Clinical Study Manager

ICON plc • Blue Bell, SD

1d

About The Position

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Clinical Study Manager at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Proven experience in clinical study management, with a strong understanding of the drug development process and regulatory requirements.
• Excellent project management skills, including the ability to handle multiple tasks simultaneously and prioritize effectively.
• Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external partners.
• Detail-oriented with a focus on ensuring data accuracy and maintaining high-quality standards in clinical trials.

Nice To Haves

• Solid clinical trial management experience, with the ability to manage competing priorities and develop your team.

Responsibilities

• Oversee the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and project timelines.
• Collaborate with cross-functional teams, including investigators, vendors, and internal stakeholders, to drive the successful implementation of clinical studies.
• Develop and manage study budgets, resources, and timelines, ensuring efficient use of resources and adherence to study plans.
• Lead the resolution of issues and challenges that may arise during clinical trials, employing effective problem-solving skills and communication strategies.
• Ensure data integrity and quality by implementing rigorous monitoring and validation processes throughout the study lifecycle.

Benefits

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level