ICON Careers: Apply Now for Clinical Manager Role
ICON Careers: ICON plc, a global leader in healthcare intelligence and clinical research, is seeking an experienced and motivated Clinical Trial Manager (Study Delivery Manager) to join its high-performing clinical operations team. This role is ideal for professionals who thrive in complex, fast-paced research environments and want to make a meaningful impact in global clinical development.
ICON Careers Job Details:
- Position: Clinical Trial Manager
- Job ID: JR139157
- Location: Bengaluru
ICON Careers—About ICON:
ICON plc is one of the world’s largest and most respected Contract Research Organisations (CROs), headquartered in Dublin, Ireland, and operating across 119 locations in 53 countries.
ICON specialises in:
- End-to-end clinical development solutions
- Real-world evidence & healthcare analytics
- Regulatory, safety, and biometrics services
- FSP (Functional Service Provider) partnerships with top global pharma & biotech companies
ICON’s mission is to accelerate the development of life-changing medicines and medical devices. With a strong culture of innovation, diversity, and scientific excellence, ICON is recognised globally as an industry leader driving the future of clinical research.
ICON Careers—Qualifications & Experience
- University degree in medicine or an equivalent combination of education and experience.
- Proven ability to lead and deliver operational aspects of a clinical study.
- Subject-matter expertise in a relevant therapeutic area.
- Prior experience in clinical monitoring is preferred.
- Strong communication, decision-making, and stakeholder management skills.
- Ability to travel up to 20% as required.
Role
The clinical trial manager will lead the planning, execution, and oversight of global clinical trials, ensuring high-quality delivery within established timelines, budgets, and regulatory guidelines. You will serve as a key decision-maker, collaborator, and strategic leader throughout the study lifecycle.
Key Responsibilities
- Plan, coordinate, and manage all operational aspects of clinical trials.
- Ensure study delivery aligns with timelines, budget targets, and quality standards.
- Develop, review, and implement trial protocols, operational plans, and processes.
- Lead cross-functional teams and maintain strong site and investigator relationships.
- Oversee risk management, vendor selection, and issue resolution throughout the trial.
- Ensure compliance with ICH-GCP, regulatory requirements, and ethical standards.
- Provide strategic guidance to internal and external stakeholders.
- Monitor study progress, prepare reports, and support inspection readiness.
- Problem-solve proactively to ensure uninterrupted trial delivery.
