Thermo Fisher Scientific Hiring Safety Specialist in Pharmacovigilance (Work From Home)
About Company:
Our clinical research services team is dedicated to developing cures for the world’s most challenging health concerns. As part of the PPD® clinical research portfolio within our global CRO, we lead in clinical research and drug development.
Position Name:
Safety Specialist III – Pharmacovigilance
Organization:
Thermo Fisher Scientific
Qualifications:
- B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Lifesciences
Experience:
- 1 to 2 Years
Salary:
- ₹4.8 Lakhs to ₹6.5 Lakhs
Location:
- Work From Home
Job Details:
Job Title | Safety Specialist III – Pharmacovigilance |
---|---|
Job ID | R-01243764 |
Job Type | Full-time |
Category | Clinical Research |
Location | Remote, India |
Responsibilities:
Responsibilities | Details |
---|---|
Pharmacovigilance Activities | Perform day-to-day PV tasks: collection, monitoring, assessment, evaluation, and tracking. |
Collaboration | Collaborate with project team members, clients, investigators, adverse event reporters. |
Leadership | Operate in a lead capacity, develop procedural documents, mentor less experienced staff. |
Audits | Prepare for and attend audits as required. |
Regulatory Updates | Stay updated on regulations, practices, and proposals by reviewing relevant publications. |
Medical Understanding | Maintain understanding of therapeutic areas and disease states. |
Quality Review | Review cases for quality, consistency, and accuracy, including peer report reviews. |
Project Coordination | Handle project implementation, client presentations, and review metrics and budgets. |
Literature Surveillance | Assess and peer review literature for adverse events and safety information. |
Primary Contact | Serve as the main contact for literature projects of varying complexity. |
Compliance | Ensure tasks adhere to company policies and regulations. |
Departmental Initiatives | Participate in departmental initiatives and inspections. |
Skills and Competencies:
- Strong analytical and problem-solving skills.
- Excellent written and oral communication skills.
- Proficiency with PV databases and IT applications.
- Ability to work effectively in a remote, team-oriented environment.
- Strong organizational and coordination skills.
- Knowledge of therapeutic areas and disease states relevant to current projects.
Qualifications:
- Relevant Bachelor’s or advanced degree in life sciences, pharmacy, nursing, or a related field.
- Thorough understanding of global pharmacovigilance regulations and guidelines.
How to Apply:
Click the “Apply Now” button to start your application process.