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Clinical Research Coordinator 2
4 weeks ago
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.
CORE JOB FUNCTIONS
Assists in participant recruitment and retention activities and assists in screening potential study participants for eligibility. Performs study procedures, routine tests, data collection/recording, and daily operations of moderate risk clinical research protocols. Collects, processes, packs, and ships specimens according to protocol, applicable standards and regulations. Maintains study binders and filings according to protocol requirements, UM and department policy. Distributes study drug materials according to practice standards and clinical credentials as delegated by the Principal Investigator. Monitors, documents, reports, and follows-up on study unanticipated/adverse events and protocol deviations. Assists in implementing protocol amendments under direct supervision of the Principal Investigator. 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. Learns the research team and assists with communications/interactions with sponsor, data coordinating centers, compliance monitors, collaborators, investigators' academic administrative personnel, and departments. 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. Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies. 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
Certification and Licensing:
Not Applicable
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.
DEPARTMENT ADDENDUM
Department Specific Functions
The Clinical Research Coordinator 2 will support recruitment and data collection activities under the direction of the principal investigator (Sara St George PhD). Dr. St George's program of research is focused on promoting health, prevent chronic disease, and foster positive relationships among Hispanic families by developing, evaluating, and disseminating evidence-based multigenerational digital lifestyle interventions.
The position is full-time, with remote and in-person presence at the Miller School of Medicine at the Medical Campus of University of Miami.
Ongoing projects in the lab which the manager would support are:
- Healthy Juntos: This is an efficacy trial of a family-based digital obesity prevention intervention ("Healthy Juntos") for Hispanic parents and their 12–15-year-old adolescents. Healthy Juntos is a web-based application that includes eleven modules of content for parents and adolescents delivered over six months. Eligible families who chose to participate in the study will be randomly assigned to either use our family health app or receive free digital health resources.
- Con Cariño Abuelita: This is a pilot study of a multi-generational family-based digital cancer and obesity prevention intervention ("Con Cariño Abuelita") for Hispanic cancer survivors and their daughters/daughters in-law. Con Cariño Abuelita is a web-based application that includes eight modules of content for over three months. Eligible families who chose to participate in the study will be randomly assigned to either use our family health app or receive free digital health resources.
Primary duties and responsibilities:
- Overall study coordination across the lab (e.g., achieving recruitment milestones, assisting with progress reports, and coordinating team members to ensure timely completion of projects).
- Attending weekly lab meetings and project-specific meetings and assisting with preparing agendas and summarizing meeting minutes.
- Holding weekly group or individual staff meetings to provide overall supervision to recruitment and data collection team members.
- Attending/leading meetings with community partners for ongoing projects or building new relationships with new community partners.
- Assisting with "root cause analysis" discussions with team members if non-compliance occurs and developing corrective action plans as needed.
- Assisting with other team members' recruitment and retention efforts (e.g., problem solving recruitment barriers, creating actionable recruitment plans, etc.).
- Supporting collaborations with other research teams, schools, universities, partners, or investigators.
Education:
Bachelor's Degree in relevant field
Master's degree (preferred)
Certification and Licensing:
Not Applicable
Experience:
Minimum 2 year of relevant experience
Knowledge, Skills and Attitudes:
- Skill in completing assignments accurately and with attention to detail.
- Ability to document and synthesize study reports.
- 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.
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 timeEmployee Type:
StaffPay Grade:
A9-
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