Clinical Trials Coordinator I-III

2 weeks ago


Philadelphia, Pennsylvania, United States Medix™ Full time

Clinical Research Coordinator - Medix™

Job Overview

The Clinical Research Coordinator plays a pivotal role in overseeing and facilitating the execution of clinical research protocols, which may be funded by various sources including industry, cooperative groups, or grants. This position is essential in ensuring the effective management and operation of clinical research initiatives, focusing on participant recruitment, adherence to protocols, participant safety, and data integrity.

Key Responsibilities

  • Lead the coordination of clinical research protocols, ensuring compliance and participant safety.
  • Collaborate with clinical research team members to develop monitoring tools for trial accrual and timely study activation.
  • Engage with institutional investigators and healthcare team members to support the execution of clinical trials.
  • Maintain flexibility in work schedules to cover study responsibilities effectively.

Qualifications

  • Bachelor's Degree (Required)
  • Master's Degree (Preferred)

Certifications

  • CCRC - Certified Clinical Research Coordinator (Preferred)
  • CCRP - Certified Clinical Research Professional (Preferred)
  • CCRA - Certified Clinical Research Associate (Preferred)

Experience

  • Minimum of 2 years in clinical research (Required)
  • At least 2 years of experience with oncology clinical trials (Required)
  • Knowledge of chemotherapy and/or radiation therapy administration (Required)

General Duties

  • Adhere to all relevant policies, procedures, and regulations, including patient confidentiality laws.
  • Promote and uphold safety standards within the clinical environment.
  • Participate in staff meetings and complete required training and evaluations.
  • Stay informed about developments in clinical research and maintain competency in patient care.

Communication and Collaboration

  • Act as a liaison between investigators and pharmaceutical firms, ensuring effective communication.
  • Foster collaborative relationships with research participants and team members across disciplines.
  • Coordinate evaluations of clinical research studies and provide feedback to relevant parties.

Participant Coordination

  • Assist in identifying potential research participants for ongoing clinical trials.
  • Ensure eligibility requirements are met prior to participant registration.
  • Monitor and report adverse events and treatment toxicities.

Research Administration

  • Design and manage systems for organizing clinical research workflows.
  • Ensure compliance with federal and institutional guidelines to protect participant rights.
  • Conduct evaluations of clinical research activities and recommend improvements.

Quality Assurance

  • Evaluate protocol study forms for accuracy and compliance.
  • Assist in gathering source documents for audits and site visits.
  • Work with quality assurance teams to meet regulatory standards.

This role at Medix™ is crucial for advancing clinical research initiatives and ensuring the highest standards of participant care and data quality.



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