Clinical Research Coordinator Job at Green Key Resources, Reading, PA

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  • Green Key Resources
  • Reading, PA

Job Description

The ideal candidate will have patient-facing experience and at least 1 year of experience as a study coordinator in a clinical trial setting. Phlebotomy training/experience, laboratory sample processing experience, and ECG training are strongly preferred.

Responsibilities:

  • Coordinate and oversee clinical research studies in accordance with protocols and regulatory requirements.
  • Recruit, screen, and enroll eligible participants for studies.
  • Obtain informed consent from participants and maintain documentation.
  • Perform or assist with clinical procedures, such as phlebotomy, ECGs, and laboratory sample processing.
  • Collect, record, and maintain study data and source documents.
  • Communicate effectively with study sponsors, investigators, and study team members.
  • Ensure compliance with study protocols, regulations, and institutional policies.
  • Participate in study meetings, trainings, and audits as required.

Qualifications:

  • Bachelor's degree in a health-related field or equivalent experience.
  • Minimum of 1 year of experience as a study coordinator in a clinical trial setting.
  • Patient-facing experience/background is essential.
  • Phlebotomy training/experience is strongly preferred.
  • Laboratory sample processing experience is strongly preferred.
  • Trained to perform ECGs is strongly preferred.
  • Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
  • Excellent communication, organization, and interpersonal skills.
  • Ability to work independently and as part of a team.
  • Detail-oriented with strong problem-solving skills.

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