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

Image
"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...

Pharma Duniya is a trusted platform providing the latest pharma job updates, walk-in interviews, clinical research openings, and pharmacy career guidance. All job information is collected from official company websites and public sources. We do not charge any fees and are not official recruiters.

"Sanofi Hiring Clinical Trial Support Associate in Hyderabad – Apply Before February 13, 2026"

"Sanofi Hiring Clinical Trial Support Associate in Hyderabad – Apply Before February 13, 2026"




(Sanofi Hiring Clinical Trial Support Associate in Hyderabad)




Sanofi, one of the world’s leading biopharmaceutical companies, has announced a new hiring opportunity for the position of Clinical Trial Support Associate (CTSA) at its Hyderabad location. This role is a great opportunity for life science graduates who want to build a long-term career in clinical research, clinical trial operations, and regulatory compliance.

With increasing global focus on innovative medicines, vaccines, and rare disease treatments, Sanofi continues to expand its clinical research operations in India. The CTSA role plays a critical part in ensuring smooth execution and compliance of global clinical trials.


Introduction

Clinical research careers are among the most stable and high-growth options for pharmacy and life science graduates. Roles like Clinical Trial Support Associate provide exposure to global regulatory standards, trial documentation, and cross-functional collaboration.

Sanofi’s Clinical Trial Support Associate job in Hyderabad is ideal for candidates who want hands-on experience in clinical trial coordination while working with one of the most respected pharmaceutical companies in the world.


About The Company – Sanofi

Sanofi is a global biopharmaceutical company headquartered in Paris, France, with a strong presence in more than 100 countries. The company focuses on developing innovative healthcare solutions in areas such as vaccines, rare diseases, chronic conditions, immunology, and specialty care.

Company Overview:

  • Company Name: Sanofi

  • Founded: 1973

  • Headquarters: Paris, France

  • Global Employees: 90,000+

  • Presence in India: Hyderabad, Mumbai, Goa, and other locations

Sanofi is widely known for its ethical practices, innovation-driven culture, and commitment to patient safety and diversity.


Job Overview Summary

Sanofi is hiring for the Clinical Trial Support Associate (CTSA) role to support clinical trial operations and documentation activities. The position involves coordination with clinical trial sites, internal teams, and vendors while ensuring compliance with GCP, ICH, FDA, and EMA guidelines.

This role offers strong learning opportunities for candidates aiming to grow into Clinical Research Associate (CRA), Clinical Operations Manager, or Regulatory roles.


Vacancy Details (Official)

  • Job Title: Clinical Trial Support Associate (CTSA)

  • Company: Sanofi

  • Job Location: Hyderabad

  • Department: R&D / Clinical Operations

  • Last Date to Apply: February 13, 2026

  • Job Type: Full-Time


Job Role & Responsibility Explanation

As a Clinical Trial Support Associate at Sanofi, the selected candidate will support various operational and documentation activities across ongoing clinical trials.

The role includes managing study-related communications, maintaining trial documentation, coordinating with internal and external stakeholders, and supporting audit readiness. CTSA professionals ensure that all trial activities are conducted in accordance with global regulatory requirements and internal SOPs.

This position is essential for maintaining trial quality, compliance, and timely execution.


Key Responsibilities (Explained)

The CTSA will be responsible for distributing study-related documents such as protocol amendments, investigator brochures, and newsletters to trial sites. Maintaining logs for informed consent forms, training records, and patient data reports is a core responsibility.

The role also involves maintaining the Trial Master File (TMF), managing SharePoint archiving, and supporting audit and inspection readiness, including Pre-Approval Inspections (PAIs).

Additionally, the CTSA will support financial and vendor coordination by managing invoices, purchase orders, and payment tracking, while also handling Clinical Trial Management Systems (CTMS) setup, reporting, and compliance monitoring.


Eligibility Criteria (Official)

Educational Qualification:

  • Bachelor’s degree in Life Sciences, Healthcare Administration, or equivalent

Experience:

  • Prior exposure to clinical research operations preferred

  • Knowledge of GCP and ICH guidelines is an advantage


Skills Required 

Candidates should have strong communication skills, especially in English, as the role involves global collaboration. A good understanding of clinical trial documentation, compliance processes, and clinical systems is essential.

The ability to multitask, manage deadlines, and work in a fast-paced research environment is highly valued. Attention to detail and problem-solving skills are critical for success in this role.


Salary Estimate

While Sanofi has not officially disclosed the salary, Clinical Trial Support Associates in global pharma companies typically earn ₹6 LPA to ₹10 LPA in India, depending on experience, skills, and internal compensation structure.


Employee Benefits at Sanofi

Sanofi offers an attractive benefits package, including competitive salary, performance-based bonuses, health and wellness programs, and continuous learning opportunities. Employees also benefit from global mobility options and a respectful, inclusive work culture.


Interview Details (Official)

  • Interview Mode: Online / Virtual

  • Selection Process: Resume screening followed by technical and HR interviews

Shortlisted candidates will be contacted through the official Sanofi recruitment process.


