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Clinical Research Associate
Clinical Research AssociateVivid Resourcing • Boston, MA, US
Clinical Research Associate

Clinical Research Associate

Vivid Resourcing • Boston, MA, US
[job_card.30_days_ago]
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  • [job_card.full_time]
[job_card.job_description]

Job Description

Job Title: Clinical Research Associate (CRA) – Oncology

Location: Boston, MA (Hybrid or Remote, with travel)


Reports to: Director of Clinical Operations


Our client is a Boston-based biotechnology company dedicated to developing innovative oncology therapies that address unmet medical needs. The team is driven by scientific rigor, patient-centricity, and collaboration to advance cutting-edge cancer treatments from early development through late-stage clinical trials.


Position Summary

The Clinical Research Associate (CRA) will support the planning, execution, and monitoring of oncology clinical trials in compliance with ICH-GCP, FDA regulations, and company SOPs. The CRA will serve as a key liaison between investigative sites and the clinical operations team, ensuring data integrity, patient safety, and operational excellence across assigned studies.


Key Responsibilities

  • Conduct site qualification, initiation, monitoring, and close-out visits for oncology clinical trials
  • Ensure protocol compliance, data accuracy, informed consent integrity, and patient safety
  • Monitor AE/SAE reporting, protocol deviations, and essential documentation
  • Train and support site staff and maintain strong site relationships
  • Review and maintain study documentation and Trial Master File (TMF)
  • Track site performance, identify risks, and proactively resolve issues
  • Collaborate cross-functionally and provide timely monitoring reports
  • Support audit and inspection readiness


Qualifications

  • Bachelor’s degree/Master's degree in Life Sciences, Nursing, or a related field (required)
  • 2+ years of CRA experience in clinical research (oncology preferred)
  • Experience monitoring interventional clinical trials (Phase I–III preferred)
  • Knowledge of Good Clinical Practices (GCP), clinical monitoring, study site oversight and management.
  • Strong knowledge of ICH-GCP and FDA regulations
  • Excellent communication, organizational, and problem-solving skills
  • Ability to manage multiple sites and travel up to 30%


Offer

  • Salary 100-150k (depending on level of experience)
  • Career development opportunities in a growing oncology-focused organization
  • Collaborative, mission-driven work environment in the Boston biotech hub

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