ICON Plc is a world-leading healthcare intelligence and clinical research organization, dedicated to advancing medical innovation and improving patient outcomes. With a strong commitment to inclusivity, excellence, and cutting-edge research, ICON offers dynamic career opportunities in clinical development, pharmacovigilance, and site management.
Open Positions at ICON Plc
1. Project Associate – Office Based (Bangalore)
Job ID: JR132192 | Location: Bangalore | Job Type: Full-time
Key Responsibilities:
- Organize project team/client meetings, prepare agendas, and document minutes.
- Manage study documentation, trackers, and financial processes (POs, invoices).
- Maintain electronic trial master files (eTMF) and ensure compliance.
- Support project managers with administrative and reporting tasks.
Eligibility:
- Bachelor’s degree in business, finance, health sciences, or related fields.
- Experience in CRO/pharma/clinical research is a plus.
- Proficiency in MS Office (Excel, PowerPoint, Outlook).
- Strong organizational and communication skills.
2. Safety Scientist – Office/Home Based (Bangalore)
Job ID: JR131688 | Location: Bangalore | Job Type: Full-time
Key Responsibilities:
- Conduct safety surveillance, signal detection, and risk management for clinical trials.
- Prepare aggregate safety reports (PSURs, DSURs, RMPs).
- Support pharmacovigilance agreements, PSMF maintenance, and regulatory submissions.
- Collaborate with cross-functional teams on safety data analysis.
Eligibility:
- Bachelor’s/Master’s in life sciences, pharmacy, or related fields.
- Experience in pharmacovigilance/drug safety (pharma/CRO).
- Knowledge of ICH-GCP, FDA/EMA regulations.
- Strong analytical and medical writing skills.
3. Site Specialist II – Office/Home Based (Bangalore/Chennai)
Job ID: JR129390 | Location: Bangalore/Chennai | Job Type: Full-time
Key Responsibilities:
- Manage site activation, contracts, and IRB submissions for clinical trials.
- Customize Informed Consent Forms (ICFs) and coordinate translations.
- Support study start-up, site contracts, and eTMF documentation.
- Liaise with investigators, sponsors, and regulatory bodies.
Eligibility:
- Bachelor’s degree in life sciences, business, or related fields.
- Experience in site start-up, contracts, and IRB processes.
- Strong communication and negotiation skills.
- Ability to work in flexible shifts (global team collaboration).
Why Join ICON Plc?
ICON offers competitive salaries and industry-leading benefits, including:
✅ Health insurance for you & family
✅ Retirement savings plans
✅ Global Employee Assistance Program (TELUS Health)
✅ Flexible leave policies & work-life balance initiatives
✅ Life assurance & wellness programs
How to Apply?
Application Link for Project Associate
