Lambda Hiring Fresher for PV-ICSR Officer Role: PV Jobs 2026
Lambda Therapeutic Research Ltd., a globally recognized Contract Research Organization (CRO), is hiring Officer – ICSR professionals for its Pharmacovigilance team. This is an excellent opportunity for fresh graduates in Pharmacy or Life Sciences who are looking to begin their career in drug safety, ICSR case processing, and global pharmacovigilance operations.
In this role, you will work on Individual Case Safety Reports (ICSRs), perform MedDRA coding, drug coding, duplicate checks, narrative writing, and ensure all safety cases comply with international pharmacovigilance guidelines. With Lambda’s strong global footprint — spanning India, USA, Canada, UK, Spain, and Poland — you will gain exposure to worldwide safety standards and end‑to‑end clinical research processes.
Job Overview
- Position: PV-ICSR Officer
- Department: Pharmacovigilance
- Location: Ahmedabad, India
- Experience: 0 to 1 Years
- Qualification: B.Pharm, M.Pharm,M.Sc
- Job Type: Full-Time
Key Responsibilities – Pharmacovigilance ICSR Oficer
- ICSR Case Processing: Perform end‑to‑end pharmacovigilance case processing, including duplicate checks, validation, data entry, drug coding, MedDRA coding, listedness, causality assessment, expediting assessment, and narrative writing, following SOPs, Work Instructions, and regulatory guidelines.
- Documentation & Quality Compliance: Prepare, review, and update SOPs, WIs, templates, and training materials. Ensure all safety activities meet local and global PV quality standards, regulatory timelines, and documentation requirements.
- Safety Communication: Immediately communicate urgent safety issues to the Line Manager and QPPV, while maintaining professional communication and accurate documentation for all internal/external correspondence.
- Training & Mentoring: Conduct training sessions for new joiners and support team members. Mentor less experienced colleagues to help them perform their responsibilities effectively.
- Team Collaboration & Escalation: Work closely with the ICSR Team Leader to escalate challenges. Assist the Group Leader in achieving 100% regulatory compliance for timely case processing.
- Client & Regulatory Interaction: Provide pharmacovigilance guidance to clients and colleagues when needed. Communicate with clients and regulatory authorities as required.
- Continuous Improvement: Stay updated on evolving regulatory intelligence and implement changes accordingly. Assist in developing SOPs for Lambda’s PV department and client projects.
- Additional Responsibilities: Perform any other tasks assigned by the Line Manager to meet operational and business needs.
Required Skills & Qualifications
- Educational Background:
A student wih B.Pharm, M. Pharm degree - Medical & Scientific Knowledge:
Strong understanding of medical terminology, pharmacology, anatomy, and physiology, essential for accurate interpretation and coding of clinical trial data. - Attention to Detail & Problem-Solving:
Excellent attention to detail with the ability to work independently, apply critical thinking, and proactively resolve coding or data discrepancies. - SOP & Process Knowledge:
Familiarity with standard operating procedures (SOPs), work instructions, and the ability to apply them consistently in daily tasks. - Communication & Leadership:
Strong written and spoken English communication skills, along with organizational abilities and leadership qualities suitable for cross-functional collaboration.
Why Join ACCENTURE?
Work With a Global CRO
Lambda is a well‑established global Contract Research Organization operating across India, USA, Canada, UK, Spain, and Poland, giving you exposure to international pharmacovigilance standards and global clients.
Strong Learning & Career Growth
As an Officer – ICSR, you gain hands‑on experience with end‑to‑end case processing, MedDRA coding, safety regulations, compliance workflows, and real‑world PV operations — building a solid foundation for long‑term career growth.
Structured Training & Mentorship
Lambda provides continuous training, guidance from experienced leaders, and opportunities to take on responsibilities like SOP development, compliance support, and mentoring junior team members.
High‑Impact Work in Drug Safety
Your work directly contributes to patient safety by supporting accurate case reporting, regulatory compliance, and global safety standards — making the role meaningful and impactful.
How to Apply
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer
This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.
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FAQ
1. Is this role suitable for freshers?
Yes. This position is ideal for fresh graduates in Pharmacy or Life Sciences who want to begin a career in pharmacovigilance and ICSR case processing.
2. What does an Officer – ICSR do at Lambda?
You will work on end‑to‑end ICSR case processing, including duplicate checks, MedDRA coding, drug coding, narrative writing, causality assessment, and ensuring regulatory‑compliant case submissions.
3. Do I need prior pharmacovigilance experience?
Not mandatory. Freshers with strong life sciences knowledge and interest in PV are encouraged to apply. Training and mentorship are provided.
4. What skills are required for this role?
- Knowledge of life sciences
- Attention to detail
- Good communication skills
- Ability to follow SOPs and guidelines
- Basic understanding of drug safety terms (preferred, not mandatory)
5. Will I work with global teams or clients?
Yes. Lambda works with clients across India, USA, Canada, UK, Spain, and Poland, giving you exposure to global PV expectations and processes.
