Associate / Senior Associate Case Processing

Primary Responsibilities:

• Perform Intake/Triage, Data Entry, and Quality Review for individual case safety reports from a variety of sources, including spontaneous, literature, regulatory, and clinical trial cases.
• Manage case finalization and distribution, ensuring timely and accurate submission.
• Raise follow-up queries as needed and maintain complete documentation in the safety database.

Candidate Profile: 

• Bachelor’s or Master’s in Pharmacy / Life Sciences or above and in alignment with project / business team requirements.
• Must have hands-on experience with MS office applications (Outlook, Excel, Word, Power Point etc.). 
• Must possess knowledge of ICH-GCP, relevant GVP module, 21 CFR guidelines and other regulatory requirements.
• Training and mentoring skills(ICSR, Safety database etc.).
• Fresh graduates are welcome to apply.