Parexel
Overview
Clinical Enrollment Coordinator (Mandarin Fluent) at Parexel Early Phase Clinical Unit. Onsite in Glendale, CA. Parexel Early Phase Clinical Unit supports the development of innovative new medicines and “first in human” trials as the first step in testing these treatments in humans. As a Clinical Enrollment Coordinator you will be exposed to different parts of the early phase unit and work closely with research associates, call center agents, clinical research coordinators, and others to ensure the enrollment process of study participants is completed safely while following standards and protocols. Starting your journey with Parexel includes an extensive induction program and ongoing training while following your individual career path. Responsibilities
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 the 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 budgets. Participate in team project meetings and provide regular updates for assigned studies. Develop and present training material to department staff for assigned studies. Arrange for pre/post procedure lab work 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. Enter data into database when required. Ensure all paper source documents are completed as required by protocol. Assist physician with completing flow sheets in medical records and progress notes. Update and maintain contents of the Clinical Study File. Support Standard Operating Procedures (SOPs), Good Clinical Practices (GCP), and all work processes to ensure efficient and compliant clinical operation of the EPCU. Qualifications and Profile
Prior experience in clinical research enrollment and/or experience as a coordinator in either early-phase or late-phase clinical trials. Highly Preferred: Experience in immunology or autoimmune research. Bilingual proficiency in both spoken and written Mandarin and English - required. A Bachelor’s degree; equivalent relevant work experience will also be considered. Compensation and Benefits
Base Pay Range:
$25.00 to $34.00 per hour Actual salaries may vary within the range based on education, training, experience, professional achievement, and location. Additional compensation may include Parexel’s annual performance-based bonus plan, annual salary reviews, and other total rewards incentives where applicable. We offer market-leading benefits including paid time off, 401k match, life insurance, health insurance, and other benefits in accordance with applicable plans. Employment Details
Seniority level: Associate Employment type: Full-time Job function: Education and Training Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care Our talent acquisition team will provide additional details on bonus plans or incentive programs for eligible roles.
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Clinical Enrollment Coordinator (Mandarin Fluent) at Parexel Early Phase Clinical Unit. Onsite in Glendale, CA. Parexel Early Phase Clinical Unit supports the development of innovative new medicines and “first in human” trials as the first step in testing these treatments in humans. As a Clinical Enrollment Coordinator you will be exposed to different parts of the early phase unit and work closely with research associates, call center agents, clinical research coordinators, and others to ensure the enrollment process of study participants is completed safely while following standards and protocols. Starting your journey with Parexel includes an extensive induction program and ongoing training while following your individual career path. Responsibilities
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 the 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 budgets. Participate in team project meetings and provide regular updates for assigned studies. Develop and present training material to department staff for assigned studies. Arrange for pre/post procedure lab work 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. Enter data into database when required. Ensure all paper source documents are completed as required by protocol. Assist physician with completing flow sheets in medical records and progress notes. Update and maintain contents of the Clinical Study File. Support Standard Operating Procedures (SOPs), Good Clinical Practices (GCP), and all work processes to ensure efficient and compliant clinical operation of the EPCU. Qualifications and Profile
Prior experience in clinical research enrollment and/or experience as a coordinator in either early-phase or late-phase clinical trials. Highly Preferred: Experience in immunology or autoimmune research. Bilingual proficiency in both spoken and written Mandarin and English - required. A Bachelor’s degree; equivalent relevant work experience will also be considered. Compensation and Benefits
Base Pay Range:
$25.00 to $34.00 per hour Actual salaries may vary within the range based on education, training, experience, professional achievement, and location. Additional compensation may include Parexel’s annual performance-based bonus plan, annual salary reviews, and other total rewards incentives where applicable. We offer market-leading benefits including paid time off, 401k match, life insurance, health insurance, and other benefits in accordance with applicable plans. Employment Details
Seniority level: Associate Employment type: Full-time Job function: Education and Training Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care Our talent acquisition team will provide additional details on bonus plans or incentive programs for eligible roles.
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