The following message is official and has been approved by the appropriate authorities to be posted to this list. ++++++++++++++++++++ Institution: University of California San Francisco Position: Clinical Research Study Coordinator (full-time) Start date: As soon as possible
Job Description: Manage various aspects of clinical research trials conducted by principal investigator(s). Duties include but not limited to: 1) Coordinate the development of forms and applications to research committees and for regulatory purposes. 2) Recruit, screen and discuss the purpose of the study to participants; obtain informed consent; schedule patient for study procedure; initiate drug orders, laboratory procedures, and treatments for patients. 3) Collect data from patients from medical charts, interviews, questionnaires, diagnostic test and other sources; obtain blood samples, cultures and other specimens for laboratory analysis; perform 12 lead ECGs 4) Ensure compliance with protocol guidelines for sponsors and regulatory agencies. 5) Perform administrative duties to maintain the proper operations of the research studies. Please forward all resumes and questions to the following: Diana: [EMAIL PROTECTED] Thank you very much. Regards, Diana ---------------------------------------------------------------- The above message does not necessarily represent the views or opinions of MCBcDNA, mcbUSA, the MCB Department, or UC Berkeley. TO UNSUBSCRIBE FROM THIS LIST, send an email to [EMAIL PROTECTED] with "unsubscribe mcb-infoline" in the message body. Please send questions or comments to [EMAIL PROTECTED] For a list of upcoming events and information about the student clubs: MCBcDNA http://mcb.berkeley.edu/groups/mcbcdna/ mcbUSA http://mcb.berkeley.edu/groups/mcbusa/
