Biosampling Project Manager at ICON plc · São Paulo

Biosampling Project Manager
Location: Mexico, Mexico City
Home Based - México
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

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.

What You Will Do:
Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability.

Key responsibilities include:
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.

Your Profile:
You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:
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.

Additional Locations: Brazil, Sao Paulo