Patient Recruitment Coordinator - Baltimore, United States - Parexel

Parexel

Verified Company

Baltimore, United States

3 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

Baltimore, Maryland, United States of America

Job ID R

Category Clinical Trials

ABOUT THIS ROLE:

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.

At Parexel's Glendale, CA unit our highly trained and skilled Patient Recruitment Coordinator are crucial to ensuring the successful completion of Phase I trials. This role coordinates and assumes responsibility for study participant enrollment, care, and study assignment.

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:

Bachelor degree required or 3+ years relevant work experience
Highly Preferred: Fluent in English and Spanish (written and verbal) OR English and Japanese (written and oral)
At least 1year related experience working in clinical research preferably focused on patient recruitment/enrollment
Computer skills and familiarity with research process is required

EEO Disclaimer
Parexel is an equal opportunity employer.

Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.