Clinical Trials Project Manager - Hybrid/Remote

Mass General Brigham

Somerville (MA)

Hybrid

USD 63,000 - 103,000

Full time

7 days ago
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Job summary

Mass General Brigham seeks a detail-oriented Clinical Trials Assistant/Project Manager to oversee multiple trial sites, ensure regulatory documents are complete, and guide site teams in protocol conduct. The role emphasizes accuracy, timely data handling, and collaboration with QA and department managers.

Hybrid work arrangement with on-site requirements at 399 Revolution Drive and remote options. Minimum 2–3 years in clinical trials and data management.

Qualifications

  • Bachelor's Degree is required; degree can be substituted with equivalent experience.
  • 2-3 years of clinical trial experience and data management preferred.

Responsibilities

  • Manage multiple clinical trial sites for the duration of the trial.
  • Collect and review essential regulatory documents before submission to Regulatory for review.
  • Advise research sites on protocol conduct and interpretation and resolve issues.
  • Evaluate data entry quality and manage queries with corrective action plans.
  • Maintain a clinical trial database with latest protocol versions and contact information.
  • Collaborate with department/trial manager to address quality monitoring findings and audits.
  • Prepare official trial correspondence and generate reports from internal/external databases.
  • Assist in training junior staff on key processes and procedures.
  • Support budget development and maintenance for Research Study Maintenance.

Skills

Clinical trial coordination
Regulatory compliance

Education

Bachelor's Degree or equivalent experience

Job description

Mass General Brigham seeks a detail-oriented Clinical Trials Assistant/Project Manager to oversee multiple trial sites, ensure regulatory documents are complete, and guide site teams in protocol conduct. The role emphasizes accuracy, timely data handling, and collaboration with QA and department managers.

Hybrid work arrangement with on-site requirements at 399 Revolution Drive and remote options. Minimum 2–3 years in clinical trials and data management.

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