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Associate, Clinical Trial Management
Job Opportunity at
MEIRxRS / Med Exec Intl
Posted on Jul 30
Associate degree or higher preferred
1-2 year relevant experience in pharmaceutical industry or CRO
Experience supporting clinical trials preferred
Basic knowledge of drug development and FDA GCP/ICH regulatory guidelines is a plus
Experience using electronic data capture (EDC) systems is a plus
Financial management experience is a plus.
Support study feasibility activities and perform database/web searches for sites as needed
Work closely with the Site Start Up (SSU) and ensure all study related regulatory and financial documents are collected and reviewed in support of study activation
Organize and maintain project working files and track critical documents
Reconcile and transmit all essential documentation
Manage calendars and appointments. Resolve scheduling conflicts as needed.
Manage and coordinate travel requirements for group, consultants, and partners.
Prepare and oversee expense account reporting. May contribute to tracking budgets as needed.
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