📍 Location: Work from Home / Remote (Bangalore, Trivandrum, Chennai – India)
🎓 Eligibility: B.Pharm, M.Pharm, Pharm.D, MSc, BSc (Life Sciences)
🕒 Experience: Minimum 2 years in informed consent writing/development
Are you a clinical research professional looking for a remote opportunity with a leading global CRO? ICON plc is hiring for the role of Informed Consent Specialist II, and this could be your next big career move!
🔍 About ICON plc
ICON plc is a global provider of outsourced development and commercialisation services to the pharmaceutical, biotechnology, and medical device industries. ICON is known for its innovation, quality, and impact on advancing clinical research.
💼 Job Role: Informed Consent Specialist II
🔑 Key Responsibilities:
- Develop and review Subject Information Sheets (SIS) and Informed Consent Forms (ICFs) for global and country-specific clinical trials.
- Ensure compliance with ICH-GCP guidelines, ICON SOPs, and regional regulatory standards.
- Collaborate with cross-functional teams including Sponsors, SSU PMs, and CTMs.
- Resolve EC/IRB/CA queries and maintain accurate documentation in the Trial Master File (TMF).
- Act as a Subject Matter Expert (SME) and mentor new team members.
- Represent ICON during audits and regulatory inspections.
✅ Required Skills & Qualifications:
- Minimum 2 years of experience in informed consent development.
- Strong written and verbal English communication skills.
- Familiarity with GCP/ICH guidelines and regional regulatory nuances.
- Ability to interpret clinical trial protocols and manage timelines.
- Analytical mindset and attention to detail.
🌟 What’s in it for You?
ICON offers a supportive and flexible work environment with competitive perks:
- 🏖️ Flexible annual leave
- 🏥 Health insurance for you & your family
- 💰 Retirement planning support
- 🧠 Employee Assistance Programme (TELUS Health)
- 🛡️ Life assurance
- 🌍 Country-specific benefits (childcare, gym discounts, travel perks)
📢 Why You Should Apply
This is a verified job listing from a trusted employer in the global pharma industry. If you're passionate about clinical research and want to grow your career in a flexible, remote setting—this role is perfect for you.
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📝 How to Apply?
👉 Apply Now – Informed Consent Specialist II at ICON plc
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