Required Documents

Applicants should keep the following documents ready:

  • Updated resume

  • Educational certificates

  • Government ID proof

  • Experience letters (if applicable)


How to Apply (Official Method)

Interested candidates must apply online through the official Sanofi careers portal.

Apply Link:
https://sanofi.wd3.myworkdayjobs.com/en-US/SanofiCareers/job/Hyderabad/R-D-Clinical-Trial-Support-Associate_R2814748

Last Date to Apply: February 13, 2026


FAQs – Sanofi Clinical Trial Support Associate Job

Q1. Is this job suitable for freshers?
Candidates with basic exposure to clinical research are preferred, but motivated freshers with relevant knowledge may apply.

Q2. What is the work location?
The job location is Hyderabad.

Q3. Is this a permanent position?
Yes, this is a full-time permanent role.

Q4. What career growth is possible after CTSA?
Candidates can grow into CRA, Clinical Operations Manager, or Regulatory roles.

Q5. Is GCP knowledge mandatory?
GCP knowledge is highly preferred and beneficial for selection.


Final Conclusion

The Clinical Trial Support Associate job at Sanofi is a valuable opportunity for life science graduates who want to enter the global clinical research industry. With strong exposure to regulatory standards, documentation, and trial operations, this role can serve as a solid foundation for a long-term career in pharma R&D.

Candidates are advised to apply before the deadline and prepare well to make the most of this opportunity.

Note: Pharma Duniya does not charge any money for job information.
Candidates are advised to verify details from the official company website.


πŸ“„ Resume Getting Rejected Again & Again?

Kya aapka resume bar-bar reject ho raha hai?
Kya interview calls nahi aa rahi, chahe qualification aur skills ho?

Aaj ke competitive pharma job market me 90% resumes ATS (Applicant Tracking System) ke stage par hi reject ho jaate hain, kyunki:

  • Resume outdated format me hota hai

  • Pharma-specific keywords missing hote hain

  • HR-friendly & role-specific structure nahi hota

  • QA, QC, PV, Clinical Research roles ke hisaab se customisation nahi hoti

✅ Get Your Pharma Resume Professionally Written (Trusted Solution)

Pharma Duniya lekar aaya hai Professional Pharma Resume Writing Service, jo specially pharma & life science candidates ke liye design ki gayi hai.

πŸ”Ή Is service me aapko milta hai:

  • ✔ Fresher & Experienced candidates ke liye resume

  • ✔ 100% ATS-friendly format

  • ✔ HR-approved & industry-standard layout

  • ✔ QA, QC, IPQA, Pharmacovigilance, Clinical Research, Regulatory Affairs ke hisaab se customisation

  • ✔ Clear, clean & professional presentation

πŸ”— Check Resume Writing Service:
πŸ‘‰ https://www.pharmaduniya.com/p/professional-pharma-resume-writing.html

πŸ“² WhatsApp support available for quick resume guidance


WhatsAppShare on WhatsApp

Recommended Pharma Career & Job Updates (Must Read)

If you are preparing for pharma job interviews or actively searching for the latest QA, QC, Pharmacovigilance jobs and walk-in interviews, don’t miss these important and student-friendly career resources from Pharma Duniya πŸ‘‡


πŸ“„ "Documents Required for Pharma Interview – Complete Checklist."

Are you confused about which documents are required for pharma interviews? This complete checklist is specially designed for B.Pharm, M.Pharm, Pharm.D & Life Sciences candidates to avoid last-minute mistakes during interviews and walk-ins.

πŸ‘‰ See More:
https://www.pharmaduniya.com/2025/12/documents-required-for-pharma-interview.html


❤️ "Pharma QA Interview Preparation for Freshers (Complete Guide 2026) – Questions, Tips & Career Path."

Pharma QA Interview Preparation for Freshers (Complete Guide) for B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences - Candidates who want to build a career in Quality Assurance (QA).

πŸ‘‰ Apply Here:
https://www.pharmaduniya.com/2026/01/pharma-qa-interview-preparation-for-freshers.html


🎯 "How to Get an Internship or Industrial Training After B.Pharm / M.Pharm / M.Sc"

Planning for industrial training or internship after B.Pharm, M.Pharm, or M.Sc? This complete student guide (2025-26) explains how to apply, where to apply, and how to get selected for pharma industrial training programs.

πŸ‘‰ See Full Guide:
https://www.pharmaduniya.com/2025/10/Industrial%20Training.html


πŸ“’ Stay Updated with Latest Pharma Jobs & Walk-In Interviews

If you want daily verified updates on QA, QC, Pharmacovigilance, Clinical Research, and Pharma Walk-In Interviews, join Pharma Duniya’s official channels and never miss an opportunity.

✅ Join our WhatsApp Group
✅ Join our Telegram Channel

πŸ“Œ Get verified pharma job alerts, interview tips, resume guidance, and student career support directly on your phone.

🌐 Visit daily: www.pharmaduniya.com 

Popular posts from this blog

"Freshers Guide for Pharma Walk-In Interviews 2025-26 | QA, QC & Production Jobs"

"How to Start a Career in Pharmacovigilance as a Fresher – Complete 2025 Guide"

“Fortrea Hiring Assistant I PSS in Pune – Pharmacovigilance & Drug Safety Careers”