Senior Clinical Trial Lead — Hybrid/Remote

Corbus Pharmaceuticals, Inc.

Norwood (MA)

Hybrid

USD 120,000 - 190,000

Full time

14 days+

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Job summary

Corbus Pharmaceuticals Holdings, Inc. in Norwood, MA seeks a Clinical Trial Manager to lead day-to-day trial execution across phases, coordinating CROs and internal teams.

The role emphasizes risk management, budgeting, and cross-functional collaboration to ensure quality and on-time delivery. Applicants should have advanced knowledge of GCP/ICH guidelines and experience in phase 1–4 trials, preferably oncology.

Qualifications

  • Bachelor’s Degree in health, biologic science or related field.
  • 8+ years clinical study management experience, including 5+ years as lead/PM.
  • Experience managing contracted resources/CROs.
  • Experience in phase 1–4 trials; oncology preferred.
  • Site monitoring and clinical data review experience preferred.
  • Advanced knowledge of GCP and current US/EU/UK regulations.
  • Excellent communication, organizational and leadership skills.

Responsibilities

  • Oversee day-to-day trial execution from initiation through closeout.
  • Coordinate CROs and external vendors to meet milestones and budget.
  • Ensure protocol and regulatory compliance across sites and studies.
  • Lead study team meetings and maintain trackers, action items and logs.
  • Support site and vendor documents, budgets and contracts as needed.
  • Maintain and review Trial Master File and QA activities.

Skills

Study management
Project leadership
GCP/ICH knowledge
Regulatory compliance
Vendor management
Cross-functional collaboration

Education

Bachelor’s Degree in health/science

Job description

Corbus Pharmaceuticals Holdings, Inc. in Norwood, MA seeks a Clinical Trial Manager to lead day-to-day trial execution across phases, coordinating CROs and internal teams.

The role emphasizes risk management, budgeting, and cross-functional collaboration to ensure quality and on-time delivery. Applicants should have advanced knowledge of GCP/ICH guidelines and experience in phase 1–4 trials, preferably oncology.

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