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PAREXEL has proven to be a trusted partner for the complex development journey required of biopharmaceutical and medical device companies. We’re also an astute guide, able to simplify that journey for our clients, so safe new products can reach patients more quickly. - See more at: https://www.parexel.com/company#sthash.G0bQx8Mi.dpuf
About the Job
About this Role
General areas of responsibility also includes:
eCRF design, edit check programming, edit check validation and integration of third-party systems with the EDC databases.
All tasks should be performed in accordance to corporate quality standards, SOPs/Work Instructions/Guidelines, ICH-GCP and/or other international regulatory requirements.
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