We are seeking experienced Drug Safety Associates (Pharmacovigilance Professionals) to join our team. If you have a strong background in PV case processing, ICSR management, and regulatory compliance, this is an excellent opportunity for you!

Key Responsibilities:

• Processing and assessing Individual Case Safety Reports (ICSRs)
• Ensuring compliance with global pharmacovigilance regulations (FDA, EMA, ICH-GCP)
• Data entry and quality review of adverse event reports
• Literature screening for safety information
• Writing and reviewing safety narratives
• Collaborating with cross-functional teams for risk management

Required Skills & Qualifications:

• 1+ years of experience in Pharmacovigilance (Mandatory)
• Strong knowledge of Argus, Veeva, or other safety databases
• Familiarity with MedDRA and WHO-DD coding
• Excellent communication and analytical skills
• Ability to work independently in a remote setup

About Qinecsa & Pharmabharat

Qinecsa is a leading name in the pharmacovigilance and drug safety domain, providing end-to-end solutions to global pharmaceutical companies.

Pharmabharat.com is a trusted platform for pharma job postings, industry news, and career guidance, helping professionals find the best opportunities in the life sciences sector.

How to Apply?

If you meet the eligibility criteria and are interested in this remote Drug Safety Associate role, please share your updated resume with the subject line:

“Drug Safety Associate – [Your Notice Period]”

Email: Nithin.vijendra@qinecsa.com

🔹 Only shortlisted candidates will be contacted.
🔹 Immediate joiners will be given preference.