PRIM&R accepts advertisements from all institutions seeking to hire for positions in animal and human research ethics and related fields, such as research administration and ethics education; listing does not imply endorsement of the lister or of the qualifications stated for a position.
Promoting honesty and integrity across our daily actions and interactions, our compliance, privacy, and regulatory professionals provide the guidance and resources to uphold the highest ethical standards.
In this role, you will manage regulatory aspects of small to large scale research projects. You will work independently in accordance with established objectives. You will be responsible for performing regulatory review and analysis of research study submissions to the Kaiser Permanente Northern California Institutional Review Board (KPNCAL IRB) for consistency, completeness, and compliance with federal and state regulations and the Kaiser Permanente Northern California Institutional Review Board policies and procedures.
At least two years of experience in clinical research or clinical trials, clinical research compliance, and the protection of human subjects, or equivalent
A bachelor’s degree or four years of experience in a directly related field with a high school diploma or GED
The ability to learn and master proprietary software such as IRIS or IRBNET as these programs are critical to day-to-day operations
Experience with Microsoft Office Professional software
The ability to independently manage several projects at once and the ability to work under pressure
The ability to complete a medical terminology course within six months
Excellent interpersonal, oral, and written communication skills to work effectively with researchers, IRB staff, IRB members, senior leadership, and other customers
The ability to successfully and professionally communicate complex information to a wide variety of audiences
The ability to work in a Labor/Management Partnership environment
Preferred Qualifications Include:
A certified IRB Professional (CIP) or Certified IRB Manager (CIM) designation preferred or will be required to complete CIP/CIM certification when eligible
IRB coordinator and/or human research regulatory coordinator experience preferred
Working knowledge of scientific and medical concepts and terminology preferred
Experience reviewing Exempt and/or Expedited research
Experience working in an IRB or regulatory department and providing either regulatory or administrative support to an IRB Committee
For immediate consideration, please visit http://kp.org/careers for complete qualifications and job submission details, referencing job number 728089.
External hires must pass a background check/drug screen. Qualified applicants with arrest and/or conviction records will be considered for employment in a manner consistent with Federal, state and local laws, including but not limited to the San Francisco Fair Chance Ordinance. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, protected veteran, or disability status.
This position supports Kaiser Permanente’s code of conduct and compliance by adhering to all laws and regulations, accreditation and licensure requirements, and internal policies and procedures.
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Internal Number: 728089
About Kaiser Permanente
As America's largest nonprofit health plan, serving over 9 million members in eight states and the District of Columbia, we're driven by the needs of our patients and our responsibility to the communities we serve. We recruit high-caliber individuals and provide them with a positive work environment, outstanding facilities and resources, competitive wages, and exceptional benefits. If you believe quality of care and quality of life go hand in hand, this is the place to put your beliefs into practice.