ICON plc is a global leader in healthcare intelligence and clinical research, dedicated to advancing medical research from molecule to medicine. With a focus on innovation and excellence, ICON provides outsourced services to pharmaceutical, biotechnology, medical device companies, and public health organizations.
At ICON, we prioritize patient-centric clinical research, accelerating the development of life-saving drugs and medical devices. Our inclusive work culture fosters professional growth, collaboration, and high performance, making ICON a preferred employer in the clinical research industry.
Current Job Openings at ICON plc
1. Pharmacovigilance Reporting Associate
Locations: Chennai, Trivandrum
Requisition ID: JR126918
Job Description:
- Submit expedited Serious Adverse Event (SAE) reports, Periodic reports, and line listings to regulatory authorities, clients, and investigators.
- Ensure compliance with ICON SOPs, regulatory guidelines (ICH-GCP), and client requirements.
- Maintain safety reporting databases and support audits/inspections.
- Collaborate with cross-functional teams and mentor junior associates.
- Travel (10% domestic/international) may be required.
Qualifications:
- Strong understanding of pharmacovigilance regulations and safety reporting.
- Experience in regulatory submissions and pharmacovigilance operations.
- Excellent organizational and communication skills.
2. Clinical Validation Analyst
Locations: Bangalore, Chennai, Trivandrum
Requisition ID: JR126145
Job Description:
- Perform data validation and quality checks for clinical trial data integrity.
- Conduct SAS listing, edit check testing, and UAT testing.
- Collaborate with teams to develop validation protocols and resolve discrepancies.
- Ensure compliance with EDC Clinical Systems and regulatory standards.
Qualifications:
- Degree in Life Sciences, Statistics, or Computer Science.
- 2-5 years in clinical data management or validation.
- Strong analytical skills and knowledge of EDC systems.
3. Study Start-Up Associate II / Site Activation Specialist II
Locations: Bangalore, Chennai
Requisition ID: JR129756
Job Description:
- Lead regulatory submissions (EC/IRB approvals, CTAs) for clinical trials.
- Coordinate with investigators, sponsors, and regulatory bodies.
- Maintain study start-up documentation and ensure compliance with ICH-GCP.
- Support process improvements for faster trial initiation.
Qualifications:
- Bachelor’s in Life Sciences or related field.
- 2+ years in study start-up, regulatory affairs, or clinical research.
- Strong project management and communication skills.
Why Join ICON plc?
✅ Global Impact: Contribute to life-changing clinical research.
✅ Career Growth: Continuous learning and leadership opportunities.
✅ Work-Life Balance: Flexible benefits, health insurance, and wellness programs.
✅ Inclusive Culture: Equal opportunity employer fostering diversity.
How to Apply?
Application Link For Pharmacovigilance Reporting Associate
Application Link For Clinical Validation Analyst
Application Link For Study start up Associate II/ Site Activation Specialist II
