Job Description

ICON is seeking Senior Global Clinical Trial Manager for the Waltham, MA office. Pay up to $170k (No bonus)

As the Senior Global Clinical Trial Manager, will be responsible for Running global clinical trials, trial deliverable, trial budget, trial vendors, CRA and Site operational oversite and training. Following monitoring plans and reviewing trip reports.

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 $170k (No bonus)

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

Senior Global Clinical Trial Manager (ICON embedded with Alkermes)

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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