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Job Field: Government Jobs
Location: Central Valley, CA
Salary: $Not stated

JOB SUMMARY:

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<tr><td valign="top" width="450"><b>Title: Clinical Research Coordinator-600 Coffee Road-Temp*Location: California-Central Valley-ModestoOther Locations:Clinical Research Coordinators are responsible for evaluating the appropriateness of potential new trials for SGMF working with interested providers. The Clinical Research Coordinator facilitates the legal review for trial specific contracts and negotiates the contractual budget for each new trial. The coordinator also ensures that all regulatory documents are filed for each trial, and supports the providers with fulfilling the necessary training and documentation requirements for each trial. Each coordinator is responsible for consenting patients into their trials and conducting patient visits per the trial protocol. The coordinator is responsible for all documentation related to their trial portfolio and managing the financial aspects for their trials (sponsor invoicing, payments to patients and providers)Sutter Gould Medical Foundation (SGMF)is a non-profit, multi-specialty health care organization affiliated with Sutter Health. Based in Modesto, SGMF provides quality medical care, health education and research activities in a five-county area. SGMF''s medical staff includes family practitioners, internists and pediatricians, as well as a range of specialist physicians. Services include imaging, nuclear medicine, a health library, health education programs, occupational medicine, diabetes education, nutrition counseling, infertility counseling, and weight management.Bachelor''s degree or equivalent combination of education and experience (8 yrs.). Preferred field of study is biology, nursing, or other science related field. Must be eligible and attain the status of Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC) through the Society of Clinical Research Associates or Association of Clinical Research Professionals within six (6) months of completing the two (2) year requirement of documented Research experience at own expense. Once certified, must be willing to maintain certification by taking required educational classes at own expense. Minimum of two years experience in working with patients either through direct patient care or in conduct of clinical research required. Previous experience in clinical research strongly preferred. Previous experience with personal computer applications, including Word and Excel required. Data management, email and electronic medical record experience preferred. The ability to lead work independently and manage time and workflow to meet deadlines is required. Excellent oral and written communication skills are essential. Strong critical thinking and problem solving are required. Must be willing to work with blood and tissue samples and operate certain research devices such as HemoCue, ECG machines, and Sponsor provided laptop computers for data entry. Knowledge of medical terminology strongly preferred. Basic anatomy, physiology, pharmacology and lab procedures enabling assessment of patient eligibility strongly preferred. Knowledge of clinical research trial principles including appreciation for protocol adherence and human subject research ethics strongly preferred. The ability to prioritize and manage multiple tasks facilitating maximum efficiency of workload. Excellent communication skills required to work effectively with internal and external customers. Basic computer skills to include Microsoft Word and Excel. Willing and able to learn individualized computer programs used by Sponsors for protocol required data capture. Must have strong attention to detail. Ability to work independently and manage time and workflow to meet deadlines. Travel to care centers and some over night travel may be required. Travel to annual conference for 4-5 days may be required. Over night travel to Investigator''s Meetings for trials may be required. Ability to participate in community events as representative of SGMF Clinical Research Departm

KEY REQUIREMENTS:

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