Senior Clinical Trial Manager

Senior Clinical Trial Manager - Detalhes da Vaga. ● 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. ●#J-18808-Ljbffr. Requisitos para participar do processo. ● . O que oferecemos.