Clinical Research Coordinator-SOM: Office of Clinical Research Department- Sacramento Campus
Our physicians conduct clinical research and collaborate closely with laboratory scientists, ensuring that new drugs, advanced biotechnologies and other treatments developed in the lab can move quickly to the clinic to benefit patients.
Job Summary Final Filing Date : 2/12/21 Salary Range : $28.17 to $45.29 Salary Frequency : Hourly Appointment Type : Career Percentage of Time : 100% Shift Hour : Varied Location : Office of Clinical Research City : Sacramento Union Representation : Yes Benefits Eligible : Yes
We offer exceptional employment benefits including medical, dental, and vision plans, generous paid vacations and holidays, excellent retirement savings and investment plans, continuing education, and reduced fee and scholarship programs.
THIS IS NOT AN H1- B OPPORTUNITY
Qualified candidates will be considered for interviews after 1/22/21.
Responsibilities The Clinical Research Coordinator is a health professional having working knowledge of clinical research activities, communication skills and a willingness to cooperate as a team member. Required is the use of skills to independently or with general direction coordinate and follow through in the overall administration and outcome of clinical studies.
Knowledge and experience with disease processes as applied to human clinical research.
Knowledge and experience with clinical research trials regulations (e.g., Food and Drug Administration [FDA] and Office for Human Research Protections [OHRP]).
Knowledge of and experience with regulatory processes as well as a working knowledge of data management activities as applied to clinical trial coordination.
Knowledge of and experience with basic anatomy, medical terminology and ability to interpret physicians' notes, medical records, laboratory and scan results.
Experience with Microsoft Office Suite: Word, Excel, Outlook, Access, etc.
Experience with tracking and recordkeeping.
Must have analytical skills to evaluate information, changes in practices and procedures, formulate logical and objective conclusions
Must have demonstrated oral communication and interpersonal skills to correspond effectively with the public, co-workers, physicians, patients, caregivers, clinic staff and other health care professionals.
Must display organizational skills and attention to detail so that large volumes of records can be accurately maintained to accomplish a task or goal in a timely manner.
Must display writing skills including ability to compose reports and correspondence while utilizing correct grammar, spelling and punctuation as well as clearly documenting research data onto forms.
Must be able to work independently and/or cooperatively as a team member in a diverse workforce.
Must be able to work occasional overtime as work demands.
Must be able to travel on occasion.
Previous experience coordinating clinical trials.
Position requires working closely with caregivers and with patients who have a terminal illness.
This position may be subject to a criminal background investigation, drug screen, Live Scan fingerprinting, medical evaluation clearance, and functional capacity assessment.
EEO The University of California is an Equal Opportunity/Affirmative Action Employer advancing inclusive excellence. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the UC nondiscrimination policy.
The University of California is an Equal Opportunity/Affirmative Action Employer advancing inclusive excellence. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the UC nondiscrimination policy.
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