ICON Strategic Solutions
Senior Global Clinical Trial Manager for the Waltham, MA office.
ICON Strategic Solutions, Boston, Massachusetts, us, 02298
Senior Global Clinical Trial Manager – Waltham, MA
ICON Strategic Solutions is seeking a Senior Global Clinical Trial Manager for its Waltham, MA office ( $170k salary, no bonus ). This role is a direct hire with full benefits, 3 days in the office (900 Winter St, Waltham, MA 02451) and 2 days remote from home.
Senior Global Clinical Trial Manager (ICON embedded with Alkermes)
What you will be doing:
Clinical Trial Management with deliverables, budget, vendor management, along with vendor and site oversight 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.
Minimum of 4+ years of experience in a Global Clinical Trial Management position at a CRO or Pharmaceutical Organization.
Experience managing 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 coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.
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Senior Global Clinical Trial Manager (ICON embedded with Alkermes)
What you will be doing:
Clinical Trial Management with deliverables, budget, vendor management, along with vendor and site oversight 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.
Minimum of 4+ years of experience in a Global Clinical Trial Management position at a CRO or Pharmaceutical Organization.
Experience managing 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 coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.
#J-18808-Ljbffr