Patient Recruitment Specialist

Patient Recruitment Specialist Hi Tech and Global Research Coral Gables, FL Job Details Part-time | Full-time | Contract From $20 an hour 1 day ago Qualifications Data analysis skills HIPAA Research Data collection Medical terminology Full Job Description Job Summary We are seeking a dynamic and motivated Patient Recruitment Specialist to join our clinical research team. In this vital role, you will lead efforts to identify, engage, and enroll suitable participants for various clinical trials. Your energetic approach and attention to detail will ensure the successful recruitment of diverse patient populations, facilitating groundbreaking medical research. This paid position offers an exciting opportunity to contribute directly to advancements in healthcare while developing your expertise in clinical trials management and patient engagement. Duties Develop and implement strategic patient recruitment plans aligned with study protocols and regulatory requirements. Identify potential participants through outreach activities, community engagement, and other channels. Screen prospective patients by reviewing medical histories, conducting interviews, and verifying eligibility criteria based on clinical trial protocols. Coordinate with healthcare providers, clinics, and community organizations to facilitate patient referrals and increase trial awareness. Maintain accurate documentation of recruitment activities, including consent forms, screening logs, and communication records in compliance with HIPAA and FDA regulations. Monitor patient progress throughout the trial, ensuring adherence to study protocols and managing retention efforts effectively. Collaborate with the clinical team to review data collection processes, ensure compliance with ICH GCP standards, and support quality assurance initiatives. Qualifications Proven supervising experience in a clinical or research setting with a focus on patient engagement or recruitment. Strong knowledge of clinical trials management, including familiarity with FDA regulations, ICH GCP guidelines, and CDISC standards for data management. Excellent understanding of medical terminology, blood sampling techniques such as phlebotomy, vital signs measurement, and patient monitoring procedures. Experience working with EMR systems, clinical laboratories, and data collection tools used in research environments. Ability to review complex documentation accurately while ensuring compliance with HIPAA and other privacy standards. Demonstrated analysis skills for assessing recruitment metrics and optimizing strategies accordingly. Certification in Good Clinical Practice (GCP), ICH GCP certificate from a recognized issuer for CA or equivalent is preferred. Knowledge of clinical development processes, research methodologies, and clinical laboratory procedures is highly desirable. Join us to make a meaningful impact on healthcare innovation! This role offers a vibrant environment where your proactive approach will help advance vital medical research while honing your skills in clinical trials management and patient care compliance.

Pay:

From $20.00 per hour Expected hours: 15.0 - 25.0 per week

Work Location:

In person