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ICON Hiring Site Specialist II (Clinical Research) – Bangalore & Chennai | 3+ Years
ICON plc
Bangalore
Chennai
3+ Years
Clinical Research
📄 Job Overview
ICON plc is hiring Site Specialist II for its Site Activation team in India. This role focuses on clinical trial site start-up, regulatory coordination, and contract support for global clinical studies.
🧭 Key Responsibilities
- Support study start-up and essential document review.
- Manage green light and site activation timelines.
- Customize Informed Consent Forms (ICFs).
- Coordinate ICF translations and submissions.
- Handle EC / IRB submissions and regulatory documents.
- Maintain accurate records in eTMF systems.
- Support clinical trial contracts and amendments.
- Collaborate with global cross-functional teams.
🎓 Eligibility Criteria
- B.Pharm, M.Pharm, Pharm.D
- MSc / BSc Life Sciences
- Relevant Bachelor’s degree
- Minimum 3+ years site start-up experience
🧠 Required Skills
- ICF customization & translation workflows
- IRB / EC submission processes
- Clinical trial contract workflows
- Strong documentation & organizational skills
- Excellent communication skills
💼 Why Join ICON?
- Global CRO with strong brand value
- People-first & inclusive work culture
- Competitive salary & global benefits
- Career growth in international trials
📌 Note Before You Apply:
Kindly read the entire job description carefully before applying.
Kindly read the entire job description carefully before applying.
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