"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs"

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"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs" (Syneos Health Hiring Safety & PV Coordinator in Hyderabad) Introduction Candidates looking to build a strong and long-term career in Pharmacovigilance (PV) and Drug Safety have an excellent opportunity at Syneos Health , a globally recognized biopharmaceutical solutions organization. Syneos Health is currently hiring for the position of Safety & PV Coordinator at its Hyderabad office . This is a full-time, office-based role , ideal for professionals who have experience or exposure in pharmacovigilance submissions, safety reporting, regulatory compliance, and clinical research processes . Working with a global organization like Syneos Health provides exposure to international safety regulations, cross-functional teams, and structured career growth . About The Company – Syneos Health Syneos Health® is a fully integrated biopharmaceutical solutions organization that supports pha...

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"Work-from-Office Opportunity: Vizen Life Sciences Hiring Pharmacovigilance Professionals in Hyderabad"

"Drug Safety Associate Jobs in Hyderabad at Vizen Life Sciences | Pharmacovigilance Careers 2025"

(Vizen Life Sciences Hiring)

Are you passionate about ensuring drug safety and patient well-being? Vizen Life Sciences, a reputed name in pharmaceutical services, is hiring for Drug Safety Associate (DSA) and Pharmacovigilance (PV) professional roles in Hyderabad. This work-from-office opportunity is ideal for individuals with 1–3 years of experience in post-marketing surveillance, case processing, and ARGUS Safety Database operations.

Join a collaborative team dedicated to maintaining high safety standards and regulatory compliance in global drug safety management.

Job Overview: Drug Safety Associate / Pharmacovigilance Professional:-

At Vizen Life Sciences, the selected candidates will play a crucial role in handling pharmacovigilance case processing and maintaining patient safety data. This includes managing adverse event reports, ensuring data accuracy, and supporting regulatory submissions as per global PV guidelines.

Key Responsibilities:-

  • Process and review adverse event (AE) cases from spontaneous and post-marketing sources.
  • Perform data entry, case assessment, and narrative writing using the ARGUS Safety Database.
  • Ensure compliance with global pharmacovigilance regulations (FDA, EMA, ICH, WHO).
  • Support quality checks and audit readiness for PV documentation.
  • Collaborate with cross-functional teams for case tracking and timely submissions.
  • Maintain confidentiality and accuracy in drug safety reporting activities.

Eligibility Criteria:-

  • Qualification: B.Pharm, M.Pharm, or Life Sciences graduate/postgraduate.
  • Experience: 1–3 years in pharmacovigilance/drug safety operations.
  • Tools: Practical experience with the ARGUS Safety Database is a must.
  • Skills: Strong communication, analytical ability, and documentation accuracy.
  • Work Mode: 100% on-site (work from office) – Gachibowli, Hyderabad.

Why Join Vizen Life Sciences?

  • Hands-on experience with global PV case management systems.
  • Exposure to international regulatory standards and drug safety workflows.
  • Opportunity to grow in one of the most in-demand pharma domains – pharmacovigilance.
  • Competitive salary range of ₹4–6 LPA (based on experience).
  • Supportive and knowledge-driven work environment.

How to Apply:-

Interested professionals meeting the eligibility criteria can send their updated resume to:

Email: plotti@vizenlifesciences.com
Contact: Praveen Kumar (General Manager – HR) – +91 8008102515

Location: Gachibowli, Hyderabad
Experience Required: 1–3 years

FAQs:-

1. Who can apply for Vizen Life Sciences pharmacovigilance jobs?
Candidates with 1–3 years of experience in drug safety, case processing, or ARGUS operations are eligible.

2. Is this a remote or office-based job?
This is a 100% work-from-office position located in Hyderabad, Telangana.

3. What tools are used for case management?
Candidates should be proficient in the ARGUS Safety Database for handling PV and AE cases.

Conclusion:-

If you’re a motivated professional with a background in pharmacovigilance and drug safety, this opportunity at Vizen Life Sciences can accelerate your pharma career. Apply today and become part of a team that contributes to global patient safety and regulatory excellence.

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