Work Location: onsite in Glendale, CA

Please note this posting is for a future need

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. The Clinical Recruitment Coordinator 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 (including but not limited):

• 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. 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 record and progress note. 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:

• 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 Spanish and English - required

• A Bachelor’s degree; equivalent relevant work experience will also be considered.

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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.