Job Title: Officer – ICSR
Req ID: 1432
Date: January 10, 2026
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range (INR): 300,000 – 500,000
Lambda Therapeutic Research Ltd. is a leading global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With strategically located facilities in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland), we provide comprehensive end-to-end clinical research services to innovators, biotech firms, and pharmaceutical companies worldwide.
Our commitment to quality, regulatory compliance, and scientific excellence enables us to deliver reliable pharmacovigilance and clinical trial solutions across diverse therapeutic areas.
We are seeking a dedicated ICSR Officer to join our Pharmacovigilance team in Ahmedabad. This role involves accurate case processing, regulatory compliance, and collaboration with global stakeholders to ensure high-quality safety reporting. The ideal candidate will have a strong foundation in life sciences or pharmacy and be eager to contribute to a fast-paced, dynamic pharmacovigilance environment.
Process pharmacovigilance cases, including duplicate search, validation, and accurate data entry.
Perform drug coding, MedDRA coding, listedness, causality assessment, expedited reporting, and narrative writing in compliance with SOPs, work instructions, and global regulatory guidelines.
Prepare, review, and maintain SOPs, templates, training documents, and operational guides.
Report urgent safety concerns promptly to the Line Manager and QPPV.
Maintain accurate internal and external correspondence with professional communication standards.
Ensure adherence to quality standards, procedures, and global/local PV regulatory requirements.
Conduct training for new joiners and support ongoing team development.
Collaborate with the ICSR Team Leader for escalation of complex cases.
Support the Group Leader in achieving 100% compliance with regulatory timelines.
Provide pharmacovigilance guidance to colleagues and clients as needed.
Mentor junior team members to enhance their skills and performance.
Stay updated on global regulatory intelligence and implement process improvements.
Communicate with clients and regulatory authorities when required.
Perform additional tasks as assigned by the Line Manager to support business needs.
Freshers are welcome to apply; prior internship or exposure to pharmacovigilance is a plus.
Bachelor’s degree in Life Sciences, Pharmacy, or a related field.
Opportunity to work in a global CRO with exposure to international pharmacovigilance standards.
Hands-on experience in ICSR processing and regulatory compliance.
Career growth through mentorship, training, and exposure to diverse therapeutic areas.
Apply Now at The Pharma Daily to join a team committed to advancing pharmacovigilance excellence worldwide.
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