Pharmacovigilance Associate
Centric Edu · Hyderabad · onsite · Posted 47d ago
₹4.0L - ₹6.5L PA0–3 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
Role & responsibilities
- Perform Individual Case Safety Report (ICSR) processing, including case intake, data entry, validation, and follow-up.
- Review and assess adverse event reports from clinical trials, spontaneous sources, literature, and other safety databases.
- Perform case coding using MedDRA and WHO Drug/appropriate coding dictionaries.
- Conduct seriousness, expectedness, and causality assessments as per applicable procedures and guidelines.
- Prepare and submit safety reports within defined regulatory timelines.
- Perform duplicate checks, quality review, and data reconciliation to ensure accuracy and completeness.
- Support follow-up activities for missing or incomplete safety information.
- Maintain accurate documentation and comply with SOPs, GVP guidelines, and regulatory requirements.
- Assist with aggregate safety reporting, signal detection, and safety data analysis as required.
- Collaborate with Clinical, Regulatory Affairs, Medical Writing, and other cross-functional teams.
- Ensure compliance with applicable global pharmacovigilance regulations and company quality standards.
Preferred candidate profile
- Bachelors or Masters degree in Pharmacy, Life Sciences, Medicine, Biotechnology, Nursing, or a related field.
- 03 years of experience in Pharmacovigilance/Drug Safety is preferred; freshers with relevant PV training may also be considered.
- Good understanding of Pharmacovigilance principles, ICSR processing, adverse event reporting, and safety databases.
- Knowledge of MedDRA coding and case processing workflows is an advantage.
- Familiarity with GVP guidelines, ICH guidelines, and regulatory reporting requirements.
- Experience or training in Argus Safety, Medidata Rave, or other pharmacovigilance databases is preferred.
- Strong attention to detail and ability to work accurately with safety data.
- Good written and verbal communication skills.
- Ability to manage multiple cases and meet strict regulatory timelines.
- Good analytical, documentation, and problem-solving skills.
- Willingness to work in a team-oriented and process-driven environment.
You can share your updated Cv in whatsapp to HR Shruti +[phone removed] or HR Riya +[phone removed]
Sourced from naukri
Skills
Healthcare Domainpharmacovigilanceclinical researchClinicalDrug safetyCase ProcessingPharmacyMedicalPharmaceuticalLife Sciences