As a Senior Clinical Trial Manager, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
You will play a pivotal role in overseeing the planning, execution, and completion of clinical trials across various therapeutic areas. You will contribute to advancing innovative treatments and therapies through the successful management of trial protocols, timelines, budgets, and cross-functional team collaboration.
What You Will Be Doing:
- Leading the end-to-end management of clinical trials, from study start-up to close-out, ensuring they are conducted in compliance with regulatory requirements and ICON standards.
- Collaborating with cross-functional teams to coordinate trial activities, including study design, protocol development, and investigator site management.
- Monitoring study progress, timelines, and budgets to ensure project milestones are met on time and within scope.
- Managing relationships with investigators, sponsors, and external vendors to ensure smooth trial execution and resolution of any issues.
- Ensuring accurate and timely documentation, data collection, and reporting in line with Good Clinical Practice (GCP) guidelines.
Your Profile:
- Bachelor’s degree in life sciences, nursing, or a related field (Master’s degree preferred).
- Extensive experience in clinical trial management (at least 5 years), with a strong understanding of ICH-GCP guidelines and regulatory requirements.
- Proven ability to lead and manage clinical trial teams in a matrix environment.
- Strong project management skills, with experience in managing timelines, budgets, and resources effectively.
- Excellent communication and interpersonal skills, with the ability to collaborate with diverse teams and stakeholders.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
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