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Clinical Research Coordinator 2 Jobs

Company

University of Miami

Address Miami, FL, United States
Employment type FULL_TIME
Salary
Category Higher Education
Expires 2023-09-05
Posted at 9 months ago
Job Description
Current Employees:


If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position using the Career worklet, please review this tip sheet.


The Department of Pediatrics- Infectious Disease has a great opportunity for a Clinical Research Coordinator 2. The Clinical Research Coordinator 2 serves as a mid-level clinical research professional that assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. This role assists in the day-to-day operations of clinical research protocol implementation, and carries out study coordination duties from protocol initiation to study close-out according to regulatory/sponsor guidelines. The incumbent works closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols, help with study-related administrative tasks, facilitate across-the-board flow of information, and coordinate study activities and personnel.


  • Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
  • Collects, processes, packs, and ships specimens according to protocol, applicable standards and regulations.
  • Assist principal investigators, project managers in coordinating Federal and/or industry-sponsored research studies.
  • Assists in administrative tasks of study personnel including orientation, documenting core competencies, certification mandates, safety/responsible conduct of research education, and performance reviews.
  • Adheres to cultural competency guidelines; implements strategies to meet study participants’ needs for language translation, health literacy, etc.
  • Assists with study orientation and protocol related in-services to research team and clinical staff.
  • Monitors protocol implementation and study progress; keeps investigators fully apprised of study progress; submits progress reports according to established schedule.
  • Distributes study drug materials according to practice standards and clinical credentials as delegated by the Principal Investigator.
  • Adheres to University and unit-level policies and procedures and safeguards University assets.
  • Assists in participant recruitment and retention activities, and assists in screening potential study participants for eligibility.
  • Monitors, documents, reports, and follows-up on study unanticipated/adverse events and protocol deviations.
  • Maintains study binders and filings according to protocol requirements, UM and department policy.
  • Assists in implementing protocol amendments under direct supervision of the Principal Investigator.
  • Performs study procedures, routine tests, data collection/recording, and daily operations of moderate risk clinical research protocols.
  • Learns the research team and assists with communications/interactions with sponsor, data coordinating centers, compliance monitors, collaborators, investigators’ academic administrative personnel, and departments.
  • Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.


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.


MINIMUM QUALIFICATIONS:


  • Bachelor’s degree in relevant field required.
  • Commitment to the University’s core values.
  • Ability to work evenings, nights, and weekends as necessary.
  • Ability to work independently and/or in a collaborative environment.
  • Bilingual English and Spanish preferred.
  • Ability to process and handle confidential information with discretion.
  • Minimum 2 years of relevant experience.
  • Skill in completing assignments accurately and with attention to detail.
  • Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
  • Ability to work with children and their caregivers.


Any appropriate combination of relevant education, experience and/or certifications may be considered.


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.


Patient safety is a top priority. As a result, during the Influenza ("the flu") season (September through April), the University Of Miami Miller 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 time


Employee Type:


Staff


Pay Grade:


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