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Parexel

End-to-end clinical trials and regulatory consulting

Clinical Research Nurse

Nursing & Frontline Patient CareConfirmed live in the last 24 hours
Full-timeGlendale, CA, USAIn-person

About the Job

Requirements

  • At least 2 years of experience working in a hospital or clinical setting.
  • A Bachelor of Science in Nursing is preferred, or relevant work experience.
  • An active Registered Nurse license in California is required.
  • Current Basic Life Support certification is required.
  • Advanced Cardiovascular Life Support certification is required within 6 months of the start date.

Responsibilities

  • Support Standard Operating Procedures, Good Clinical Practices, and work processes to ensure efficient and compliant clinical operations of the Early Phase Clinical Unit.
  • Assume responsibility for patient care and study conduct assignments.
  • Ensure study laboratory and medical tests are completed and study-specific eligibility requirements are met; assess compliance and symptoms according to the study protocol; and arrange pre- and post-procedure laboratory work.
  • Ensure established timelines for areas of responsibility and assigned projects are met.
  • Participate in and potentially direct identification and enrollment of study participants; contribute to developing and implementing study and research objectives.
  • Assess, monitor, record, and report patients’ conditions and reactions to drugs and treatments to the appropriate physician.
  • Collect and prepare data, and organize and enter data into case report forms.
  • Enter data into databases when required; assist physicians in completing flow sheets and progress notes in medical records; and update and maintain the Clinical Study File.
  • Perform or arrange phlebotomy, urine collection, sample preparation, storage and shipment, and drug dispensing; follow Good Clinical Practice quality documentation requirements.
  • Act as a participant advocate in clinical studies.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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