U

University of Miami

Research university in Coral Gables, FL

Clinical Research Participant Specialist

Full-Time
No salary listed
Mid
Bachelor's
Miami, FL, USA
In PersonLocal travel is involved.
Academic & Institutional ResearchMedical Research
Company Does Not Provide H1B Sponsorship

About the job

Requirements
  • A bachelor’s degree in a relevant field.
  • At least one year of related experience.
  • Ability to maintain effective interpersonal relationships.
  • Proficiency in computer software, including 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.
  • Ability to interact with a variety of audiences.
  • Experience in recruitment, phone scheduling, and participant outreach.
  • Strong verbal communication, interviewing, and writing skills.
  • Excellent time management and organizational skills.
  • Experience compiling data, maintaining confidentiality, and working as a reliable team member.
  • Ability to accurately and carefully document all study participant interactions in a timely manner.
  • Ability to complete service plans and participant evaluations as directed.
  • Creativity, flexibility, sound judgment, and the ability to take initiative.
  • Experience or willingness to undergo training to perform phlebotomy.
  • Commitment to the University’s core values.
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 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 outreach events to promote study awareness.
  • Schedule and conduct marketing presentations for referral sources.
  • Understand Phase I through Phase IV clinical protocols and develop effective client 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 referral sources to market clinical studies and conduct face-to-face screenings and assessments to determine eligibility; communicate with family members or others involved in participants’ care.
  • Design and develop client education materials as needed.
  • Attend meetings with interdisciplinary treatment teams as needed.
  • Attend field-related conferences, seminars, and trainings as approved by the supervisor.
  • Participate in implementing policies and procedures to accomplish program goals.
  • Participate in outreach, recruitment, enrollment, and retention activities.
  • Participate in community events and other activities to increase program awareness.
  • Help design and implement culturally appropriate recruitment, enrollment, and retention strategies.
  • Recruit, enroll, and retain study participants, including obtaining informed consent and conducting interviews and questionnaires according to detailed procedures and guidelines.
  • Schedule appointments for program participants.
  • Maintain effective phone and email communication with potential and enrolled participants to support study goals and objectives.
  • Conduct basic examinations, including height, weight, automated blood pressure readings, and hip-waist ratios, according to detailed procedures and guidelines.
  • Maintain logs and progress reports tracking prospective and enrolled participants and follow-up program activities.
  • Oversee procedures for collecting, processing, and shipping biospecimens to the designated biobank.
  • Assist with maintaining and calibrating study equipment.
  • Help develop forms for collecting and summarizing data as needed.
  • Enter data and assist with creating and maintaining databases.
  • Verify the accuracy, integrity, and consistency of research data and participate in data quality control.
  • Assist with institutional review board processes, including reporting safety or study deviations and initiating modifications to study procedures.
  • Conduct phlebotomy procedures as needed.
  • Participate in ongoing University of Miami and research-related training.
  • Maintain all required research certifications.
  • Assist with other assigned research and administrative activities.
  • Travel locally as required.
Desired Qualifications
  • Prior experience conducting research recruitment activities.
  • Bilingual proficiency in English and Spanish.
  • Phlebotomy certification.

About the company

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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