Training Opportunities for Clinical Research Personnel
The STUDY SET-UP stage includes activities that occur after the study has been designed and developed, and before you begin to enroll patients.
This stage includes activities in areas such as:
- contracts & grant proposals
- IRB approval
- research management compliance
- study budgeting & billing
- required registration of trial
Spectrum OTC provides education, required training and professional growth opportunities to the Stanford clinical research community.
Whether new to Stanford or in need of a refresher course, the below list of training programs provides the information necessary to successfully conduct clinical research at Stanford.
REQUIRED TRAINING FOR CLINICAL RESEARCH PERSONNEL
- Collaborative IRB Training Initiative (CITI)* (Required)
Required human subjects training for all staff who work on research projects (all investigators and other study personnel, including all persons who are responsible for the design, conduct, data analysis or reporting). More »
- Orientation to Clinical Research at Stanford (General Orientation)
Required for new employees who are working in clinical research. At this orientation Spectrum OTC staff will meet with clinical research personnel to provide resources and tools to successfully navigate research studies at Stanford. More »
- Health Screening, Safety and Compliance Training
Required for all non-faculty Stanford School of Medicine clinical research personnel (and postdocs) involved with human subject research. Supervisor to complete Clinical Researchers Occupational Exposures Assessment Questionnaire on new employee/postdoc's behalf.
- Budgeting and Billing Training
Required for all new and current employees who work on clinical research projects, if involved in budgeting and billing. Spectrum OTC offers monthly training sessions. More »
- Environmental Health and Safety Training Assessment
Everyone in the Stanford community is required to take some safety training. To clarify what safety training is necessary for each job function, Environmental Health and Safety developed the Training Assessment online tool for determining what safety training a SU employee needs to take. More »
- HIPAA Training
Stanford HIPAA training is required for every member of the workforce who comes into contact with Protected Health Information (PHI). More »
- eProtocol Training
eProtocol is an online application used at Stanford to submit, review, and approve research (human subjects; stem cells; animal subjects; and biosafety). More »
- GCP Training through CITI
If you are new to research or just need a refresher course, Good Clinical Practice (GCP) guidelines are available on-line through the IRB’s CITI training. More »
EDUCATION / WORKSHOPS
- Find a Workshop
View upcoming CTR educational workshops offered by Spectrum and affiliates, past presentations and videos, a list of courses, or request a workshop. More »
- Request a Workshop
View list of workshop topics, or suggest a topic. More »
OTHER TRAINING RESOURCES – STANFORD
- Lane Library
Lane Library’s instructional program supports clinical and bioresearch clientele with a class list that includes PowerPoint; Finding Funding; Basics of R Programming; Improving Your Scientific Writing Skills, and dozens more. More »
- Epic Training
Epic Training is required for all Stanford Hospital and Clinics physicians and medical personnel who need access to Hospital Medical Records.
Training is completed online. The specific courses that you are required to complete are dependent on your specialty, sub-specialty and scope of clinical practice. More »
- Cardinal Curriculum
Cardinal Curriculum is designed to develop Stanford's research administration workforce by providing tools for individuals to build competencies, increase efficiency, and improve compliance with Stanford and sponsor requirements. Training classes, which can lead to certification, are organized into two levels and are geared to individuals as they develop from novice to expert in research administration.
These classes will benefit research administrators and all administrative staff who support sponsored research.
- Cancer Clinical Trials Office (CCTO)
The CCTO provides training and quality assurance programs for both new and existing research staff to ensure that Cancer Institute research staff are current on all regulatory requirements as well as SCI standard operating procedures. More »
- Tech Training
Stanford University Information Technology Services (ITS) provides technology courses. See the ITS website for training options in the classroom, online, one-on-one by appointment, and custom classes. More »
The Stanford Training And Registration System (STARS) is Stanford's Learning Management System. Log in to Axess to see the STARS Training website which includes a “STARS Browse Catalog” and a “Training Needs Assessment” tool. More »
- Learning and Organizational Effectiveness
LOE Calendar of Course, Programs, and Conferences. More »
- Office of Sponsored Research (OSR)
The OSR website provides a list of recommended classes for those working with sponsored research. More »
PROFESSIONAL DEVELOPMENT RESOURCES – NON-STANFORD
ACRP is the primary resource for clinical research professionals in the pharmaceutical, biotechnology and medical device industries, and those in hospital, academic medical centers and physician office settings. More »
- University of California Santa Cruz, Extension
The UCSC Extension Certificate in Clinical Trials Design and Management is designed to help professionals gain a solid understanding of the entire clinical trials process, as well as a foundation in the scientific principles, regulations, and ethics that are vitally important to the conduct of clinical research. More »
- San Francisco State University Extension
Through the Clinical Trial Design and Management Certificate Program students may complete a full certificate or simply take those courses which advance their own professional goals. The program is designed to be flexible for working adults by offering evening or weekend courses. More »
- University of California Berkeley Extension
UC Berkeley Extension offers a Certificate Program in Clinical Research Conduct and Management which enables you to master practical aspects of clinical trial conduct and management, including clinical trial phases and design, planning, implementation, data analysis, regulatory and procedural guidelines, and ethical considerations. More »
- Some of this training is required before any research participants can be enrolled in a clinical study.
- You are responsible for maintaining training compliance for yourself, and if you are a PI, that of your research team.