Overview
We are seeking a dynamic and detail-oriented Patient Recruitment Coordinator to join our clinical research team. Applicants must be bilingual in English and Spanish (spoken and written). In this vital role, you will lead efforts to identify, engage, and enroll suitable participants for our clinical trials, ensuring compliance with regulatory standards and ethical guidelines. Your proactive approach and excellent communication skills will help accelerate research timelines while maintaining the highest standards of patient care and data integrity. This paid position offers an exciting opportunity to contribute to groundbreaking healthcare advancements in a fast-paced research environment.
Duties
- Develop and implement patient recruitment strategies aligned with study protocols, including outreach through community engagement, digital platforms, and healthcare provider networks.
- Screen potential participants by reviewing medical records, conducting interviews, and assessing eligibility based on inclusion/exclusion criteria.
- Coordinate patient appointments for screenings, blood sampling, and follow-up visits while ensuring adherence to clinical ethical guidelines and HIPAA regulations.
- Maintain accurate documentation of recruitment activities, patient interactions, and screening outcomes in electronic medical record (EMR) systems.
- Monitor patient progress throughout the study, providing support and addressing concerns to enhance retention rates.
- Review clinical documentation for accuracy, completeness, and compliance with FDA regulations and ICH GCP standards.
- Collaborate with project managers and clinical staff to ensure timely data collection, adherence to clinical trials management protocols, and quality assurance standards.
Qualifications
- Effective communication skills to liaise with patients, healthcare providers, regulatory bodies, and internal teamsProven experience in clinical research settings with a focus on patient recruitment or clinical trial coordination.
- Strong knowledge of medical terminology, clinical development processes, and healthcare compliance standards such as HIPAA and FDA regulations.
- Excellent analysis skills combined with project management experience in healthcare or research projects.
- Ability to review complex documentation accurately while adhering to clinical quality assurance standards.
- Knowledge of blood sampling procedures, clinical laboratory practices, and research setting experience is highly desirable.
Join us in advancing medical science by recruiting dedicated participants who help shape the future of healthcare! This role offers a unique chance to be at the forefront of clinical innovation while developing your expertise in research compliance, project management, and patient engagement within a supportive team environment.
Pay: $19.00 - $21.00 per hour
Benefits:
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Experience:
- customer service: 1 year (Required)
Language:
- English and Spanish (Required)
Ability to Commute:
- Tampa, FL 33607 (Required)
Work Location: In person
