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Senior Drug Safety Associate Job at ICON plc | Pharmacovigilance Careers 2026

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Looking for pharma jobs and global pharmacovigilance careers? Explore this exciting opportunity with ICON plc in Sofia, Bulgaria offering hybrid work flexibility.

About the Company

ICON plc is a globally recognized clinical research organization known for delivering innovative healthcare intelligence solutions. With a strong commitment to regulatory compliance, patient safety, and scientific excellence, ICON supports pharmaceutical and biotechnology companies worldwide. The organization fosters a culture of innovation, inclusivity, and continuous growth, making it a preferred employer in global pharmaceutical careers.

Job Details

  • Company Name: ICON plc
  • Experience: Senior-level (experience required in pharmacovigilance)
  • Qualification: Life Sciences / Pharmacy or related field
  • Location: Sofia, Bulgaria
  • Work Type: Hybrid (Office with Flex)

Job Description

ICON plc is hiring for a senior-level pharmacovigilance role focused on drug safety operations, regulatory compliance, and patient safety monitoring within global clinical development programs.

Senior Drug Safety Associate

  • Department: Pharmacovigilance / Drug Safety
  • Market: Global Clinical Research
  • Role: Safety data management and regulatory reporting
  • Experience: Senior-level pharmacovigilance experience required
  • Education/Qualification: Life Sciences, Pharmacy, or related discipline

Skills/Qualifications

  • Strong knowledge of pharmacovigilance regulations (ICH, GVP)
  • Experience with adverse event reporting and safety databases
  • Data analysis and signal detection expertise
  • Excellent communication and teamwork skills
  • Regulatory documentation and compliance experience
  • Ability to mentor junior team members

Key Responsibilities

  • Manage adverse event collection and processing
  • Ensure compliance with regulatory reporting timelines
  • Analyze safety data and identify trends
  • Prepare PSURs and regulatory submissions
  • Collaborate with clinical and medical teams
  • Maintain pharmacovigilance databases accuracy
  • Support audits and regulatory inspections
  • Train and guide junior team members

Benefits/Perks

  • Competitive salary and global exposure
  • Hybrid work flexibility
  • Career growth opportunities
  • Learning and development programs
  • Inclusive and innovative work culture
  • Opportunity to work on global clinical trials

How to Apply

Verified Post

Verification: To confirm the legitimacy of this posting, you can view the original announcement on the ICON plc career page.

ICON plc is a globally recognized clinical research organization known for delivering innovative healthcare intelligence solutions.

🔗 Click below to apply directly for this job

Interested candidates can apply directly through the official ICON careers page. Visit the company website or explore trusted pharma job platforms like Pharma Recruiter: https://pharmarecruiter.in

Apply early to secure your opportunity in global pharmacovigilance careers.

Why You Should Join

Joining ICON plc offers long-term career stability in a globally respected CRO. Employees benefit from continuous learning, exposure to international projects, and a strong compliance-driven environment that prioritizes innovation and patient safety.

FAQs

Who can apply for this role?

Candidates with a background in Life Sciences, Pharmacy, or related fields and relevant pharmacovigilance experience can apply.

Is this a remote job?

This role is hybrid, combining office work with flexible arrangements.

How can I apply?

You can apply via the official ICON careers portal or visit Pharma Recruiter for updates.

What career growth opportunities are available?

ICON offers structured career development, training programs, and global exposure in clinical research.

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