Veeda Lifesciences Hiring Pharmacovigilance Officer (2 to 3yr) – Apply Now

Veeda Lifesciences Hiring Pharmacovigilance Officer (2 to 3yr) – Apply Now

Veeda Lifesciences, a globally recognized clinical research organization, is currently hiring Pharmacovigilance Officers for its expanding drug safety operations. This is an excellent opportunity for professionals with experience in pharmacovigilance, drug safety, and regulatory compliance to build a rewarding career with a reputed organization in the life sciences domain.

If you are searching for a Pharmacovigilance Officer job, Drug Safety Associate role, or PV career opportunity, this detailed article covers everything you need to know — job role, responsibilities, qualifications, experience, and how to apply.


🏢 About Veeda Lifesciences

Veeda Lifesciences is a leading global CRO offering end-to-end clinical research solutions, including clinical trials, bioavailability studies, pharmacovigilance, regulatory services, and data management.

With a strong global footprint and adherence to international regulatory standards such as ICH, EMA, and FDA, Veeda Lifesciences provides an excellent platform for professionals seeking long-term growth in pharmacovigilance and clinical research.

🌐 Official Website: https://www.veedalifesciences.com


📌 Job Title: Pharmacovigilance Officer

Veeda Lifesciences is hiring Pharmacovigilance Officers to support safety surveillance, regulatory compliance, and case processing activities across clinical studies.


🧪 Key Responsibilities

🔹 Project Monitoring & Management

  • Support departmental coordination using project management tools

  • Prepare study safety documentation including SAE reporting forms

  • Develop training materials for investigator meetings and safety trainings

  • Provide progress updates and study documentation to PV Safety Managers and clients


🔹 Pharmacovigilance Operations

  • Process Serious Adverse Events (SAEs) in compliance with protocols and SOPs

  • Maintain and update internal safety databases

  • Follow up on safety queries with investigative sites

  • Prepare case narratives with high documentation accuracy

  • Submit ICSRs to Ethics Committees, Investigators, and Marketing Authorization Holders

  • Prepare 6-Month SUSAR Line Listings

  • Assist in DSUR (Development Safety Update Report) preparation and submission

  • Support MedDRA coding in coordination with Data Management teams


⚙️ Technical & Functional Competencies

Candidates applying for the Pharmacovigilance Officer role should possess:

  • Strong knowledge of Pharmacovigilance & Drug Safety processes

  • Experience in SAE / ICSR processing

  • Familiarity with MedDRA coding

  • Knowledge of ICH, EMA, and FDA guidelines

  • Proficiency in Microsoft Office & safety databases

  • Strong attention to detail and documentation accuracy


🎓 Educational Qualification

✅ Master’s degree in:

  • Life Sciences

  • Pharmacy

  • Biotechnology

  • Nursing

  • Medical-related fields


🧠 Experience Required

  • 2 to 3 years of experience in Pharmacovigilance / Drug Safety

  • Prior experience in SAE processing and regulatory submissions preferred


📩 How to Apply

Interested candidates can send their updated CV to:

📧 [email protected]

📌 Subject Line Suggestion:
Application for Pharmacovigilance Officer – [Your Name]


🌟 Why Join Veeda Lifesciences?

✔ Reputed global CRO
✔ Exposure to international clinical trials
✔ Strong pharmacovigilance training culture
✔ Growth-oriented work environment
✔ Compliance with global regulatory standards
✔ Excellent career advancement opportunities


📌 Important Notes

  • Only candidates with relevant pharmacovigilance experience should apply

  • Ensure your resume highlights SAE, ICSR, DSUR, and MedDRA experience

  • Early applications are encouraged


Conclusion

The Pharmacovigilance Officer role at Veeda Lifesciences is an excellent opportunity for professionals seeking growth in drug safety and regulatory compliance. With exposure to global studies, strong learning opportunities, and a collaborative environment, this role offers long-term career development in the clinical research industry.

If you meet the eligibility criteria and have experience in pharmacovigilance operations, don’t miss this opportunity — apply today and take the next step in your professional journey.

Pharmacovigilance Officer

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