Pharmacovigilance Associate (Freshers)
Location: Bhat, Ahmedabad, Gujarat, India
Company: Cadila Pharmaceuticals Ltd.
Department: Pharmacovigilance (PV)
Employment Type: Full-Time
Work Mode: On-Site
Role Summary
Cadila Pharmaceuticals is seeking enthusiastic and motivated BDS Freshers to join its Pharmacovigilance team. This role provides an excellent opportunity to build a career in Drug Safety and Pharmacovigilance while contributing to global patient safety initiatives.
The Pharmacovigilance Associate will be responsible for supporting adverse event case processing, safety data review, medical assessment, regulatory compliance activities, and pharmacovigilance operations in accordance with global regulatory requirements and company procedures.
This position offers hands-on exposure to drug safety surveillance, case management, medical coding, and safety reporting within a leading pharmaceutical organization.
Key Responsibilities
Individual Case Safety Report (ICSR) Processing
Review, assess, and process Individual Case Safety Reports (ICSRs).
Capture and document adverse event information accurately.
Ensure timely and complete case processing in compliance with regulatory requirements.
Maintain case quality and data integrity throughout the case lifecycle.
Case Intake & Safety Data Review
Receive and review safety information from various sources including:
Healthcare Professionals
Patients
Medical Literature
Regulatory Authorities
Company Sources
Verify completeness and accuracy of case information.
Identify reportable adverse events and safety information.
Medical Coding & Data Entry
Perform accurate data entry into Pharmacovigilance Safety Databases.
Support medical coding activities using:
MedDRA (Medical Dictionary for Regulatory Activities)
WHO Drug Dictionary (as applicable)
Ensure consistency and accuracy of coded medical information.
Safety Surveillance & Monitoring
Support ongoing monitoring of adverse drug reactions and safety signals.
Assist in identifying potential safety concerns and trends.
Contribute to activities related to drug safety surveillance and risk management.
Follow-Up Activities
Initiate follow-up requests for incomplete case information.
Coordinate with relevant stakeholders to obtain additional safety details.
Update safety cases with follow-up information received.
Regulatory Compliance
Ensure compliance with:
Good Pharmacovigilance Practices (GVP)
Global Pharmacovigilance Regulations
Company SOPs
Client and Regulatory Requirements
Maintain audit-ready documentation and records.
Documentation & Quality Management
Maintain accurate pharmacovigilance records and documentation.
Participate in quality checks and internal reviews.
Support process improvement initiatives within the pharmacovigilance function.
Ensure confidentiality of patient and safety-related information.
Cross-Functional Collaboration
Collaborate with:
Drug Safety Teams
Medical Reviewers
Regulatory Affairs Teams
Quality Assurance Teams
Support timely completion of pharmacovigilance deliverables.
Required Qualifications
Education
Bachelor of Dental Surgery (BDS) – Mandatory
Fresh graduates are encouraged to apply.
Experience
Freshers (0–1 Year) eligible.
Internship, training, or certification in Pharmacovigilance will be an added advantage.
Uttar Pradesh :
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