"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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"ProPharma Hiring Pharmacovigilance Safety Scientist in India – Apply Now"

"ProPharma Hiring Pharmacovigilance Safety Scientist in India – Apply Now"



(ProPharma Hiring Pharmacovigilance)



Are you passionate about drug safety and pharmacovigilance? ProPharma, a trusted global leader in regulatory sciences, clinical research, and drug safety, is inviting applications for the Pharmacovigilance Safety Scientist role in India. This position offers an excellent opportunity to work on global projects and contribute to improving patient safety worldwide.


Key Responsibilities:-

As a Pharmacovigilance Safety Scientist at ProPharma, you will be responsible for:

  • Authoring aggregate safety reports such as PSURs, PBRERs, PADERs, Annual Reports, ACO, and DSUR.
  • Developing and maintaining Risk Management Plans (RMPs).
  • Preparing Signal Management Reports and conducting literature searches.
  • Reconciling process trackers and validating extracted data.
  • Generating and reviewing line listings from safety databases.
  • Supporting ad-hoc pharmacovigilance activities as per project requirements.
  • Ensuring all deliverables meet ICH-GCP, FDA, EMA, and global PV regulations.
  • Contributing to SOPs, deviations, and CAPA activities.
  • Analyzing large volumes of safety data with precision and accuracy.


Required Qualifications & Skills:-

  • Education: Bachelor’s/Master’s in Pharmacy, Nursing, Life Sciences, or related health sciences.
  • Experience: Minimum 2+ years in pharmacovigilance, with expertise in medical writing, signal detection, or literature review.
  • Strong understanding of global PV regulations.
  • Excellent communication, writing, and analytical skills.
  • Proficiency in MS Office tools and PV database applications.
  • Ability to work in a matrix and multicultural environment.


Why Join ProPharma?

  • Be part of a global leader in pharmacovigilance and regulatory sciences.
  • Contribute to patient safety and global healthcare improvement.
  • Opportunity to work with a collaborative, diverse, and inclusive team.
  • Strong career growth in drug safety, PV, and medical writing.


How to Apply:-

Interested candidates can apply directly through the official link below:

πŸ‘‰ Apply Here – Pharmacovigilance Safety Scientist at ProPharma India


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