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Study Coordinator
Location:
Torrance, CA
Description:
Study Coordinator Required Skills & Qualifications : GED or high school diploma. Bachelor's degree desired. Nursing majors preferred. English proficiency. Bilingual English/Spanish desired. Proficiency with Microsoft Office (Word, Excel, Power Point, Outlook). Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) desired. Medical Assistant / LVN / RN or equivalent training. Ability to Draw Blood - Understand Medical and Research Terminology, Ability to perform 12 lead EKGs, Ability to Perform Spirometry, Ability to Draw and spin down blood, and ship or freeze samples, familiarity with -20 and -80 Freezers, Ability to enter data into CRFs, track and document contacts in a contact monitoring software program and interact with Study Monitors. 3 years as a study coordinator in a research or clinical trials environment. Organizational Communication (Phone, email, verbal, written) Computer Skills (Word, Email, Excel) Obtain Accurate Vital Signs Blood Drawing Spin down Blood in a centrifuge and package it for shipping or freezing (-20 and -80 Freezers) EKG Spirometry Ability to work as a member of a team and organize and distribute tasks collectively each day. Ability to work well under pressure and meet multiple and sometimes conflicting deadlines. Ability to interact in an appropriate and professional manner. Demonstrated cooperative behavior and very positive problem solving and conflict resolution skills. Available to work dependably and be flexible with scheduling, depending on workload. Description of Duties : Organizing Study related tests in house and outside. Communication with study subjects, perform complete research visits, interact with other coordinators, laboratory personnel, and family members. Data Entry Attend Regular Research and Laboratory Meetings, internal and external. Recruitment and retention of subjects into existing clinical studies Recruit/enroll patients into clinical trials. Maintain study documentation current, accurate, legible, and confidential (written and electronic CRF). Perform all study required visits, documentation, coordination, and subject related issues. Assist IRB duties and queries related to the initiation, continuance, and closure of studies. Stay current with all Lundquist required Human Resource training. Obtain informed consent. Obtain complete patient questionnaires. Work closely with other Study Coordinators & Principal Investigators on each day's task collectively. Maintain the subject schedule and remind subjects of upcoming visits. Travel to investigator meetings as required. Meet with study monitors from outside funding agencies. Work with other employees of Lundquist to establish a safe and efficient workplace environment. Interface with the research pharmacy personnel as needed. Update and keep current all IRB documents pertaining to current and past studies. Blood Drawing and Spin down and Shipping. Other duties as may be assigned. Salary Range: $28-38/hr. *MON PDN-9b72628e-78cb-45a7-8e3a-ce4985995484
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Study Coordinator is a Other Jobs Study Coordinator Job at Monster located in Torrance CA. Find other listings like Study Coordinator by searching Oodle for Other Jobs Study Coordinator Jobs.
Study Coordinator is a Other Jobs Study Coordinator Job at Monster located in Torrance CA. Find other listings like Study Coordinator by searching Oodle for Other Jobs Study Coordinator Jobs.