Research Support Specialist (N) at University of Miami in Miami, Florida

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 University of Miami is currently seeking a Research Support Specialist to work at Soffer Clinical Research Center in Miami. The incumbent performs a variety of duties involved in the collection, compilation, and documentation of research data related to the assigned research studies. He/she also assists with the implementation of daily study activities and provides statistical support to these activities.



CORE JOB FUNCTIONS
1. Researches, collects, analyzes, and synthesizes data and maintains databases.
2. Conducts quality assurance checks, reports on the status of research activities, and submits monthly activity logs for protocol.
3. Organizes and coordinates community working group meetings for protocol activities.
4. Serves as the primary point of contact for community partners and supervises and oversees research data collection at protocol venues in the community.
5. Reviews study progress, identifies areas of opportunity, and recommends solutions.
6. Prepares and updates study research procedures manuals.
7. Assists with the preparation of grant proposals by processing regulatory documents for all institutions and offices involved.
8. Contributes to the publication and presentation of significant results and writes and edits material for publication and presentation.
9. Maintains research files and responds to phone calls on the research study phone line.
10. Adheres to University and unit-level policies and procedures and safeguards University assets.



Department Specific Functions



The Research Support Specialist serves as an entry-level clinical research professional who has a basic foundation in clinical research through assigned responsibilities in patient screening and enrollment, data management, and implementing research protocols. This role exhibits increased learned skills and flexibility in performing duties and assumes responsibility for scientific and research support.


1. Enrolling new patients to participate in clinical research.
2. Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols. Maintains enrollment procedures according to the protocol.
3. Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, scheduling appointments and study visits, meeting scheduling, and project evaluation.
4. Performs moderate research tasks and adapts procedures for quality improvement under supervision.
5. Understands and follows technical instructions for operating clinical research equipment, and problem-solving when operational failures occur.
6. Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants.
7. Addresses adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study.
8. Identifies, reports, and helps solve problems in protocol deviations and unanticipated occurrences.
9. Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
10. Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
11. Prepare monthly progress reports and annual self-evaluation of performance. Adheres to Department-Specific policies and procedures and safeguards Department 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:



CITI Program: Human Subject Research, Group 1: Biomedical Researchers (HSR), and Conflict of Interest (COI) preferred.



Experience:



Minimum 2 years of relevant experience


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:

Part time



Employee Type:

Staff



Pay Grade:

A6