Clinical Trials Patients Recruiter Advanced Research Center, Inc. - 2.7 Anaheim, CA Job Details Temporary | Part-time | Full-time | Contract $20 - $27 an hour 17 hours ago Benefits Health insurance Paid time off Flexible schedule Retirement plan Qualifications Statistical software Statistics Sales analytics & reporting tools Sales HIPAA Patient interaction Medical terminology Full Job Description Job Summary We are seeking a dynamic and dedicated Clinical Trials Patients Recruiter to join our innovative research team. In this vital role, you will spearhead patient recruitment efforts for clinical trials, ensuring timely enrollment of qualified participants while maintaining compliance with regulatory standards. Your proactive approach and excellent communication skills will help bridge the gap between research objectives and patient needs, contributing to groundbreaking medical advancements. This paid position offers an exciting opportunity to be at the forefront of clinical research, making a meaningful impact on healthcare development. Duties Develop and implement effective patient recruitment strategies aligned with study protocols and regulatory guidelines. Conduct outreach through community engagement, healthcare provider collaborations, and digital platforms to identify potential participants. Screen prospective patients by reviewing medical histories, verifying eligibility criteria, and explaining study procedures clearly and empathetically. Coordinate with clinical staff to schedule screenings, informed consent discussions, and follow-up appointments. Maintain accurate documentation of recruitment activities, patient interactions, and screening outcomes in electronic data management systems. Ensure all recruitment practices comply with FDA regulations, ICH GCP standards, HIPAA privacy rules, and clinical ethical guidelines. Monitor patient progress throughout the trial period, providing support and addressing any concerns related to participation or compliance. Skills Supervising experience in healthcare or research settings with the ability to lead recruitment teams effectively. Strong knowledge of medical terminology, clinical research methods, and healthcare compliance standards including FDA regulations and HIPAA. Proficiency in data management tools such as statistical software, EMR (Electronic Medical Records) systems, and Microsoft Office Suite. Experience reviewing clinical documentation for accuracy and completeness; familiarity with CDISC standards is a plus. Certification in ICH GCP (Good Clinical Practice) from a recognized issuer; valid CA certification preferred. Background in clinical laboratory procedures such as blood sampling, phlebotomy, vital signs measurement, and patient monitoring. Excellent analysis skills for assessing patient eligibility data; project management experience in healthcare or clinical trials is highly desirable. Knowledge of clinical quality assurance standards and compliance management practices within research environments. Ability to coordinate multiple tasks efficiently while adhering to strict timelines; strong communication skills for engaging diverse patient populations. This role offers an engaging environment where your expertise directly contributes to advancing medical science while supporting patient-centered care initiatives. Join us in shaping the future of healthcare through dedicated research efforts!

Pay:

$20.00 - $27.00 per hour

Benefits:

Flexible schedule Health insurance Paid time off Retirement plan

Work Location:

In person