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Clinical Research Associate I - II

Remote · North Ryde, New South Wales, Australia

Type
Full Time
Level
Mid Level
Education
Bachelors Degree
Company size
Large

Job Summary

Clinical Research Associate I-II at Parexel focused on site management and monitoring across Australian/NZ trials. Responsibilities include acting as primary contact for assigned sites, ensuring protocol adherence, addressing site issues, managing regulatory documents and site training, evaluating data quality and site performance, conducting on-site and remote visits, ensuring ICH-GCP compliance, and coordinating with CTMS/EDMS/TMF systems. Requires strong problem solving, ability to work independently, excellent communication, and willingness to travel. Education/experience: degree-level qualification in biological sciences, pharmacy, nursing or equivalent; site-management experience in clinical research; 1+ year of independent monitoring experience preferred. Travel and cross-cultural collaboration are expected; proficient in CTMS/EDMS and MS Office; capability to operate in a matrix environment.

Required Qualifications

  • Degree in biological sciences, pharmacy, nursing or equivalent
  • Site management experience in clinical research
  • At least 1 year of independent monitoring experience (AUS/NZ)
  • Educated to degree level with relevant health discipline preferred
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Parexel

Clinical Research Associate I - II

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