier, cleaner, and safer. Through its PPD clinical research portfolio, the company supports clinical trials and drug development programs across more than 100 countries, delivering innovative solutions in laboratory services, digital technologies, and decentralized clinical trials.

For more information, visit: Thermo Fisher Scientific


Job Summary

We are seeking an experienced and highly motivated Pharmacovigilance Physician to provide medical oversight and scientific expertise for pharmacovigilance activities across the pharmaceutical product lifecycle. The role involves safety data review, signal detection, regulatory reporting, risk management, and collaboration with global clients and internal teams to ensure compliance with regulatory standards and patient safety requirements.

The ideal candidate should possess strong clinical expertise, excellent analytical skills, and in-depth knowledge of global pharmacovigilance regulations and drug safety processes.


Key Responsibilities

  • Manage medical and pharmacovigilance activities for assigned projects across the pharmaceutical product lifecycle.

  • Ensure compliance with company SOPs, client directives, ICH guidelines, GCP standards, and global regulatory requirements.

  • Perform medical review and assessment of Serious Adverse Events (SAEs), Individual Case Safety Reports (ICSRs), and adverse events of special interest.

  • Conduct causality assessments, seriousness evaluations, expectedness review, and MedDRA coding verification.

  • Support preparation and review of safety documents including PSURs, PBRERs, DSURs, Risk Management Plans (RMPs), REMS, CSRs, and CTD modules.

  • Participate in safety signal detection, benefit-risk evaluation, and safety investigations.

  • Review literature, aggregate safety data, coding listings, and safety databases to identify potential safety concerns.

  • Provide medical consultation and therapeutic training to project teams and clients.

  • Attend sponsor meetings and present pharmacovigilance-related findings and recommendations.

  • Support regulatory submissions, dossier maintenance, and labeling updates.

  • Mentor and guide junior staff members within the pharmacovigilance team.


Required Qualifications

  • MD / MBBS or equivalent medical qualification.

  • MBBS candidates should possess a minimum of 2 years of clinical experience.

  • Active medical licensure preferred.


Experience Requirements

  • Minimum 2 years of clinical or pharmacovigilance-related experience.

  • Experience in a Contract Research Organization (CRO), pharmaceutical company, clinical research environment, or drug safety function preferred.

  • Experience as a Principal Investigator or in clinical safety/pharmacovigilance activities will be an added advantage.


Required Skills & Competencies

  • Strong clinical knowledge with high attention to patient safety and quality standards.

  • Excellent understanding of pharmacology, physiology, and drug development processes.

  • Good knowledge of FDA, EMA, ICH, and GCP guidelines.

  • Familiarity with safety databases, MedDRA terminology, biostatistics, data management, and clinical operations.

  • Strong analytical, problem-solving, organizational, and multitasking skills.

  • Excellent written and verbal communication skills in English.

  • Ability to work independently and manage sensitive information effectively.

  • Strong interpersonal, collaboration, mentoring, and stakeholder management skills.

  • Proficiency in standard computer applications and reporting tools.


Working Environment

  • Office-based work environment with standard office equipment exposure.

  • Occasional domestic and international travel may be required.


Why Join Thermo Fisher Scientific?

  • Opportunity to work with a globally recognized leader in life sciences and clinical research.

  • Exposure to global clinical trials and innovative healthcare solutions.

  • Collaborative and growth-oriented work culture.

  • Opportunity to contribute to life-changing therapies and global patient safety initiatives.