Clinical Research Participant Specialist
University of Miami
This job at a glance
- Who can apply
- New grads, no experience needed · Bachelor's degree
- Must know
- Patient careRecruitingSocial mediaMarketingStakeholder management
- Work
- On-site in Miami
- Pay
- Not stated by the employer.
- Skill demand
- Patient care76%Recruiting37%Marketing7%Social media2%of 99 similar entry-level jobs posted in the US this week
- Listed
- Oct 30, 2026 · still open
Sign in free to see which of these skills your resume already shows.
About the Role
The University of Miami/UHealth Department of Psychiatry has an opportunity for a full-time Clinical Research Participant Specialist to work in Miami, FL. This role supports participant outreach, recruitment, enrollment, and study visit coordination on the University of Miami Medical Campus.
Key Responsibilities
- Assists in community outreach, recruitment, and enrollment of participants for clinical studies/trials.
- Assists with the design and implementation of overall recruiting strategy for clinical studies/trials.
- Sources and recruits study participants 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 the prescreen process.
- Markets clinical trials to the 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) and associated study specifications.
- Develops effective client recruitment programs.
- 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.).
- Reviews the criteria for the programs.
- Updates and maintains the patient database with required information.
- Visits appropriate referral sources (hospitals, clinics, etc.) to market clinical studies/trials.
- 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 the interdisciplinary treatment team.
- Attends field-related conferences/seminars/trainings.
- Supports participant recruitment, prescreening, enrollment, scheduling, and follow-up in accordance with approved research protocols.
- Conducts telephone and in-person interviews and assessments.
- Completes participant intakes, consent-related documentation, and data collection.
- Maintains 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.
- Maintains organized study files and binders.
- Participates in community outreach and recruitment activities to support participant engagement and retention.
- Communicates effectively with multidisciplinary research teams and community partners.
- Adheres to university policies, confidentiality, and ethical standards.
Requirements & Tech Stack
- Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands.
- Teamwork: Ability to work collaboratively with others and contribute to a team environment.
- Technical Proficiency: Skilled in using office software, technology, and relevant computer applications.
- Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders.
Qualifications
- Bachelor’s degree in a relevant field required.
- No previous experience required.