Patient Recruitment Specialist

Benefits

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
• •3 more items(s)

Responsibilities

• •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
• •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
• •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
• •8 more items(s)