Bilingual Enrollment Coordinator (English and Korean Fluent)
Parexel
Summary
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.
Job description
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 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
- Fluency in English and Korean, both written and verbal
Requirements
- 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
- Fluency in English and Korean, both written and verbal
Benefits
- Paid time off
- 401k match
- Life insurance
- Health insurance
- Performance-based bonus plan
Company overview
Parexel is one of the world's largest and most prominent contract research organizations (CROs), providing comprehensive clinical research services to pharmaceutical and biotechnology companies globally. Founded in 1982 and headquartered in Raleigh, North Carolina, Parexel operates with a global workforce of over 24,000 professionals across 84+ facilities in 49 countries. The company specializes in managing the full spectrum of clinical trials from Phase I to IV across diverse therapeutic areas including neuroscience, oncology, infectious diseases, hematology, and general medicine. Parexel offers end-to-end solutions encompassing clinical trial management, regulatory strategy, data management, biostatistics, pharmacovigilance, medical communications, and market access consulting. With a strong track record spanning over 40 years, Parexel has established itself as a trusted partner for both established pharmaceutical leaders and emerging biotech innovators, helping accelerate drug development and bring life-saving treatments to patients faster through its patient-centric approach and operational excellence.