Clinical Research Coordinator

Found in: Appcast Linkedin GBL C2 - 2 weeks ago

Kansas City, United States Kelly Services Full time

Clinical Research Coordinator


  • Opportunity: Temp to potential permanent employment
  • Location: Onsite in KS, MO
  • Length: No end date and their goal is to convert to direct hire in future
  • Benefits/Pay: Contract benefit options available, W2 Hourly Pay based on experience


Kelly Science and Clinical is currently hiring a Clinical Research Coordinator for one of our clients who supports biotechnology companies accelerate the creation of life-saving health screening solutions. We are seeking a motivated and detail-oriented Clinical Research Coordinators to join their dynamic team and contribute to groundbreaking research studies and trials. The Clinical Research Coordinator will play a critical role in ensuring the success of clinical trials by recruiting study participants (recruiting mostly by phone), collecting ICF's, 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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