Full-Time

Clinical Research Participant Specialist

University of Miami

University of Miami

Research university in Coral Gables, FL

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA

Hybrid

Hybrid work arrangement in Miami.

Bachelor's

Category
Biology & Biotech (1)
Required Skills
Microsoft Office
R
Social Media
Word/Pages/Docs
HIPAA
Excel/Numbers/Sheets
Microsoft Outlook
PowerPoint/Keynote/Slides

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Requirements
  • A bachelor's degree is required, preferably in Psychology, Biology, Public Health, Neuroscience, or a related field.
  • No previous experience is required.
  • Strong organizational and communication skills are required.
  • The ability to work independently and in a team-based research environment is required.
  • Experience with REDCap data entry and management is preferred.
  • Familiarity with SPSS, RStudio, or other statistical software is preferred.
  • Experience interacting with diverse populations in community or clinical settings is preferred.
  • Proficiency in Microsoft Office Suite, including Word, Excel, PowerPoint, and Outlook, is preferred.
Responsibilities
  • Assist with the design and implementation of recruiting strategies for clinical studies and trials.
  • Source and recruit study participants using databases, social media, hospitals, mental health clinics, shelter programs, and other referral sources.
  • Prescreen and evaluate candidates for study participation.
  • Provide analytical and well-documented recruiting reports to leadership.
  • Act as a point of contact and build client relationships during the prescreen process.
  • Market clinical trials to the community and participate in community outreach events to promote study awareness.
  • Schedule and conduct marketing presentations for referral sources.
  • Understand Phase I through Phase IV clinical protocols and develop recruitment programs accordingly.
  • Act as a primary liaison between referral sources and the organization.
  • Complete demographic, intake, database consent, release-of-information, and other required forms during initial evaluations, review program criteria, and maintain the patient database.
  • Visit hospitals, clinics, and other referral sources to market studies and conduct face-to-face screenings and assessments to determine eligibility.
  • Communicate with family members or other persons involved in participants' care.
  • Design and develop client education materials as needed.
  • Attend interdisciplinary treatment-team meetings as needed.
  • Recruit, screen, consent, and enroll eligible participants according to Institutional Review Board-approved study protocols.
  • Conduct structured research visits, including questionnaire administration, cognitive assessments, and biometric measurements, as required by protocol.
  • Schedule and coordinate baseline, follow-up, virtual, and in-person participant visits.
  • Maintain consistent communication with participants to support retention and adherence to study procedures.
  • Serve as a point of contact for participants regarding study procedures, scheduling, and general inquiries.
  • Assist with community outreach efforts supporting recruitment goals.
  • Collect, document, and enter study data accurately into REDCap and other approved data-management systems.
  • Ensure data completeness, quality control, and protocol compliance.
  • Monitor recruitment metrics, retention rates, and study milestones.
  • Support data cleaning and preparation of datasets for analysis.
  • Maintain confidentiality and HIPAA compliance when handling participant information.
  • Prepare and maintain regulatory documents, including regulatory binders, consent forms, and study logs.
  • Support Institutional Review Board submissions, modifications, and continuing reviews as directed by study leadership.
  • Maintain study supply inventory and assist with ordering and organizing research materials.
  • Prepare documentation for monitoring visits and audits.
  • Coordinate specimen-collection logistics, including blood, saliva, actigraphy devices, and sleep-monitoring equipment when applicable.
  • Participate in weekly study meetings and team trainings.
  • Collaborate with the Principal Investigator, project manager, and research team to execute study goals on time.
  • Assist with preparing abstracts, posters, and presentations as opportunities arise.
  • Engage in professional development related to clinical research and sleep/circadian science.
  • Attend approved field-related conferences, seminars, and trainings.
  • Adhere to University and unit-level policies and procedures and safeguard University assets.
Desired Qualifications
  • Prior laboratory or clinical research experience is preferred.
  • Experience interacting with diverse populations in community or clinical settings is preferred.

The University of Miami is a private research university focused on education, discovery, and service, with undergraduate, graduate, and professional programs.

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