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Clinical Research Coordinator (GI team)

  • Philadelphia, PA, United States

From $30 USD / hour

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Job details

Pay
From $30 USD / hour
Experience
2+ years of clinical research experience, preferably supporting oncology studies, Phase 1 studes, or high-acuity, high-volume industry-sponsored clinical trials.
Posting language
English
Posted

Original job description

Required Skills & Experience

  • 2+ years of clinical research experience, preferably supporting oncology studies, Phase 1 studes, or high-acuity, high-volume industry-sponsored clinical trials.
  • Hands-on experience coordinating interventional drug trials, including patient enrollment, informed consent, visit coordination, ordering protocol-required labs and imaging, and interaction with study monitors.
  • Strong understanding of clinical trial protocols and the ability to execute study procedures in compliance with protocol, GCP, and regulatory requirements.
  • Experience working directly with patients on clinical research drug trials.
  • Excellent organizational skills with the ability to manage multiple studies and priorities in a fast-paced environment.

Nice to Have Skills & Experience

Oncology experience Bachelors or Masters Degree

Job Description

A large healthcare provider in Philadelphia, PA is seeking a Sr Clinical Research Coordinators to support its growing clinical research program. These are newly created positions driven by continued expansion of the research team and clinical trial portfolio.

The Clinical Research Coordinator will play a key role in the day-to-day management of oncology clinical trials, ensuring studies are conducted in compliance with protocol requirements, Good Clinical Practice (GCP) guidelines, and institutional policies. This individual will work closely with investigators, patients, sponsors, and research staff to coordinate study activities from startup through closeout.

Responsibilities include managing clinical trial operations, obtaining informed consent from study participants, coordinating patient visits, supporting orientation and training activities, overseeing central laboratory processes, maintaining study documentation, preparing for monitor visits, assisting with data collection and management, completing study reports, supporting low-risk institutional trial submissions, and tracking IRB submissions, approvals, and renewals.

This is an excellent opportunity to join a nationally recognized cancer center and contribute to cutting-edge oncology research that directly impacts patient care and treatment outcomes.

More about this job

Skills

  • Clinical research
  • Clinical trials
  • Regulatory compliance
  • Google Cloud
  • Organizational skills
  • Research
  • Documentation

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