Clinical Trial Manager Ii

Clinical Trial Manager II - Mexico - 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 RoleWe are currently seeking a Clinical Trial Manager II in the Biotech Division with a therapeutic alignment of Gen Med Nash or Rare Disease or Oncology to join our diverse and dynamic team. As a Clinical Trial Manager II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.What you will be doingLeading and overseeing all aspects of clinical trial management, including planning, execution, and close-out activities.Collaborating with cross-functional teams to develop trial protocols and study plans.Monitoring study progress, ensuring adherence to timelines, budget, and quality standards.Managing vendor relationships and overseeing the selection and oversight of third-party vendors.Providing leadership and guidance to project teams, ensuring effective communication and problem-solving.Participating in Sponsor, investigator, and Bid Defense Meetings.Your ProfileCTM Level II:
1.6 years in a Clinical Trial Management position at a CRO, RequiredBachelor's Degree in a health, life sciences or other relevant field of study, required2+ years of monitoring experience, strongly preferredExperience in managing complex or global trials, preferredMinimum 1 year of experience leading Oncology cellular therapy trials, strongly preferred.Experience in managing all trial components (start-up to database lock), preferredExperience in coaching/mentoring other CTMs, leading a team of CTMs, participating in departmental initiatives, preferredEnglish fluency (ability to read, write, speak), required*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

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