Are you an experienced Clinical Trial Manager looking for an exciting opportunity in Bangalore? ICON plc, a global leader in clinical research and healthcare intelligence, is hiring for a Clinical Trial Manager role. If you have a strong background in clinical trial management, monitoring, and regulatory compliance, this could be your next career move!
About ICON plc
ICON plc is a world-leading clinical research organization (CRO) providing outsourced services to pharmaceutical, biotechnology, medical device, and public health organizations. With a mission to accelerate drug and device development, ICON ensures patient safety, data integrity, and compliance with global regulations.
Job Details
- Position: Clinical Trial Manager
- Location: Bangalore, India (Office-based)
- Job ID: 2024-115190
- Department: ICON Strategic Solutions – Clinical Trial Management
Key Responsibilities
As a Clinical Trial Manager, you will:
- Lead Local Study Teams, ensuring compliance with ICH-GCP, company SOPs, and local regulations.
- Oversee monitoring activities, review reports, and conduct co-monitoring/QC visits.
- Develop Local Monitoring Plans and ensure timely delivery of high-quality data.
- Manage investigator selection, site feasibility, and patient recruitment strategies.
- Coordinate regulatory submissions (EC/IRB, Regulatory Authority) with the Regulatory Affairs team.
- Ensure proper documentation, study master file maintenance, and audit readiness.
- Facilitate investigator meetings, study budgets, and drug supply management.
- Collaborate with global study teams to meet project milestones.
Qualifications & Experience
Essential Requirements:
- Bachelor’s degree in Life Sciences or related field.
- Minimum 5 years of on-site clinical monitoring experience (CRA/Senior CRA).
- At least 2 years of Clinical Trial Management experience in a global CRO or Pharma company.
- Strong knowledge of ICH-GCP, local regulations, and clinical trial processes.
- Excellent communication, leadership, and problem-solving skills.
- Must be based in Bangalore and willing to work in an office-based setup.
Desired Skills:
- Proficiency in English (written and spoken).
- Experience with eTMF, EDC, and clinical trial management systems (CTMS).
- Ability to work in a fast-paced, global clinical research environment.
How to Apply?
If you meet the qualifications and are ready to take on this challenging yet rewarding role, apply now!
📌 Job Reference ID: 2024-115190
📍 Location: Bangalore, India
