Soterius, a leading name in healthcare, is offering an exciting opportunity to join its team as a
Senior Associate in Pharmacovigilance. This full-time position is based in
New Delhi, and the ideal candidates will have a strong background in pharmacovigilance, drug safety, and quality control.
Position Overview
- Job Title: Senior Associate – Pharmacovigilance
- Department: Pharmacovigilance
- Job Location: New Delhi, India
- Job Type: Full-time (Work from Office)
- Experience Required: Minimum 1 year in Quality Control (QC)
- Positions Available: 4
Job Responsibilities
As a Senior Associate in Pharmacovigilance at Soterius, you will play a critical role in drug safety and regulatory compliance. Your key responsibilities include:
- Monitoring and Reporting: Collecting and analyzing data related to drug safety and adverse event reports.
- Regulatory Compliance: Ensuring that all pharmacovigilance activities comply with regulatory requirements and global standards.
- Case Management: Preparing and submitting individual case safety reports (ICSRs) to the relevant regulatory bodies.
- Team Collaboration: Working closely with cross-functional teams such as clinical research, medical affairs, and regulatory departments to maintain high safety standards.
- Quality Assurance: Conducting regular audits and quality checks to ensure data accuracy and regulatory compliance.
Eligibility Criteria
To be considered for this position, you must meet the following qualifications:
- Educational Qualification: M Pharmacy, B Pharmacy, BDS, or PharmD is required.
- Experience: At least 1 year of experience in Quality Control (QC) or related fields.
- Knowledge of global pharmacovigilance regulations and adverse event reporting processes.
- Proficiency in safety databases and MS Office.
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Soterius Job Opportunity for Pharmacovigilance - Senior Associate[/caption]
How to Apply
If you meet the qualifications and are excited about this opportunity, please submit your resume to the following email address:
https://pharmastuff.org.in/job/soterius-pharmacovigilance-senior-associate