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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
Position Purpose:
Primary Duties:
Responsible for relationship building and management
Responsible for proactively providing local intelligence
Accountable for study start-up, activation, and execution to plan for targeted sites
For all sites
Responsible for CRO and Study Management interface
Responsible for process, standards, and oversight
Apply knowledge of data and analytics to target site and study, recommend and implement actions for mitigation and control
Protocol Site Oversight
Site and Study Management Interface
General
The Individual:
About the Job
About this Role
Manage Projects & Technology
Documentation
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.
Use the link(s) below to apply on company website.
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