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  3. Clinical Research Participant Specialist
UOMUOMUS logo

Clinical Research Participant Specialist

UOMUOMUS·Coral Gables, Florida

OtherFull TimeOn Site0-2 yrsPosted 12 days ago
Practice for this role

Clinical Research Participant Specialist

About the role

The Clinical Research Participant Specialist assists in the recruitment, enrollment, and retention of participants for clinical studies through community outreach and marketing. They also conduct clinical intakes, assessments, and basic examinations while maintaining accurate research data and participant databases.

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, please review this tip sheet. Clinical Research Participant Specialist The University of Miami/UHealth Hussman Institute has an exciting opportunity for a Full Time, Clinical Research Participant Specialist to work in Miami.

Core

Job

Summary: The Clinical Research Participant Specialist assists in community outreach, recruitment, and enrollment of participants for clinical studies/trials. Moreover, the Clinical Research Participant Specialist schedules assessments, completes clinical intakes and assessments, conducts in-person and telephone interviews, and markets clinical studies/trials.

Core

Responsibilities: Assists with the design and implementation of overall recruiting strategy for clinical studies/trials. Sources and recruits study participants by using databases, social media, hospitals, mental health clinics, shelter programs, etc. Prescreens and evaluates candidates for study participation. Provides analytical and well-documented recruiting reports to leadership. Acts as a point of contact and builds influential client relationships during prescreen process. Markets clinical trials to community and participates in community outreach events to promote study awareness. Schedules and conducts marketing presentations to various referral sources. Understands clinical protocols (i.e., Phase I to Phase IV), associated study specifications and develops effective client recruitment programs accordingly. Acts as a primary liaison between referral sources and the organization.

Completes required forms during the initial evaluation: demographic form, intake form, database consent form, releases of information, etc. and reviews the criteria for the programs. Updates and maintain patient database with required information. Visits appropriate referral sources (i.e., hospitals, clinics, etc.) to market clinical studies/trials and conducts face-to-face screenings and assessments to determine eligibility; communicates with family or persons involved in participant’s care. Designs and develops client education materials as needed. Attends and participates in meetings with interdisciplinary treatment team as needed. Attends field related conferences/seminars/trainings as approved by supervisor. Adheres to University and unit-level policies and procedures and safeguards University assets.

Department Specific Functions

Participates in the implementation of policies and procedures to accomplish program goals. Participates in outreach, recruitment, enrollment, and retention activities. Participates in community events and other activities to increase program awareness. Helps design and implement culturally appropriate recruitment, enrollment, and retention strategies. Recruits, enrolls and retains participants into the study including obtaining informed consent, conducting interviews and questionnaire completion with research participants according to detailed procedures and guidelines. Participates in the scheduling of appointments for program participants. Maintains effective lines of communications (phone/emails) with potential and enrolled participants to ensure adherence to study goals and objectives are met. Conducts basic examinations such us heigh, weight, automated blood pressure reading, and hip waist ratios according to detailed procedures and guidelines. Maintains logs/progress reports to track prospective and enrolled participants as well as participants for follow up program activities. Oversees procedures for collecting, processing, and shipping biospecimens to the designated biobank. Assists on the maintenance and calibration of study equipment. Helps develop forms for collecting/summarizing data as needed. Enters data and assists with the creation and maintenance of databases. Verifies accuracy, integrity and consistency of research data and participates in data quality control. Provides assistance with IRB processes (e.g., abiding by requirement for reporting safety or study deviations, initiating modifications to study procedures, etc.). Conducts phlebotomy procedures as needed. Participates in ongoing UM and research related trainings. Maintains all required research certifications. Assists with other research and administrative activities as assigned. Local travel involved. Bilingual in (English and Spanish) is preferred. Phlebotomy certification is preferred. 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: Bachelor’s degree in relevant field. Minimum one year of related experience required Ability to maintain effective interpersonal relationships. Proficiency in computer software (i.e. Microsoft Office) 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. Ablility to interact with a variety of audiences. Recruitment, phone scheduling and participant outreach experience. Prior experience conducting research recruitment activities is preferred. Strong verbal communication, interviewing, and writing skills. Excellent time management and organizational skills. Compiling data, maintaining confidentiality, and working as a reliable team member. Accurately, and carefully documenting all study participant interactions in a timely fashion. Complete service plans and participant evaluations as directed. Creativity, flexibility, sound judgment, and ability to take initiative. Experience or willingness to undergo training to perform phlebotomy. Commitment to the University’s core values. 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

Requirements

Candidates must hold a bachelor's degree in a relevant field and possess at least one year of related experience. Strong interpersonal, organizational, and communication skills are required, along with the ability to handle confidential information and work flexible hours.

  • bachelor degree
  • Phlebotomy
  • Microsoft Office
  • Marketing
  • Communication skills
  • Interpersonal skills
  • Time management
  • Data entry
  • Community outreach
  • Clinical research
  • Informed consent
  • Clinical intake
  • Participant recruitment
  • Data quality control
  • Patient database management
  • IRB processes

Benefits

  • Medical
  • Dental
  • Tuition remission

Posting details

Employment type
Other, Full Time
Work arrangement
On Site
Experience
0-2 yrs
Location
Coral Gables, Florida
Posted
Aug 27, 2026
Application
Employer website
UOMUOMUS logo

Hiring organization

UOMUOMUS

UOMUOMUS is hiring in Coral Gables, Florida. It operates in medical practices. Team size: 11-50 employees. Headquarters: Coral Gables, Florida. This opening is listed as other, full_time.

IndustryMedical Practices
Size11-50 employees
HQCoral Gables, Florida
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Market context

Florida clinical research roles stay competitive

In Florida, Clinical Research Participant Specialist roles are typically tied to active study recruitment and participant support, so demand often follows the pace of local research programs and clinical trial activity. These positions are competitive because employers look for a relevant bachelor’s degree, at least one year of related experience, strong Microsoft Office skills, and flexibility for evenings and weekends. Review the AI-summarized requirements and benefits here to save research time, then tailor your application to show participant-facing experience and schedule availability.

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