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Senior Global Clinical Trial Manager (Waltham, MA)
Senior Global Clinical Trial Manager (Waltham, MA)ICON Strategic Solutions • Waltham, MA, US
Senior Global Clinical Trial Manager (Waltham, MA)

Senior Global Clinical Trial Manager (Waltham, MA)

ICON Strategic Solutions • Waltham, MA, US
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ICON has opened a Senior Global Clinical Trial Manager position, and I wanted to see if you are interested.

This position will be, direct hire with full benefits, 3 days in the office (900 Winter St, Waltham, MA 02451) with 2 days remote from home, with pay up to $155k (No bonus)

Please let me know if you are interested in finding out more about this opportunity?

Senior Global Clinical Trial Manager

What you will be doing :

  • Clinical Trial Management with, deliverable, budget, vendor management, along with vendor and site oversite and training.
  • Budget Oversight Oversee the clinical portion of the budget to ensure efficient resource allocation.
  • Ensuring Effective Study Oversight : Develop monitoring plans and tools, ensuring effective study oversight.
  • Optimizing Performance : Train and mentor Clinical Research Associates (CRAs) to optimize their performance.
  • Timely Study Start-Up & Enrollment : Drive enrollment and lead study start-up activities, adhering to timelines.
  • Improving Study Integrity Review trip reports and implement corrective and preventative action plans when necessary.
  • Building Productive Relationships : Foster productive relationships with Sponsors, vendors, and cross-functional teams.

Your profile :

  • Currently, or recently, working at a CRO, Pharmaceutical or Biotechnology company.
  • A minimum of 4+ years of experience in a Global Clinical Trial Management position at a CRO or Pharmaceutical Organization.
  • Clinical Trial Management experience including trial deliverable, trial budget, vendor management, along with vendor and site oversite and training.
  • Experience as a Clinical Trial Manager running Phase 1 trials
  • Bachelor's degree in health, life sciences, or other relevant fields of study.
  • At least 10+ years of relevant clinical experience
  • Preferred : 2+ years of monitoring experience.
  • Experience in managing complex or global trials is advantageous.
  • Experience in managing trial components from start-up to database lock.
  • Experience in coaching / mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.
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