Clinical Research Coordinator - Phase One
Job location: Miami, FL
Employment Type: Full-time
Posted data: 2019-01-11
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The Clinical Research Coordinator (CRC) will assist the Principal Investigator in the conduct all aspects of the clinical trial, including regulatory tasks, under the direct supervision of the Principal Investigator, and Clinical Research Manager. The CRC provides operational and administrative support in the management of patients accrued to multiple research protocols to assure subjects’ safety and regulatory compliance. The CRC is responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, Standard Operating Procedures and all applicable regulations and guidelines and ensuring effective data flow associated with research protocols. The CRC is critical to ensuring the safety of patients enrolled on a clinical trial. Patient duties include but are not limited to:
I. Meeting with the patient in clinic and providing information on the specific clinical trial; answering the patient questions and facilitating the informed consent process
II. Providing the patient a point of contact for all clinical trial questions or concerns
III. Being available and present in clinic and in the Chemotherapy Treatment Unit when the patient is dosed
IV. Meeting the patient in clinic for all visits during treatment and follow up to ensure the patient is fully informed and any questions or concerns addressed
V. Being available in the clinic to the physician and the patient to ensure protocol compliance and source data is documented appropriately and according to Good Clinical Practice
VI. Attending clinic at the time of the patient visit to ensure all adverse event documentation and concomitant medication information is documented according to the protocol requirements
VII. Ensuring all patient protocol appointments are scheduled as required.
- Bachelor’s Degree in relevant field required.
- Experience:Minimum 2 years of relevant experience.
- Knowledge, Skills and Attitudes: Skill in completing assignments accurately and with attention to detail. Ability to analyze, organize and prioritize work under pressure while meeting deadlines. Ability to process and handle confidential information with discretion.Ability to work evenings, nights, and weekends as necessary. Commitment to the University’s core values. Ability to work independently and/or in a collaborative environment.
UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.
Patient safety is a top priority. As a result, during the Influenza ("the flu") season (September through April), the University of Miami School of Medicine requires all employees who provide ongoing services to patients, work in a location (all Hospitals and clinics) where patient care is provided, or work in patient care or clinical care areas, to have an annual influenza vaccination. Failure to meet this requirement will result in rescinding or termination of employment.
The University of Miami is an Equal Opportunity Employer - Females/Minorities/Protected Veterans/Individuals with Disabilities are encouraged to apply. Applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here for additional information.Job Status:Full timeEmployee Type:StaffPay Grade:r6