Senior Regulatory Clinical Research Coordinator- SOM: Office of Clinical Research Department- Sacramento Campus
The Office of Clinical Research is dedicated to conducting clinical trials that promote and support multidisciplinary collaborations. These will assist in the translation of our scientific discoveries to the clinic and ultimately bring more lifesaving treatments to our patients. Our mission is to offer our patients the most advanced, personalized therapies that will lead to a reduction in the morbidity and mortality from cancer.
Job Summary Final Filing Date : 1/29/21 Salary Range : $34.18 to $54.97 Salary Frequency : Hourly Appointment Type : Career Percentage of Time : 100% Shift Hour : Varied Location : Office of Clinical Research, FSSB, Suite 2200 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
Responsibilities The Senior Regulatory Clinical Research Coordinator provides leadership for a department-wide clinical research program, including mentoring and overseeing junior regulatory coordinators and/or other support personnel and possess advanced knowledge of regulatory processes as well as a working knowledge of data management activities. Additionally, the Senior Regulatory Clinical Research Coordinator requires certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals and is required to have advanced-level knowledge of federal, local, and institutional regulatory guidelines.
Certification by the Society of Clinical Research Associates (SoCRA) or the Association of Clinical Research Professionals (ACRP).
Experience with disease processes as applied to human clinical research.
Minimum 3 years of clinical trial coordination experience.
Advanced experience with federal, local, and institutional regulations and policies (e.g., Food and Drug Administration [FDA], Office for Human Research Protections [OHRP], and Good Clinical Practice [GCP]).
Advanced experience with IRB policies and procedures.
Advanced experience with anatomy and medical terminology.
Experience with training and coaching others.
Experience with Microsoft Office Suite: Word, Excel, Outlook and Access.
Experience with databases and/or Clinical Trial Management System and (CTMS).
Experience maintaining large volumes of records.
Experience composing reports and correspondence while utilizing correct grammar, spelling and punctuation as well as clearly documenting research data onto forms.
Experience coordinating oncology clinical trials
Must be able to work occasional overtime as work demands.
Must be able to travel on occasion.?
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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