Senior Clinical Trial Manager

• 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 Senior Clinical Trial Manager 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 doing:Leading 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.
• To be successful in the role, you will have:Experience:Minimum 4.
• 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.
• Experience in coaching and mentoring other CTMs, leading teams, and contributing to departmental initiatives.
• Strong proficiency in English (spoken and written) is required.
• For candidates based in Brazil, comfort with Spanish is an advantage.
• *Please submit CV/Resume in English.
• *Benefits of Working in ICON:Our success depends on the quality of our people.
• That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.
• We offer very competitive salary packages.
• And to keep them competitive, we regularly benchmark them against our competitors.
• Our annual bonuses reflect delivery of performance goals - both ours and yours.
• We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
• But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
• ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment.
• All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
• If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
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