ICON is the world’s largest and most comprehensive clinical research organization, driven by healthcare intelligence and innovation. With a strong commitment to improving patient lives, ICON provides robust clinical trial management, strategic consulting, and data analytics solutions.
Joining ICON means becoming part of a collaborative, growth-driven environment where professionals are empowered to excel. The company fosters a culture of continuous learning, diversity, and inclusion, making it a preferred employer in the clinical research industry.
Job Description: Clinical Research Associate (CRA) – Oncology
As a Clinical Research Associate (CRA), you will play a pivotal role in managing clinical trial sites, ensuring high-quality data collection, compliance with protocols, and patient safety.
Key Responsibilities:
✔ Conduct site selection, initiation, routine monitoring, and close-out visits
✔ Ensure regulatory compliance (ICH-GCP, local regulations)
✔ Oversee data quality, query resolution, and audit readiness
✔ Mentor and support junior team members
✔ Collaborate with investigators, sponsors, and study teams
✔ Maintain strong site relationships for smooth trial execution
Requirements:
✅ Education: B.Pharm / M.Pharm / Pharm D / BDS / MBBS
✅ Experience: Minimum 2 years in onsite monitoring (Oncology trials mandatory)
✅ Skills: Strong communication, problem-solving, and attention to detail
✅ Location: Must be based in Delhi/NCR
Why Join ICON?
🔹 Global Leader in clinical research with career growth opportunities
🔹 Work-life balance with flexible and remote options (#LI-remote)
🔹 Competitive salary, benefits, and professional development programs
🔹 Impactful work contributing to life-saving medical research
