"Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers | Pharma Duniya"

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"Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers | Pharma Duniya." (Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers) Introduction If you are a fresher or early-career professional aiming to build a strong career in Medical Device Regulatory Affairs and Quality Assurance , this opportunity can be a perfect starting point. ELEXES Medical Consulting Pvt. Ltd. has announced hiring for the position of Project Associate I – Regulatory Affairs & Quality Assurance (RA/QA) . This role is specially designed for fresh graduates and candidates with up to 6 months of experience who want hands-on exposure to global medical device regulations , including US FDA, EU MDR, CDSCO, Health Canada , along with ISO 13485 quality systems . The position offers real project experience under expert mentorship, making it ideal for long-term growth in the medical device regulatory domain. About The Company – ELEXES Medical Consulting Pvt. Ltd. EL...

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"Syneos Health Hiring Pharmacovigilance Trainee | 2025 Pass-Outs Eligible | Apply Now"

"Syneos Health Hiring Safety & Pharmacovigilance Trainees (2025 Pass-Outs) – Apply Now"


Syneos Health, one of the world’s leading Contract Research Organizations (CROs), is inviting applications for the role of Safety & Pharmacovigilance Trainee. This opportunity is exclusively for 2025 pass-outs from M.Pharm, Pharm.D, BHMS, BDS, M.Sc (with B.Pharm), or Ph.D (Pharmacy).

This contractual trainee position offers hands-on exposure to drug safety, pharmacovigilance operations, and regulatory compliance, making it an excellent launchpad for fresh graduates looking to build a career in the pharmaceutical industry.

Key Responsibilities:-

As a Safety & Pharmacovigilance Trainee, selected candidates will:

  • Monitor, record, and route incoming safety information.
  • Assist in ICSR documentation, tracking, and patient data redaction.
  • Enter and validate data in the safety database.
  • Support literature screening, drug coding, and MedDRA dictionary updates.
  • Work on query resolution, workflow reconciliation, and safety report submissions.
  • Assist in narrative writing, event coding, and duplicate case management.
  • Ensure compliance with ICH-GCP, GVP guidelines, SOPs, and global pharmacovigilance standards.
  • Participate in audits and contribute to accurate documentation in TMF/PVSMF systems.

Eligibility & Qualifications:-

Education (Only 2025 Pass-Outs Eligible):

  • M.Pharm / Pharm.D
  • M.Sc (with B.Pharm)
  • BHMS / BDS
  • Ph.D (Pharmacy)

Core Skills Required:

  • Keen interest in pharmacovigilance and drug safety
  • Excellent verbal and written communication skills
  • Good knowledge of MS Office & Outlook
  • Strong multitasking and organizational skills
  • Attention to detail and accuracy

Preferred Skills:

  • Familiarity with pharmacology, safety databases, and medical terminology
  • Experience with collaboration tools (e.g., Visio, Team Share)

Why Join Syneos Health?

  • Work with a global CRO trusted by 94% of FDA-approved drugs in the last 5 years.
  • Gain access to structured pharmacovigilance training and mentorship programs.
  • Hands-on exposure to drug safety processes and regulatory practices.
  • Collaborative and inclusive work culture.
  • 1-year contractual role with possible extension based on performance.

Job Location & Type:-

  • Location: Gurugram, India
  • Type: Contractual (1 Year, Renewable)
  • Organization: Syneos Health

Salary / Stipend:-

  • Estimated stipend: ₹25,000 – ₹40,000 per month (approx.)
  • Based on industry standards for PV trainee roles

How to Apply:-

Interested candidates can apply online through the official link below:

👉 Apply Here – Syneos Health Safety & Pharmacovigilance Trainee Jobs 2025

✨ This is a golden chance for fresh pharmacy and life science graduates to begin their journey in pharmacovigilance and clinical research with a globally recognized CRO.

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