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Clinical Enrollment Coordinator

Parexel


Job Location:

Glendale, WI - USA

Hourly Salary: $ 25 - 34
Posted: 31 May 2026 (30+ days ago)
Application Deadline: 28 August 2026
Vacancies: 1 Vacancy

Job Summary

When our values align theres no limit to what we can achieve.

At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.

Join Parexels 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) were dedicated to delivering life-changing medicines to patients worldwide.

Job Title: Clinical Enrollment Coordinator

Work Location: onsite in Glendale CA

Parexel Early Phase Clinical Unitsupports 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 anextensive induction program and ongoing training while following your individual career path.

What youll 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 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
  • Bachelors 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 Parexels 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.


Required Experience:

IC


About Company

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Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our the ... View more

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