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Clinical Research Coordinator

Miami, FL

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Description

Start-up clinical research facility in the Blue Lagoon area is looking for a Clinical Research Coordinator.

 

Schedule:

Mon-Fri

9am - 5:30pm or 8:30 - 5:00pm (depending on preference/or demand)

May need to come in early to help patients.

 

Payrate:

40k-50k depending on experience

 

Requirements:

  • Associates degree in a clinical or scientific related discipline desired.

  • 3-5 years of research experience performing clinical research.

  • Prior experience in a medical environment is a plus.

  • The ability to communicate in English and Spanish, the ability to communicate in English is particularly important.

  • The ability to multi-task is a must.

  • Willingness to participate in training and education programs.

  • A reliable means of transportation is required for this position.

  • Knowledge of medical terminology. 

  • The ability to work independently. 

Duties:

  • Dominates the general aspects of the protocol and the Informed Consent Form (ICF).Participates in the informed consent process, detailing the patient and enrolling patients on protocol.

  • Collects and monitors the collection and processing of patient samples, in accordance with the protocol.Checks to ensure accuracy of the data consistent with the study protocol.

  • Performs diagnostic evaluations such as ECGs.

  • Participates in the creation of source documents.

  • Participates in required training and education programs for each trial, and for continued education.

  • Maintains strict patient confidentiality according to HIPPA regulations and applicable law.

  • Developing and implementing procedures in the study.They will be training and guiding other members of the study.

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