Clinical Enrollment Coordinator
$25 - $34 per hourParexel International
Join Parexel's team of changemakers as we help advance healthcare throughout the globe, all while keeping the patient at the heart of everything we do. As a leading Clinical Research Organization (CRO), we're dedicated to delivering life-changing medicines to patients worldwide. Job Title: Clinical Enrollment Coordinator Work Location: onsite in Glendale, CA Parexel Early Phase Clinical Unit supports the development of innovative new medicines which are vital for public health, improving outcomes, and saving lives. The early phase and “first in human” trials are the first step in testing these novel treatments in humans. As a Clinical Enrollment Coordinator you will constantly learn and be exposed to different parts of the early phase unit. This position works closely with research associates, call center agents, clinical research coordinators, etc. to ensure the enrollment process of study participants is completed safely while following standards and protocols. Starting your journey with Parexel comes along with an extensive induction program and ongoing training while following your individual career path. What you’ll do after training is completed Screen potential clinical trial volunteers according to protocol specific requirements and CFR/ICH GCP guidelines. Ensure all study laboratory and medical tests are completed and the eligibility requirements specific to assigned studies are met. Ensure all established timelines relating to area of responsibility and assigned projects are met. Ensure completion of enrollment for assigned studies and manage process closely to minimize waste. Ensure quality control (QC) performance of all electronic and paper source documents. Assist in reviewing Informed Consent Documents, Study Protocols, Source Documents, and Case Report Forms during development. Ensure screening ratio and marketing expenditures are maintained within study specific budget. Participate in team project meetings and ensure regular updates for assigned studies. Develop and present training material to department staff for assigned studies. Arrange for pre/post procedure lab work to be performed and initiate follow up as required. Ensure follow up to all queries related to screening and enrollment of assigned studies. Collect, organize, and prepare data for physician review and assist physicians with completing flow sheets in medical record and progress notes. Enter data into database when required. Ensure all paper source documents are completed as required by protocol. Update and maintain contents of the Clinical Study File. Support Standard Operating Procedures (SOPs), Good Clinical Practices (GCP), and all work processes to ensure the efficient and compliant clinical operation of the EPCU. Your Profile 2 years’ experience in clinical research enrollment and/or experience as a coordinator in either early-phase or late-phase clinical trials. Bachelor’s degree; equivalent relevant work experience will also be considered. Fluent in written and spoken English required; Spanish fluency strongly preferred . Experience in autoimmune research preferred but not required. Base Pay Range: $25.00 to $34.00 per hour Actual salaries may vary within the range based on several factors including, but not limited to education, training, experience, professional achievement, and location. In addition to base salary, some roles may be eligible for participation in Parexel’s annual performance-based bonus plan, annual salary review and additional total rewards incentives. Our talent acquisition team will provide additional details on our bonus plan or incentive programs for those eligible roles. For all eligible employees, we offer market leading benefit programs including paid time off, 401k match, life insurance, health insurance, and other benefit offerings in accordance with the terms of applicable plans. EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. #J-18808-Ljbffr Parexel International
- Parexel International is looking for a Clinical Enrollment Coordinator in Glendale, CA. This role involves screening clinical trial volunteers and ensuring compliance with protocols and timelines. The ideal candidate has 2 years of experience in clinical research enrollment...Suggested
$25 - $34 per hour
Join Parexel International in Glendale, AZ as a Clinical Enrollment Coordinator where you will coordinate the enrollment of participants in clinical trials. This role requires bilingual proficiency in Mandarin and English, with at least 2 years of experience in clinical...SuggestedHourly pay- Parexel International is looking for a Clinical Enrollment Coordinator to join our team in Glendale, CA. In this role, you will screen clinical trial volunteers, ensure enrollment processes follow established protocols, and maintain documentation quality. We value a collaborative...Suggested
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...subordinates for efficient time management. May be assigned to coordinate continuing education activities, lectures, presentations and... ...California license, preferably certified by ASCP (American Society of Clinical Pathologists) and additional certification in the area...Hourly payFull timeWork experience placementInternshipLocal area$26.77 - $34.32 per hour
University of Southern California is seeking a Clinical Data Manager to manage clinical data from medical records. The role includes data entry, maintaining regulations, and ensuring data accuracy in forms submitted for studies. Preferred candidates will hold an Associate...Hourly pay
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