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Senior Clinical Trial Manager

ICON Public Limited Corporation

Remote, Multiple US s

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.

What will you be doing

The Clinical Trial Manager in the Biotech Division with a therapeutic alignment of NASH studies is responsible for the delivery of all clinical aspects of the study. The CTM oversees the clinical portion of the budget, develops monitoring plans & tools, trains CRAs, drives enrollment and study start-up activities, reviews trip reports, implements corrective and preventative action plans, liaises with the Sponsor, vendors and cross-functional teams, identifies and mitigates risks that may impact clinical delivery, and provides reporting and metrics on all clinical activities. The CTM will also participate in Sponsor, Investigator and bid defense meetings.

Your Profile

Level 2:

  • 2+ years in a Clinical Trial Management position at a CRO, Required
  • Bachelor’s Degree in a health, life sciences or other relevant field of study, required
  • 8+ years of relevant experience, required
  • 2+ years of monitoring experience, strongly preferred
  • Experience in managing complex or global trials, preferred
  • Current/Prior NASH experience
  • Experience in managing all trial components (start-up to database lock), preferred
  • Experience in coaching/mentoring other CTMs, leading a team of CTMs, participating in departmental initiatives, preferred
  • English fluency (ability to read, write, speak), required
  • Travel of up to a maximum of 10%, required

Level 3:

  • 4-5+ years in a Clinical Trial Management position at a CRO, Required
  • Bachelor’s degree in a health, life sciences or other relevant field of study, required
  • 10+ years of relevant experience, required
  • 2+ years monitoring experience, strongly preferred
  • Experience in managing complex or global trials, preferred
  • Current/Prior NASH experience
  • Experience in managing all trial components (start-up to database lock), preferred
  • Experience in coaching/mentoring other CTMs, leading a team of CTMs, participating in departmental initiatives, preferred
  • English fluency (ability to read, write, speak), required
  • Travel of up to a maximum of 10%

To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa stat

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.

Job posted: 1970-01-01

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