ICON Plc Hiring Clinical Trial Manager

ICON Plc Hiring Clinical Trial Manager – Apply Now in Bangalore

About ICON Plc

ICON Plc is a global leader in healthcare intelligence and clinical research. From molecule to medicine, ICON Plc accelerates drug and device development through outsourced services for pharmaceutical, biotechnology, medical device, and public health organizations. With a strong focus on quality and compliance, ICON Plc ensures that patients benefit from groundbreaking medical advancements.

Job Overview – Clinical Trial Manager

ICON Plc is currently hiring experienced Clinical Trial Managers in Bangalore, India. This role is ideal for professionals passionate about leading clinical studies while ensuring compliance with ICH-GCP guidelines and regulatory requirements.

Key Responsibilities

• Oversee clinical trial commitments, ensuring timely delivery and data quality.
• Lead Local Study Teams, consisting of monitors and study administrators.
• Ensure compliance with ICH-GCP, company policies, and local regulations.
• Develop Local Monitoring Plans and review monitoring visit reports.
• Identify and resolve complex study issues proactively.
• Coordinate with Investigators and ensure smooth recruitment strategies.
• Forecast study timelines, resources, budgets, and material requirements.
• Collaborate with Regulatory Affairs to ensure timely document submissions.
• Manage serious adverse event (SAE) reconciliations and study master file documentation.
• Provide guidance and training to new team members.
• Ensure accurate study-related payments and compliance with audit requirements.

Required Qualifications

Education:

• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or a related field.

Experience:

• 2+ years of Clinical Trial Management experience in a global CRO/Pharma.
• 5+ years of onsite clinical monitoring experience.
• Must be willing to work in an office-based setup in Bangalore.

Essential Skills:

• Strong knowledge of ICH-GCP guidelines and local clinical trial regulations.
• Experience in clinical study processes, data management, and drug handling.
• Excellent communication skills in English (spoken and written).
• Ability to adapt and work efficiently with IT systems.
• Strong leadership and team management abilities.

How to Apply?

If you meet the qualifications and are ready to take the next step in your career, apply now! 👉 Apply Here

Job Summary Table

📢 Don’t miss this incredible opportunity—Apply today and advance your career in clinical research!

Tagged as: Good Clinical Practice (GCP)