Clinical Research Resources
ANNOUNCEMENTS: UPCOMING EVENTS AND RECENTLY POSTED MATERIALS
7/10/2025: Important Announcement about NCI Cancer Therapy Evaluation Program (CTEP) Online Resources:
The CTEP website formerly located at ctep.cancer.gov, has been retired. (The ctepcore.nci.nih.gov sites for AURORA, CTEP-AERS, RCR, and other applications are not changing.)
- Content previously found on CTEP webpages has been relocated to the new Division of Cancer Treatment and Diagnosis (DCTD) website: https://dctd.cancer.gov/research/ctep-trials.
- Frequently used resources are included on the one-page Quick-Access guide: https://dctd.cancer.gov/research/ctep-trials/ctep-website-updates-one-pager.pdf.
- Updated links for Adverse Event (AE) reporting, Common Terminology Criteria for Adverse Events (CTCAE), and resources for Pharmaceutical Management Branch (PMB) agent management, Clinical Trials Monitoring Branch (CTMB) quality assurance, and person registration are available in the NCI Memo: New Website Links for CTEP Clinical Trials Resources. (Login with credentials used to access secure NCI / CTSU IT systems).
- Associated updated to SWOG.org cross-links to above and other resources previously located on ctep.cancer.gov are ongoing. We appreciate your patience while we update these links (updates are anticipated for completion by end of July). After July 31, 2025, if you attempt to access a cross-link to CTEP resources that is not working. Please let us know via email to training@swog.org. (As always, we appreciate you reaching out!)
Overview. The Clinical Research Resources webpages are comprised of links to useful resources posted throughout the SWOG website and within the FDA, OHRP, OCR, NIH, NCI, and professional organizations that are pertinent to conduct of clinical trials within the NCTN.
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Public Access:
▪ Clinical Research and Human Subjects Research Protection Training
▪ Clinical Investigator Resources
▪ Resources for Oncology Research Professionals
▪ Regulatory and Ethical Research Conduct References
▪ Resources for Research Site Pharmacists
▪ Patient Advocacy Resources
▪ Continuing Education and Training Programs -
SWOG Workbenches:
▪ Protocol Workbench
▪ CRA Workbench (login with your CTEP credentials), including:
▪ SWOG CRA Manual for Oncology Research Professionals
▪ Tools
▪ Study Chair Workbench (login with your CTEP credentials)
▪ VA Workbench
▪ NCI Affiliates (login with your CTEP credentials) -
SWOG Membership Resources (login with your CTEP credentials):
▪ SWOG Protocol Development Resources
▪ Developing SWOG Protocol Tracking Reports
▪ Contracts and Budgets
▪ The Hope Foundation Funding Opportunities
▪ SWOG Committee Resources:
▪ Oncology Research Professionals Committee
▪ Digital Engagement Committee
▪ Recruitment and Retention
▪ Accrual Resources
▪ Patient Advocate Committee
▪ Pharmaceutical Sciences and Drug Information Subcommittee
▪ Training for SWOG Members -
SWOG Active / Closed Protocols:
▪ Frequently Asked Questions
▪ Trial and Group (Bi-Monthly) Updates
▪ SWOG Quality Assurance and Audits, including:
▪ SWOG Best Practices Document
▪ SWOG Trials Accrual Reports
▪ SWOG Publications
▪ SWOG Study-Specific Training -
SWOG Quality Assurance Program
▪ SWOG Quality Assurance Audit Guidelines
▪ Trial Master File for FDA Registration Studies
▪ Serious Adverse Events
▪ Safety Reports (login with your CTEP credentials)
Feedback?
The Clinical Research Resources webpages are continuously updated. We hope that you find this information helpful. Feedback or suggested resource additions are welcome. Please send any feedback to: training@swog.org. Please allow 3-5 business days for response.