Thermo Fishers Hiring for Pharmacovigilance & Clinical Data Management | 0 – 4 Years

Thermo Fisher Scientific is hiring for two positions in India: FSP – Associate Safety Specialist and Clinical Data Associate I (CDA I). Both are full-time positions, with remote work arrangements listed in the job descriptions.

The Associate Safety Specialist role focuses on pharmacovigilance and drug safety activities, while the Clinical Data Associate I role involves clinical data cleaning, discrepancy resolution, and query management.

Thermo Fisher Scientific Recruitment 2026: Job Details

Positions Available

1. FSP – Associate Safety Specialist

The Associate Safety Specialist position involves day-to-day pharmacovigilance activities in a regulated environment, including adverse event processing, case review, safety assessment, follow-up, and regulatory safety reporting.

Job details

Responsibilities

• Perform day-to-day pharmacovigilance activities.
• Collect, monitor, assess, evaluate, research, and track safety information.
• Enter adverse event data and perform coding and assessment activities.
• Review cases for quality, consistency, and accuracy, including peer reports.
• Conduct case follow-ups and track safety reports.
• Prepare and maintain regulatory safety reports.
• Review pharmacovigilance publications and relevant regulatory information.
• Collaborate with project teams, clients, investigators, adverse event reporters, and third-party vendors.
• Participate in on-call duties for projects requiring 24-hour case intake coverage.

Eligibility and qualifications

• Bachelor’s degree or equivalent relevant academic or vocational qualification.
• Previous experience comparable to 0–2 years.
• Understanding of medical terminology and applicable therapeutic areas.
• Ability to work in a regulated environment and meet strict deadlines.

Required skills

• Critical thinking and problem-solving.
• Strong written and verbal communication skills.
• Good English proficiency and paraphrasing skills.
• Computer literacy and ability to work across multiple databases.
• Familiarity with Microsoft Outlook, Word, and Excel.
• Attention to detail and understanding of regulatory compliance.
• Task prioritization and teamwork.
• Ability to maintain professionalism in challenging situations.

2. Clinical Data Associate I (CDA I)

The Clinical Data Associate I position focuses on entry-level clinical data cleaning activities to support the assessment of the safety and efficacy of investigational products and medical devices. The role requires accuracy and adherence to Good Clinical Practice (GCP), standard operating procedures (SOPs), and work practice documents.

Job details

Responsibilities

• Identify, resolve, and update clinical data discrepancies.
• Make changes to the data management database when required.
• Generate, track, and resolve data clarification requests and queries.
• Implement Case Report Form (CRF) designs using an identified graphic design package when required.

Eligibility and qualifications

• High/secondary school diploma or equivalent, with relevant academic or vocational qualification.
• At least four years of comparable experience.
• Technical positions may require a certificate.
• Understanding of project protocols and the Data Validation Manual.

Required skills

• Strong attention to detail and numerical accuracy.
• Good written and verbal communication skills.
• Strong English language and grammar skills.
• Analytical thinking and problem-solving.
• Ability to use interactive computer programs.
• Knowledge of regulatory guidelines, global SOPs, and client expectations.
• Ability to maintain confidentiality of clinical and proprietary data.
• Flexibility, adaptability, and teamwork.
• Ability to work under direct supervision and exercise sound judgment.