"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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"Join ICON as a Due Diligence Specialist in Bangalore & Chennai – Clinical Research Career Opportunity"

"Career Opportunity: Due Diligence Specialist I/II at ICON plc – Bangalore & Chennai"


Are you passionate about clinical research, regulatory compliance, and making a global impact in healthcare? ICON plc, a worldwide leader in healthcare intelligence and clinical research, is offering an exciting opportunity for the position of Due Diligence Specialist I/II in its Bangalore and Chennai offices.

This is a full-time, office-based role with flexible working options, designed for professionals who are eager to contribute to cutting-edge clinical trials and shape the future of healthcare innovation.

Key Responsibilities:-

As a Due Diligence Specialist, your role will be vital in driving success across ICON's clinical trial projects. Responsibilities include:

  • Performing due diligence assessments for clinical sites, investigators, and vendors.
  • Reviewing regulatory documentation and study protocols to ensure compliance and identify risks.
  • Supporting development of effective risk mitigation plans.
  • Coordinating with cross-functional teams to ensure timely and accurate project execution.
  • Maintaining audit-ready documentation of all due diligence processes and outcomes.

Eligibility & Required Skills:-

Educational Background:

  • Bachelor’s degree in Life Sciences, Regulatory Affairs, or related field.

Experience:

  • 1 to 4 years of experience in clinical research, regulatory affairs, or relevant pharmaceutical domains.

Skill Set:

  • Strong attention to detail and analytical thinking.
  • Excellent time management and ability to prioritize tasks under tight deadlines.
  • Effective communication and collaboration skills.
  • Familiarity with global clinical trial regulations is a plus.

Benefits of Joining ICON:-

ICON is known for its dynamic, inclusive culture and commitment to employee well-being. Perks include:

  • Attractive Salary: INR 6–10 LPA, depending on experience.
  • Health Coverage: Comprehensive health insurance for you and your family.
  • Retirement Plans: Long-term savings options to secure your future.
  • Wellness Support: 24/7 mental and emotional support via TELUS Health.
  • Employee Perks: Country-specific benefits like travel discounts, gym memberships, and childcare support.
  • Flexible Work-Life Balance: Generous leave and hybrid work setup.

Job Location:-

  • Bangalore or Chennai, India

How to Apply:-

Interested candidates can apply directly via the official portal:
👉 Apply Here

ICON is an equal opportunity employer and encourages candidates from diverse backgrounds to apply. Take this step forward in your pharma career and be a part of global healthcare transformation!

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