Patient Recruitment Specialist

Job Summary
We are seeking a dynamic and detail-oriented Clinical Research Patient Recruitment Specialist to join our clinical research team. In this pivotal role, you will drive the success of clinical trials by identifying, engaging, and enrolling suitable participants in accordance with regulatory standards and ethical guidelines. Your energetic approach and excellent communication skills will ensure a seamless recruitment process, contributing to groundbreaking healthcare advancements. This paid position offers an exciting opportunity to be at the forefront of clinical development while working within a collaborative, compliance-driven environment.

Duties

• Develop and implement innovative patient recruitment strategies tailored to specific clinical trials, ensuring timely enrollment of eligible participants
• Screen potential participants through detailed review of medical histories, documentation, and adherence to inclusion/exclusion criteria
• Conduct patient monitoring activities, including vital signs measurement, blood sampling (phlebotomy), and assessment of health status in compliance with clinical protocols
• Maintain accurate documentation review and data collection in accordance with Good Clinical Practice (GCP), FDA regulations, and CDISC standards
• Collaborate with clinical staff to ensure adherence to ethical guidelines, healthcare compliance, and research project management protocols
• Utilize electronic medical record (EMR) systems and statistical software for data management and reporting purposes
• Supervise junior team members or research assistants involved in patient outreach or data collection activities

Qualifications

• Proven supervising experience within a clinical research or healthcare setting, demonstrating leadership capabilities
• Strong knowledge of medical terminology, clinical laboratory procedures, and blood sampling techniques (phlebotomy)
• Familiarity with clinical research methods, compliance standards such as HIPAA, ICH GCP guidelines, and FDA regulations governing clinical trials
• Experience reviewing documentation for accuracy and completeness; adept at data management and analysis using statistical software
• Proficiency in Microsoft Office suite (Word, Excel, PowerPoint) and EMR systems for efficient documentation and reporting
• Certification in ICH Good Clinical Practice (GCP) from a recognized issuer; valid CA certification preferred
• Background in healthcare compliance management, clinical quality assurance standards, and research project oversight
• Knowledge of clinical ethical guidelines, research setting experience, and project management skills in healthcare environments
• Ability to monitor patient vital signs accurately; experience with blood sampling (phlebotomy) is highly desirable
• Excellent communication skills to effectively engage diverse participant populations while maintaining confidentiality under HIPAA regulations

Join us to make a meaningful impact on healthcare innovation by recruiting the right participants for vital clinical trials. Your expertise will help shape the future of medicine while working in a vibrant environment committed to excellence in research.

Pay: $500.00 - $1,500.00 per week

Benefits:

• Flexible schedule

Work Location: Remote