Clinical Research Coordinator

4 weeks ago


Chicago, Illinois, United States Research by Design, LLC Full time
Job Summary

We are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our team at Research by Design, LLC. The successful candidate will be responsible for developing and implementing strategies to recruit participants for clinical research studies, conducting initial screenings, and maintaining accurate records of recruitment activities.

Key Responsibilities

  • Develop and implement participant recruitment strategies to meet enrollment targets and timelines.
  • Conduct initial screenings of potential participants to determine eligibility based on study criteria and protocols.
  • Build and maintain relationships with local healthcare providers, community organizations, and patient advocacy groups to increase awareness of ongoing clinical trials.
  • Maintain accurate and up-to-date records of potential participants, recruitment activities, and screening outcomes using study-specific databases and electronic health records (EHR).
  • Assist in obtaining informed consent from participants, ensuring they understand the study's purpose, risks, and benefits.
  • Collaborate with clinical study coordinators, principal investigators, and research teams to meet enrollment targets and timelines.
  • Provide regular updates on recruitment progress, including metrics such as the number of screened, eligible, and enrolled participants.
  • Ensure that recruitment activities comply with ethical guidelines, Good Clinical Practice (GCP), Institutional Review Board (IRB) requirements, and all applicable regulations.
  • Stay up-to-date with industry developments and best practices in clinical research recruitment.

Requirements

  • Previous experience in clinical research, patient recruitment, or a related healthcare role is preferred.
  • Strong understanding of clinical trial processes and ethical considerations in recruitment.
  • Excellent communication and interpersonal skills, with the ability to interact with diverse populations.
  • Ability to work independently and as part of a team in a fast-paced, dynamic environment.
  • Proficiency in using electronic medical records (EMR) systems, clinical trial management systems (CTMS), and basic office software (Microsoft Office Suite).


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