Are you a qualified pharmacy professional looking to advance your career in the field of pharmacovigilance? Sri Venkateswara Institute of Medical Sciences (SVIMS) in Tirupati, Andhra Pradesh, is hiring for the position of Pharmacovigilance Associate on a contract basis. This is a fantastic opportunity for aspiring professionals to work with a prestigious institute, contributing to drug safety initiatives under the Pharmacovigilance Programme of India (PvPI).
About the Indian Pharmacopoeia Commission (IPC)
The Indian Pharmacopoeia Commission (IPC) operates under the Ministry of Health and Family Welfare, Government of India. Its primary role involves regularly updating the Indian Pharmacopoeia, which includes the publication of new editions and addenda, as well as the creation and distribution of reference substances. IPC also functions as the National Coordination Centre for the Pharmacovigilance Programme of India. By joining SVIMS, you will play an integral role in these crucial tasks.
Position Details
Job Title: Pharmacovigilance Associate (01 Position)
Department: Pharmacology, SVIMS, Sri Padmavathi Medical College for Women, Tirupati
Job Type: Contract Basis
Salary: ₹26,250 per month
Essential Qualifications
Candidates interested in applying for the Pharmacovigilance Associate position must meet the following qualifications:
- Master’s Degree in:
- Pharmacy
- Clinical Pharmacology
- Pharmacy Practice
- Clinical Research
- Bachelor in Pharmacy (Pharm. D.), MBBS, or BDS from a recognized university or institution.
Desirable Qualifications
- A minimum of one year of experience in drug safety or pharmacovigilance will be considered an advantage.
Age Limit
Candidates applying for this position must not exceed the age of 28 years.
Job Responsibilities
As a Pharmacovigilance Associate at SVIMS, your responsibilities will include:
- Collection of Adverse Drug Reaction (ADR) Reports – Gathering and documenting information on any adverse effects observed with drug usage.
- Processing of Individual Case Safety Reports (ICSRs) – Efficient management and processing of ICSR data using VigiFlow software.
- Quality Review – Conducting clinical and statistical reviews of ICSRs while ensuring data integrity in the Drug Safety database.
- Other Responsibilities – Performing any additional tasks assigned by the competent authority as needed.
Why Choose SVIMS?
Working at SVIMS not only provides an excellent platform for career growth but also an opportunity to contribute to critical health initiatives in the country. The pharmacovigilance role at SVIMS is a gateway to gaining valuable experience, networking with industry professionals, and enhancing your expertise in drug safety.
By engaging with the Pharmacovigilance Programme of India, you will be at the forefront of ensuring the safety and efficacy of medications, thus improving patient health outcomes across the nation.
How to Apply
Interested candidates should download the application format from the SVIMS website: http://svimstpt.ap.nic.in/. Applications must be accompanied by attested copies of relevant documents and submitted on or before 12th February 2025.
Completed applications should be scanned and sent in PDF format via email to svimspharmacovigilance@gmail.com.
