Job Overview
We are seeking a dynamic and detail-oriented Clinical Research Recruiter to join our team and drive the success of our clinical trials. In this vital role, you will be responsible for identifying, screening, and enrolling suitable participants for various clinical studies. Your expertise will ensure that recruitment processes align with regulatory standards and study protocols, facilitating smooth trial operations. This position offers an exciting opportunity to contribute to groundbreaking medical research while working in a fast-paced, collaborative environment dedicated to advancing healthcare.
Duties
- Develop and implement effective recruitment strategies to identify eligible participants for clinical trials, ensuring adherence to protocol specifications and regulatory guidelines.
- Screen potential candidates through interviews, medical record reviews, and assessments of medical history, ensuring compliance with inclusion/exclusion criteria.
- Coordinate with clinical staff to monitor patient progress, collect necessary documentation, and facilitate participant engagement throughout the trial lifecycle.
- Maintain accurate and comprehensive documentation review processes, including consent forms, medical histories, and compliance records in accordance with FDA regulations and ICH GCP standards.
- Manage data collection and entry into electronic Medical Record (EMR) systems while ensuring data integrity and confidentiality in compliance with HIPAA guidelines.
- Conduct patient monitoring activities such as vital signs assessment, blood sampling (phlebotomy), and recording clinical laboratory results following protocol procedures.
- Collaborate with research teams to ensure adherence to CDISC standards for data management and reporting during all phases of clinical development.
Skills
- Proven supervising experience in clinical research or related healthcare settings.
- Strong knowledge of clinical trials management, including patient recruitment, documentation review, and compliance management.
- Familiarity with medical terminology, blood sampling techniques (phlebotomy), vital signs measurement, and clinical laboratory procedures.
- Proficiency with statistical software and data analysis tools used in research environments.
- Deep understanding of FDA regulations, ICH GCP guidelines, HIPAA compliance, and CDISC standards for data collection.
- Experience working with EMR systems and clinical development processes across various phases of trials.
- Excellent communication skills for engaging patients effectively while maintaining professionalism in all interactions.
- Ability to review complex documentation accurately while maintaining meticulous records aligned with regulatory standards.
- Knowledge of research methodologies including patient monitoring techniques and clinical laboratory experience is highly desirable. Join us to be part of a dedicated team committed to advancing medical science through innovative research! This paid position offers an enriching environment where your expertise can make a meaningful difference in healthcare outcomes worldwide.
Work Location: In person
