.Clinical Trial Manager II and Senior - Mexico & Brazil - RemoteICON plc is a world-leading healthcare intelligence and clinical research organization.
We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.At ICON, it's our people that set us apart.
Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity.
We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point.
In short, to be the partner of choice in drug development.That's our vision.
We're driven by it.
And we need talented people who share it.If you're as driven as we are, join us.
You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.The Role:We are currently seeking a Clinical Trial Manager II and Sr. CTM in the Biotech Division, aligned with therapeutic areas such as General Medicine (NASH), Rare Diseases, or Oncology, to join our dynamic and diverse team.
As a Clinical Trial Manager at ICON, you will lead global clinical trials, interpret complex medical data, and contribute to the development of groundbreaking treatments and therapies.What You Will Be DoingLeading and managing all aspects of global clinical trial activities, from planning and execution to close-out.Collaborating with cross-functional teams to develop trial protocols, study plans, and strategies.Monitoring trial progress to ensure adherence to timelines, budgets, and quality standards.Managing relationships with third-party vendors, including selection, oversight, and performance evaluation.Providing leadership, guidance, and mentorship to project teams, fostering effective communication and problem-solving.Participating in sponsor meetings, investigator meetings, and bid defense meetings as a key contributor.Your ProfileExperience:At least 3.5 years of experience in a Clinical Trial Management position (CTM II level).Minimum 5 years of experience for consideration at the Senior CTM level.Global trial management experience is required, with a strong focus on the US and Canada.Experience working with the Advarra Ethics Committee is highly desirable.At least 3+ years of monitoring experience is strongly preferred.Prior experience managing all trial components (from start-up to database lock) is preferred.Education:Bachelor's degree in a health, life sciences, or other relevant field, required.Skills:Demonstrated ability to manage complex or global clinical trials