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Kaiser Permanente Careers

Research & Development

Innovation in Practice

Operating one of the industry’s largest and most respected research programs, Kaiser Permanente employs nearly 1,800 research experts at 9 specialized centers across the country. With a research budget of $221 million and more than 2,500 studies and clinical trials underway at any given time, this is a place where you can have a profound impact on the future of health.

CT Regulatory Specialist II

Location: Oakland, CA Additional Locations:
Job Number: 776251 Date posted: 03/20/2019
Description:

The Clinical Trial Regulatory Specialist II (CTRS-II) is a position with demonstrated proficiency which, under the direction of the KPNC clinical trials administrative management or designee and Principal Investigator (PI), provides regulatory document support to the Kaiser Permanente Northern California (KPNC) PI and research site(s) conducting multiple FDA-regulated or other clinical trials. The CTRS-II has demonstrated proficiency in providing operational support for Sponsor and IRB regulatory compliance. The CTRS-II works independently and assumes increased responsibilities. This position is also responsible for assisting in protecting the health, safety, and welfare of research participants. This is a non-licensed position which must adhere to the position's scope of practice as outlined in the Major Responsibilities below.



Essential Functions:
- Compliance:  Support & comply w/ the Principles of Responsibility (Kaiser Permanente Code of Conduct).
- W/ guidance from PI & KPNC Clinical Trials Compliance Director, assist w/ ensuring compliance w/ Standard Operating Procedures (SOP) & document applications.
- Adhere to Guideline for Good Clinical Practice (GCP), federal, state, & local regulations, & KP policies & procedures.
- Assure all site documents including SOPs & administrative files are maintained in audit-ready condition.
- Assist w/ internal & external audits & quality assurance activities including monitoring visits, audits & inspections.
- Support the cost effective financial aspects of the clinical trial.
- Study Implementation: Prepare the following IRB documents; New protocol applications; KP consent form draft; Protocol modification forms; Adverse Event/Serious Adverse Event summary for annual report; & IND Safety Report Summary sheet for annual report.
- Assist the PI & other designated research staff in the preparation, submission, & maintenance of the following study-related regulatory documents: Current & obsolete versions of protocol & consent forms; FDA form 1572 and/or 1571; Protocol violations/deviations; Serious adverse events; Current & obsolete Investigation Drug Brochures; Documentation of IRB submissions & related correspondence, reports, & letters; Current laboratory certifications & normal reference ranges; Research staff CVs & licenses, training materials, & certifications; & Test article accountability forms, signature logs, etc.
- Perform duties such as filing, photocopying, faxing, & distributing study-related documents.
- W/ direction from PI, assist in preparation of annual, interim & final KPNC IRB reports.
- Maintain current licensure documentation including MD/RN licenses & CVs.
- Maintain training & education documentation for research personnel.
- Obtain regulatory certifications including KP laboratory state licenses, current laboratory certifications & normal reference ranges.
- W/ direction from PI, communicate & coordinate w/ the Sponsor regarding study document regulatory file activities & functions, including scheduling & conducting Sponsor-initiated monitor visits & following-up on outstanding items.
- Coordinate w/ the PI & internal/external parties regarding the collection & maintenance of regulatory IRB & other documentation & procedures.
- Perform data entry of study activities into a database program to track pertinent study activity (i.e. , study enrollment, consents, protocol violations/deviations, serious adverse event reports, & IRB history).
- Maintain all study-related legal & financial documents in separate confidential regulatory file in a timely manner, as requested.
- This job description is not all encompassing.

Basic Qualifications:
Experience
- Minimum three (3) years of project management experience in clinical trials research or human subjects protections required.
Education
Associate's degree.
Licenses, Certifications, Registrations
- N/A.

 

Additional Requirements:
- Proficient in electronic health systems and databases used in research environment, word-processing and spreadsheets.
- Proficient in medical terminology.
- Demonstrates written, verbal, and interpersonal communication skills.
- Attentive to detail and accuracy.
- Effectively manages multiple tasks with strict timelines.
- Demonstrates prioritization and organizational skills.
- Problem solving skills.
- Flexible and dependable.
- Works effectively on cross functional teams.
- Presents a professional manner and appearance.
- Comprehensive knowledge of the principles, methods and procedures of basic medical and/or clinical research processes.
- Comprehensive knowledge and understanding of human research protection regulations, policies, procedures, and standards as applied to IRB and compliance operations.
- Comprehensive knowledge of GCP, federal, state, and local regulations including HIPAA and KP policies and procedures.
- Must be able to work in a Labor/Management Partnership environment.

 

Preferred Qualifications:
- Minimum two (2) years of work experience in an ambulatory and/or acute health care setting preferred.
- Bachelor's degree preferred.
- CIP, CIM, ACRP, SOCRA or RAC certification preferred.
Primary Location: California,Oakland,2000 Broadway 2000 Broadway Scheduled Weekly Hours: 40 Shift: Day Workdays: Mon, Tue, Wed, Thu, Fri Working Hours Start: 9:00 AM Working Hours End: 5:30 PM Job Schedule: Full-time Job Type: Standard Employee Status: Regular Employee Group/Union Affiliation: Salaried, Non-Union, Exempt Job Level: Individual Contributor Job Category: Research and Development Department: Div of Research Travel: No Kaiser Permanente is an equal opportunity employer committed to a diverse and inclusive workforce. Applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), age, sexual orientation, national origin, marital status, parental status, ancestry, disability, gender identity, veteran status, genetic information, other distinguishing characteristics of diversity and inclusion, or any other protected status.

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 and state laws, as well as applicable local ordinances, including but not limited to the San Francisco and Los Angeles Fair Chance Ordinances.

About Research & Development Careers

Careers in Research & Development

Recognized worldwide for their scientific expertise, our researchers collect data on topics including cardiovascular disease, diabetes, mental health, and drug safety — just to name a few.

In addition to studies centered at these facilities, our physicians and researchers conduct clinical trials of new drugs, medical devices, and other therapies through several organized centers and independently at single sites. Put together, Kaiser Permanente's research centers and scientists comprise one of the largest and most comprehensive nonacademic research programs in the United States.

As a member of this team, you'll engage in meaningful work that has the power to affect outcomes and improve global health. Focused on areas like public-sector health services, epidemiology, and behavioral and clinical research, the work you do will ultimately allow us to improve the cost effectiveness and quality of the care we deliver — all while saving lives.

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