"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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"Latest Pharma Jobs medONE Solution Hiring Clinical Research Associate (CRA) in Gurgaon 2026."

"medONE Solution Hiring Clinical Research Associate (CRA) in Gurgaon | Pharma Jobs 2026"



(medONE Solution Hiring Clinical Research Associate in Gurgaon 2026)

Introduction

Pharmaceutical और Clinical Research industry में करियर बनाने वालों के लिए एक शानदार मौका सामने आया है। medONE Solution, जो कि एक COSCO-registered Clinical Research Organization (CRO) है, ने Clinical Research Associate (CRA) पद के लिए भर्ती की घोषणा की है। यह भर्ती Gurgaon (Delhi NCR) लोकेशन के लिए है और यह भूमिका उन Pharmacy और Life Sciences professionals के लिए उपयुक्त है जो clinical monitoring, GCP compliance और regulatory processes में hands-on experience चाहते हैं।

Clinical research jobs India में लगातार demand में हैं और CRA profile को pharma industry की सबसे stable और growth-oriented roles में गिना जाता है। medONE Solution के साथ काम करना candidates को early-phase से लेकर post-marketing studies तक exposure देता है, जिससे long-term career growth के chances बढ़ जाते हैं।


About medONE Solution (Company Introduction)

medONE Solution एक reputed और fast-growing Clinical Research Organization (CRO) है, जो clinical trials के late-phase और post-marketing studies में दशकों का अनुभव रखती है। कंपनी COSCO-registered है और international regulatory standards जैसे ICH-GCP, USFDA, और EMA guidelines का पालन करती है।

  • Company Name: medONE Solution

  • Industry: Clinical Research & Drug Development

  • Company Type: COSCO-registered CRO

  • Headquarters: Gurgaon, Haryana (Delhi NCR), India

  • Established: लगभग 2010 के आसपास

  • Experience: 10+ वर्षों का clinical research experience

  • Employees: 50–200+ professionals (clinical, regulatory & operations team)

medONE Solution ने अब early-phase clinical trials में भी expansion शुरू किया है और इसी expansion के तहत clinical operations team को मजबूत किया जा रहा है।


Job Overview – Clinical Research Associate (CRA)

इस vacancy के तहत selected candidates को Clinical Research Associate (CRA) के रूप में नियुक्त किया जाएगा। CRA की भूमिका clinical trial sites की monitoring, data accuracy सुनिश्चित करने और regulatory compliance बनाए रखने में अहम होती है।

यह एक Full-Time pharma job है और responsibilities candidate के experience level के अनुसार assign की जाएंगी।


Vacancy Details (Official)

  • Position: Clinical Research Associate (CRA)

  • Job Code: MED-CRA-001-2026

  • Location: Gurugram, Haryana (Delhi NCR)

  • Employment Type: Full-Time

  • Organization: medONE Solution


Job Role & Responsibilities (Detailed Explanation)

Clinical Research Associate के रूप में candidate को निम्न responsibilities निभानी होंगी:

  • Clinical trial sites पर regular monitoring visits conduct करना

  • Source Data Verification (SDV) के माध्यम से data accuracy ensure करना

  • Investigator Site File (ISF) और Trial Master File (TMF) को maintain करना

  • Study protocol, SOPs और ICH-GCP guidelines का compliance सुनिश्चित करना

  • Adverse Events (AE) और Serious Adverse Events (SAE) documentation में support देना

  • Investigators, sponsors और internal study teams के साथ coordination करना

  • Regulatory audits और inspections के लिए sites को inspection-ready बनाए रखना

  • Clinical trial documentation की quality और completeness ensure करना

यह भूमिका उन candidates के लिए best है जो clinical research operations में long-term career बनाना चाहते हैं।


Eligibility Criteria (Official)

  • Pharmacy, Life Sciences या related field में Bachelor’s या Master’s degree

  • Clinical research monitoring का hands-on experience

  • ICH-GCP, regulatory requirements और clinical operations का knowledge

  • Multiple clinical trial sites independently manage करने की ability

  • Strong communication और documentation skills

  • Travel करने की willingness


Skills Required 

  • Clinical trial regulations की practical understanding

  • Good communication और professional email writing skills

  • Documentation accuracy और attention to detail

  • Time management और multitasking ability

  • EDC, CTMS और eTMF systems की basic knowledge

  • Team coordination और problem-solving mindset


Salary Estimate 

Expected Salary: ₹4.5 LPA – ₹8 LPA
(Actual salary candidate के experience, skills और interview performance पर depend करेगी)


Interview Details

  • Interview Process:

    • Resume Shortlisting

    • HR Screening

    • Technical Interview (Clinical Research & GCP-based)

  • Interview Mode: Online / Gurgaon office (company decision)


Required Documents

  • Updated Resume / CV

  • Educational Qualification Certificates

  • Experience Letters (if applicable)

  • Government ID Proof

  • Passport (preferred for CRA profile)


How to Apply – Apply Method (Official)

Interested और eligible candidates email के माध्यम से apply कर सकते हैं:

📩 Email IDs:

📌 Email Subject Line:
MED-CRA-001-2026


Location

📍 Gurugram, Haryana (Delhi NCR)


FAQs (Content)

Q1. Is this job suitable for freshers?
This role prefers candidates with clinical research experience, but strong profiles may be considered.

Q2. Is travel mandatory for CRA jobs?
Yes, the CRA role includes site visits, so travel is required.

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

Q4. Does medONE Solution charge any application fee?
No, there is no application or registration fee.


Final Conclusion

यदि आप Clinical Research Associate (CRA) के रूप में pharma industry में stable और growth-oriented career चाहते हैं, तो medONE Solution की यह vacancy एक excellent opportunity है। Reputed CRO के साथ काम करने से candidates को global clinical research exposure मिलता है और future career growth के strong chances बनते हैं।

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


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