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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