Urgent requirement for one of our top clients located in “Irvine, CA”.
Please contact me at your earliest convenience, along with job No. CTM_112307 to xxxxxx.xxxxxx@xxxxxxxxx.xxx
Job Description:
Responsible for managing the clinical project team for one or more clinical protocols. Functions as an expert resource for clinical trial monitoring activities. Proposes staffing for new and/or existing projects. Responsible for managing clinical studies in accordance with Company’s SOPs, GCPs, FDA and ICH regulations.
Study termination including resolving data query forms, reviewing record retention requirements, and securing and reviewing an investigator’s report to the Ethics Committee or IRB as required. Participation in protocol development and CRF design. Monitors capacity of staff and assigns sites to maintain equity within the group taking into account CRA capabilities and level. Responsible for the following areas directly or indirectly through clinical research and associates:
· Site selection including completion of qualification visits
· Site initiation
· Completion and approval of monitoring reports within prescribed timelines
Requirements:
Bachelor’s degree in a biological science. Requires a minimum of 5 years experience working as a Clinical Research Associate or equivalent with at least 2 years in a lead CRA position overseeing the activities of clinical research staff.
Contact:
The most effective way of communication is via email please forward us your updated WORD FORMAT resume (Address, Contact number and email is must) to *** xxxxxx.xxxxxx@xxxxxxxxx.xxx ***
Please mention your best hourly rate, availability and visa status. Any questions, do feel free to email us.
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