2018-06-12

Clinical Trial Associate/Assistant
Job Opportunity at MEIRxRS / Med Exec Intl

Posted on Jun 12

https://meirxrs.com    818-247-1368

Location: Irvine, CA
Job Type: Contract
Job ID: W4161540

Our client needs a Contractor to work as Clinical Trial Associate. Contract is estimated for 12 months at their facility in Irvine, CA. Possibility for conversion to full-time after a year. We offer benefits including employer contribution to healthcare for this position. You must have authorization to work in the United States (sponsorship is not available).
  
Requirements. Must Have!
Associate degree or higher
1-2 year relevant experience in pharmaceutical industry or CRO
Experience supporting clinical trials preferred
Live within commuting distance of Irvine, CA


Expectation is 8 hour day, 5 days a week. Benefits include employer contribution to healthcare, 401k, and sick leave.

Primary Job Responsibilities
  • Perform tasks as assigned by their manager which includes but is not limited to preparing, collecting, and tracking master study level documents and site non-regulatory documents, reviewing, updating, and testing clinical systems, producing reports on clinical status, trends, and metrics, facilitating communication across all departments, supporting the monitoring team and study sites with relevant study information, and supporting clinical operations.
  • Ensure the assigned clinical study is run to time and budget and is completed in compliance with all relevant laws, regulations, and regulatory guidelines as well as all corporate policies and procedures.
  • Participate as a Global Clinical Trial Representative in cross-functional teams such as the Clinical Trial Team.
  • Support the study team by performing any of the following operational activities: study/site supplies, vendor activities, site newsletters, financial tracking, enrollment tracking, CT.GOV posting, trial master file management, attending internal meetings and vendor meetings as appropriate, taking minutes and supporting the study team in ad hoc activities.
  • Complete assigned tasks within agreed upon project priorities, timelines and quality specifications.
  • Other activities, special projects and assignments may be given as required
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