Thermo Fisher Scientific India Pvt Ltd is hiring B. Pharma/ M. Pharma/ B. Sc/ M. Sc as a Safety Specialist III – Apply Now

Welcome to an exciting career opportunity with Thermo Fisher Scientific India Pvt Ltd! We’re thrilled to announce that we are currently hiring for the position of Safety Specialist III. This role is open to talented individuals with backgrounds in B. Pharma, M. Pharma, B. Sc., M. Sc., or Pharma D.

If you’re passionate about ensuring safety in the pharmaceutical industry and are ready to take your career to the next level, then this could be the perfect opportunity for you. Join our team and make a meaningful impact in the world of healthcare and safety. Apply now to become a part of Thermo Fisher Scientific’s innovative and dynamic workforce!

Responsibility
As A Safety Specialist III At PPD, You Will Play A Crucial Role In Performing And Overseeing Day-To-Day Pharmacovigilance (PVG) Activities Within A Highly Regulated Environment. Your Responsibilities Will Include Collection, Monitoring, Assessment, Evaluation, Research, And Tracking Of Safety Information. You Will Collaborate Effectively With Various Stakeholders, Including Project Team Members, Client Contacts, Investigators, Adverse Event Reporters, And Third-Party Vendors.

Job Description
1. Independently Perform Day-To-Day PVG Activities, Including Participating In On-Call Duties For Specific Projects To Ensure 24-Hour Coverage For Case Intake From Investigative Sites.
2. Operate In A Lead Capacity, Providing Assistance In Developing Program And Departmental Procedural Documents, Preparing For And Attending Audits, And Mentoring Less Experienced Staff.
3. Stay Updated On Current Regulations, Practices, Procedures, And Proposals In Regulatory/Pharmacovigilance Publications And Maintain Medical Understanding Of Applicable Therapeutic Areas And Disease States.
4. Review Cases Entered For Quality, Consistency, And Accuracy, Including Peer Reports Review.
5. Responsible For Routine Project Implementation And Coordination, Such As Clinical Trials, Endpoint Assessment Committee/Data Safety Monitoring Committee, Including Presentations At 6. Client/Investigator Meetings And Review Of Metrics And Budget Considerations.

Qualifications:
1. Education And Experience: Bachelor’s Degree Or Equivalent, With 5+ Years Of Relevant Experience.
2. Knowledge, Skills, And Abilities:
3. Thorough Understanding Of Pathophysiology And Disease Processes.
4. Strong Knowledge Of Relevant Therapeutic Areas For Processing Adverse Events.
5. Excellent Critical Thinking And Problem-Solving Skills.
6. Proficient In Complex Clinical Study Administration, Including Budget Activities And Forecasting.
7. Excellent Oral And Written Communication Skills.
8. Good Command Of English And Ability To Translate Information Into Local Languages.
9. Proficient In Microsoft Office Products And Multiple Databases.
10. Thorough Understanding Of Global Regulatory Requirements.
11. Ability To Manage And Prioritize Tasks, Meet Strict Deadlines, And Work Effectively Within A Team.
12. Strong Attention To Detail And Ability To Maintain A Positive And Professional Demeanor In Challenging Circumstances.

Job Location: Hyderabad

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