Clinical Trial Manager II

Há 3 dias


São Paulo, Brasil myGwork - LGBTQ+ Business Community Tempo inteiro

Clinical Trial Manager II - Mexico - Remote

ICON 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.

The Role

We 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 doing

  • Leading 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.
  • Participate in Sponsor, investigator, and Bid Defense Meetings.
Your Profile

CTM Level II:

  • 1.6 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
  • 2+ years of monitoring experience, strongly preferred
  • Experience in managing complex or global trials, preferred
  • Minimum 1 year of experience leading Oncology cellular therapy trials, strongly preferred.
  • 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

*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.

  • Competitive salary packages.
  • Annual bonuses reflecting performance goals.
  • Range of health-related benefits to employees and their families.
  • Competitive retirement plans and related benefits.
  • Supportive environment for personal and professional growth.

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.

Interested in the role, but unsure if you meet all of the requirements? We encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON.

Are you a current ICON Employee? Please click here to apply.

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