Sr Clinical Trial Manager - Hybrid Boston

ICON Strategic Solutions; Boston (MA); On-site; USD 100,000 - 130,000; Full time

Job summary

A clinical solutions company in Boston is seeking a Senior Clinical Trial Manager to enhance trial execution and oversight. In this pivotal role, you will manage clinical budgets, drive enrollment, and mentor CRAs. The ideal candidate will possess over 10 years of experience in clinical trial management, and a bachelor's degree in health or life sciences, with strong leadership and risk management skills. This role promises a dynamic work environment contributing to the success of clinical studies.

Qualifications

• Minimum 4+ years in Clinical Trial Management at a CRO or Pharmaceutical Organization.
• 10+ years of relevant clinical trial management experience.
• Preferred: Phase 1 experience and 2+ years of monitoring experience.

Responsibilities

• Oversee the clinical portion of the budget for resource allocation.
• Develop monitoring plans and ensure effective study oversight.
• Train and mentor Clinical Research Associates (CRAs).
• Drive enrollment and lead study start-up activities.
• Review trip reports and implement corrective action plans.

Skills

Clinical Trial Management

Stakeholder Liaison

Risk Management

Performance Optimization

Problem Solving

Education

Bachelor's degree in health, life sciences, or relevant fields

Job description

Overview

We are currently seeking a Senior Clinical Trial Manager to join our diverse and dynamic team. As the Senior Clinical Trial Manager, you will hold a crucial role in ensuring the successful delivery of all clinical aspects of the studies. Your expertise and leadership will be instrumental in managing the clinical portion of the budget, developing effective monitoring plans, and driving enrollment to meet project objectives. Moreover, you will liaise with stakeholders, identify and mitigate risks, and provide comprehensive reporting on all clinical activities.

What you will be doing

• 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

• A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization.
• Bachelor's degree in health, life sciences, or other relevant fields of study.
• Phase 1 experience preferred
• At least 10+ years of relevant experience in clinical trial management.
• Preferred: 2+ years of monitoring experience.
• Experience in managing complex or global trials is advantageous.
• Preferred: Experience in managing all trial components from start-up to database lock.
• Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.
• Fluency in English (reading, writing, speaking).