"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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"Clinical Trial Assistant (CTA) Internship at Eccentric Clinical Research, Gandhinagar – Apply Now" ✅

"Clinical Trial Assistant (CTA) Interns Jobs at Eccentric Clinical Research – Gandhinagar, Gujarat"


Eccentric Clinical Research, a rapidly growing Contract Research Organization (CRO) in India, is inviting applications for Clinical Trial Assistant (CTA) Interns at its Gandhinagar, Gujarat facility. This is an excellent opportunity for fresh graduates in Life Sciences, B.Pharm, or M.Pharm who are passionate about building a career in clinical trials, GCP compliance, and regulatory affairs.

Working as a CTA Intern at Eccentric Clinical Research will give you practical exposure to clinical operations, documentation, and regulatory submissions, along with mentorship from experienced professionals.


Key Responsibilities – CTA Intern:-

As a Clinical Trial Assistant Intern, you will:

  • Maintain and update the Trial Master File (TMF/eTMF).
  • Assist with regulatory and ethics committee submissions and documentation.
  • Handle version control, filing, and archival of study documents.
  • Support CRAs and Project Managers during study setup, initiation, monitoring, and close-out activities.
  • Track clinical trial progress using dashboards, trackers, and reports.
  • Coordinate with sites, investigators, and vendors for trial-related activities.
  • Manage distribution and tracking of study supplies and shipments.
  • Ensure compliance with ICH-GCP guidelines, SOPs, and regulatory requirements.
  • Contribute to safety reporting, SAE tracking, audit readiness, and process improvements.

Eligibility Criteria:-

  • Qualification: B.Sc / M.Sc (Life Sciences), B.Pharm, or M.Pharm.
  • Experience: 0–2 years (freshers with internships are encouraged).
  • Skills Required:
    • Knowledge of clinical trial processes, ICH-GCP, and regulatory guidelines.
    • Strong organizational & documentation skills.
    • Proficiency in MS Office (Word, Excel, PowerPoint) and trial management tools.
    • Ability to multitask and work in fast-paced environments.

Why Join Eccentric Clinical Research?

✅ Hands-on experience in clinical operations & trial management.
✅ Training & mentorship from senior CRAs and project managers.
✅ Exposure to regulatory submissions and eTMF systems.
✅ Growth opportunities into CRA and Project Management roles.
✅ Supportive and collaborative work culture.


Job Location:-

  • Gandhinagar, Gujarat, India

Salary Package:-

  • INR 2,00,000 – 3,60,000 per annum (depending on qualifications and performance).

How to Apply?

Interested candidates can apply by sending their updated CV to:
📧 hr@eccentriccr.com

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