Clinical Research Coordinator 1

Posted Yesterday
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Miami, FL, USA
In-Office
Junior
Other
The Role
Entry-level Clinical Research Coordinator responsible for participant prescreening, coordinating routine study activities, data collection, regulatory binder maintenance, reporting adverse events, and following research protocols and compliance standards under supervision.
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The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Clinical Research Coordinator 1 to work at the UHealth campus in Miami, Fl. 

CORE JOB SUMMARY

The Clinical Research Coordinator 1 serves as an entry level clinical research professional that has a basic foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. This role exhibits increased learned skills and flexibility in performing duties and assumes responsibility for simple clinical research protocols and timelines.

CORE JOB FUNCTIONS

  • Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols. Maintains enrollment procedures according to the protocol.

  • Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation.

  • Performs moderate to complex research tests/ experiments and adapts procedures for quality improvement under supervision.

  • Understands and follows technical instructions for operating clinical research equipment, problem solves when operational failures occur.

  • Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants.

  • Addresses adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study.

  • Identifies, reports, and helps problem solve protocol deviations and unanticipated occurrences.

  • Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.

  • Knows the contents and maintenance of study-specific clinical research regulatory binders.

  • Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.

  • Adheres to University and unit-level policies and procedures and safeguards University assets.

  • This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.

CORE QUALIFICATIONS
Education:
Bachelor’s degree in relevant field required
Experience:
Minimum 1 year 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.

The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.

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.

The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.

Job Status:

Full time

Employee Type:

Staff

Skills Required

  • Bachelor's degree in relevant field
  • Minimum 1 year of relevant experience
  • Ability to perform chart review/prescreening and coordinate clinical research protocols
  • Knowledge of study-specific clinical research regulatory binders
  • Ability to observe, report, and assist in addressing adverse events per protocol
  • Skill in completing assignments accurately with attention to detail
  • Ability to analyze, organize, and prioritize work under pressure and meet deadlines
  • Ability to process and handle confidential information with discretion
  • Ability to work evenings, nights, and weekends as necessary
  • Maintain requisite skills and mandatory training in safety, responsible conduct of research, and research competencies
  • Ability to work independently and/or in a collaborative environment
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The Company
HQ: Miami, FL
17,000 Employees

What We Do

The University of Miami is a leading research university dedicated to transforming lives through education, research, innovation, and service.

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