Clinical Research Coordinator

3 weeks ago


Kansas City, United States Kelly Science, Engineering, Technology & Telecom Full time

Kelly Science & Clinical is seeking individuals with clinical trial research experience with an interest in learning and growing in the field of clinical research for an open Clinical Research Coordinator opportunity. The CRC position is Full-time Contract with Potential to convert to Permanent.

Onsite in the southern Kansas City, MO area

No relocation benefits, local candidates only

No C2C

Position Summary: The Clinical Research Coordinator is responsible to support observational clinical studies within various therapeutic areas, with initial focus on Colorectal and Lung Cancer Screening Studies. Our client helps biotechnology companies accelerate the creation of life-saving health screening solutions. This is a full-time opportunity that may require flexibility in working hours to connect with possible patient participants during the study enrollment phase. The opportunity is a long-term contract with possibility to convert to direct hire depending on study needs.

Scope of Work:

The Clinical Research Coordinator will play a critical role in ensuring the success of clinical trials by recruiting study participants, managing study procedures, ensuring regulatory compliance, and confirming that data is collected accurately and completely.

This role would include, but is not limited to, the following:

  • Participant recruitment: Responsible for identifying potential study participants and recruiting them to participate. This involves screening potential participants for eligibility, providing information about the study, and moving willing participants into the Informed Consent phase of the process.
  • Study procedures: Responsible for coordinating and managing the various procedures involved in the study, such as scheduling appointments, helping participants with the informed consent process, and collecting data from participants.
  • Data collection and management: Ensure that data is collected accurately and completely. This involves administering questionnaires and ensuring that data is entered into the study database in a timely and accurate manner.
  • Adverse event monitoring and reporting: Responsible for monitoring study participants for adverse events and ensuring that any adverse events are reported to the appropriate parties in a timely manner.
  • Regulatory compliance: Responsible for ensuring that the study is conducted in compliance with all relevant regulations and guidelines, such as those set forth by the Food and Drug Administration and the International Conference on Harmonization ICH .
  • Communication and collaboration: Works closely with other members of the study team, including the Principal Investigator and Lead Clinical Research Coordinator, to ensure that the study is conducted smoothly and efficiently.

Qualifications:

  • Bachelor s Degree preferred
  • Two years of clinical research experience preferred
  • Experience with patient recruitment, including the Informed Consent Process Electronic Data Capture system experience preferred
  • Good Clinical Practice and ICH experience


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