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Drug Safety Associate (Pharmacovigilance) Job at Syneos Health

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Syneos Health hiring Drug Safety Associate in Hyderabad and Gurugram for pharmacovigilance professionals with ICSR experience and hybrid work opportunity

Introduction

A promising opportunity is available for professionals in pharmacovigilance with Syneos Health. The organization is currently hiring Drug Safety Associates to support drug safety and case processing activities. This role is ideal for candidates with experience in Individual Case Safety Reports (ICSR) who want to advance their career in clinical research and drug safety operations.

With a hybrid work model and exposure to global safety processes, this position offers a strong platform for professional growth in pharmacovigilance.


Company Overview

Syneos Health is a leading contract research organization (CRO) providing integrated clinical development and commercialization services to pharmaceutical and biotechnology companies. The company supports clinical trials, regulatory processes, and safety monitoring across global markets. Known for its collaborative approach and advanced research capabilities, Syneos Health offers a dynamic environment for professionals in clinical research and pharmacovigilance.


Job Overview

Job TitleDrug Safety Associate / Safety & PV Specialist I
Company NameSyneos Health
LocationHyderabad & Gurugram
Employment TypeFull-Time, Permanent
QualificationAny Graduate / Any Postgraduate
Experience2.5 – 4.5 Years
Salaryβ‚Ή5.5 – β‚Ή6.5 LPA
Application ModeOnline Application

Job Location & Employment Type

This role is available in Hyderabad and Gurugram with a hybrid work model, allowing a combination of on-site and remote working. It is a full-time, permanent position within the pharmacovigilance and drug safety department.


Open Positions / Department Details

  • Role: Safety & Pharmacovigilance Specialist I
  • Department: Research & Development (Drug Safety / Pharmacovigilance)
  • Industry: Clinical Research / Contract Research Organization (CRO)
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Key Roles & Responsibilities

  • Perform ICSR (Individual Case Safety Report) processing including case intake, booking, and triage
  • Handle various case types such as spontaneous reports, clinical trial cases, and literature-based cases
  • Ensure accurate data entry and coding of adverse events using standard medical dictionaries
  • Maintain compliance with global pharmacovigilance guidelines and regulatory requirements
  • Conduct quality checks and ensure timely case processing
  • Communicate effectively with internal teams and stakeholders
  • Maintain proper documentation and reporting standards

Eligibility Criteria

Education:

  • Any Graduate or Postgraduate in relevant fields (Life Sciences preferred)

Experience:

  • 2.5 to 4.5 years of experience in pharmacovigilance or drug safety
  • Hands-on experience in ICSR case processing is mandatory

Skills Required:

Technical Skills:

  • Expertise in ICSR case processing (booking and triage)
  • Knowledge of spontaneous, clinical trial, and literature case handling
  • Understanding of pharmacovigilance workflows and regulations
  • Familiarity with medical terminology and safety databases

Soft Skills:

  • Strong written and verbal communication skills
  • Attention to detail and accuracy
  • Ability to work in a team-oriented environment
  • Time management and multitasking abilities

Salary & Benefits

  • Salary Range: β‚Ή5.5 LPA to β‚Ή6.5 LPA
  • Hybrid working model for better work-life balance
  • Exposure to global pharmacovigilance processes
  • Opportunity to work with a leading CRO organization
  • Career growth in drug safety and clinical research

Selection Process

The hiring process typically includes:

  1. Application screening
  2. Technical interview focused on pharmacovigilance and ICSR knowledge
  3. Practical or case-based discussion
  4. HR interview and final selection

Candidates with strong domain knowledge and relevant experience will have an advantage during the selection process.


How to Apply

Interested candidates should apply through the official job portal of Syneos Health. Ensure your resume highlights your pharmacovigilance experience, ICSR handling expertise, and relevant technical skills.

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Why Apply for This Pharma Job?

This opportunity provides a solid platform for professionals looking to grow in pharmacovigilance and drug safety. Working with a globally recognized CRO like Syneos Health allows candidates to gain exposure to international safety standards, complex case processing, and regulatory requirements.

The hybrid work model, competitive salary, and career advancement opportunities make this role highly attractive for experienced pharmacovigilance professionals aiming for long-term growth in the clinical research industry.


Important Note / Disclaimer

PharmaJobHub.in is an independent job information platform. We do not provide any recruitment guarantee and are not affiliated with any company. Candidates are advised to verify details from official sources before applying.


Final Call-to-Action

If you have relevant experience in pharmacovigilance and are looking for your next career move, apply as soon as possible. Early applications may increase your chances of selection for this role.


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