Full-Time

Clinical Research Participant Specialist

University of Miami

University of Miami

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA

In Person

Category
Biology & Biotech (2)
,
Required Skills
Social Media
Requirements
  • Bachelor’s degree in relevant field
  • No Experience Required
  • Ability to communicate effectively in both oral and written form
  • 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
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 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
  • Supports participant recruitment, prescreening, enrollment, scheduling, and follow-up in accordance with approved research protocols
  • Conducts telephone and in-person interviews and assessments at UM/Jackson HIV Clinic, Converge Miami, and the Clinical Research Building (CRB)
  • Completes participant intakes, consent-related documentation, data collection, and database updates, maintaining accurate study records
  • Serves as a primary point of contact for participants, providing study information, appointment reminders, and follow-up communication
  • Coordinates study visits, prepares correspondence, manages phone inquiries, and maintains organized study files and binders
  • Participate in community outreach and recruitment activities to support participant engagement and retention
  • Communicates effectively with multidisciplinary research teams and community partners while adhering to university policies, confidentiality, and ethical standards
  • 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

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