HOPA/ASCO QTP® 6-Month Thematic Program - Precision Oncology
HOPA is pleased to announce the next HOPA/ASCO QTP® 6-Month Thematic Program focused on Precision Oncology.
This program is the only oncology-focused quality improvement training for pharmacists, making it a unique opportunity for networking, knowledge sharing, and professional development. The program seeks to educate oncology pharmacists and their multi-disciplinary teams in designing, implementing, and leading successful quality improvement (QI) activities at their institutions.
Looking for 10 Pharmacist-Led, Multi-Disciplinary Teams from Community and Academic Settings to Participate!
HOPA will sponsor ten teams of 3-4 practitioners from institutions across the United States on their quality journey. Our goal is to have an even mix of teams from large academic medical centers and smaller community practice sites. All teams will be led by an oncology pharmacist and HOPA member, and will select a problem to address at their institution around the theme of Precision Oncology.
Applications are open now through Wednesday, Dec. 3 at 11:59 p.m. CT!
Over the course of the 6-Month Program, teams will attend one virtual onboarding session (one hour) and three in-person learning sessions (five days).
- Learning Session 0 - February 2026 (Exact date TBD), virtual
- Learning Session 1 - Saturday, March 28 and Sunday, March 29, 2026 in New Orleans, LA, in-person
- Immediately following the HOPA Annual Conference 2026
- Learning Session 2 - Thursday, June 11 and Friday, June 12, 2006 in Rosemont, IL near O'Hare Airport, in-person
- Learning Session 3 - September 14, 2026 in Washington D.C., in-person
- Offered as part of HOPA's 2026 Fall Programming Week
Criteria for Participation
All teams must meet the following criteria for participation:
- Assemble a core team of 3-4 participants, led by an oncology pharmacist (HOPA member in good standing)
- Core team members are required to attend the three in-person learning sessions
- Assemble a larger team that will support the institution at the practice level
- Designate a team sponsor (typically a senior institutional leader) to support their work
- Identify a quality problem for the improvement project
Program Fees & Policies
Payment & Reimbursement Policies
- Selected teams will be required to pay a program fee of $1,899 to HOPA in order to participate. This fee may be paid by the team's institution, or by the team members themselves.
- HOPA will cover flight and lodging costs for team members attending the in-person learning sessions. Meals (other than those provided during the in-person sessions), ground transportation, and other incidentals will not be eligible for reimbursement.
- Invoices will be sent when teams have been notified of their acceptance and confirmed their participation in the program. The program fee must be paid prior to the first learning session. Payments are non-refundable or transferable.
Reporting & Publication Policies
- HOPA has received funding from industry partners to help support this program. If accepted to this program, teams will be required to submit a midpoint report on the progress of their projects that will be shared with our partners.
- After the completion of their project, teams will be required to publish their findings in order to share what they have learned with a broader audience. This may include publication in abstract, poster, or manuscript form. Acceptable publication venues include HOPA Annual Conference, ASCO's Annual Meeting, the ASCO Quality Care Symposium, and/or in peer-reviewed oncology/pharmacy/healthcare quality journals.
- For the full list of 6-Month Program participation policies, click here.
To learn more about the Quality Training Program, please visit ASCO's website.
Click here to apply!
Please contact research@hoparx.org with any questions you may have as you are completing your application.
Need a Project Idea?
To help spark inspiration, the Precision Oncology Task Force has put together a list of example project ideas that may be submitted as part of your application. Your project does not have to align with one of these ideas, as long as it aligns with the overall theme of Precision Oncology.
Please reach out to research@hoparx.org if you would like feedback on your project idea!
Genomic Testing & Interpretation
- Improving turnaround time for biomarker testing or interpretation of results
- Standardization of tissue reflex to HER2 immunohistochemistry (IHC)
Patient Engagement & Equity
- Increase patient understanding of biomarker testing results
Data Integration & EHR Optimization
- Improving EHR integration of genomic tests to ensure genomic data is structured, searchable, and interoperable
- Enhancing compliance and patient trust in data handling practices
- Implementation of standardized reporting mechanisms for genetic testing results
Care Delivery & Clinical Pathways
- Academic-community pharmacist partnership for precision medicine integration
- Establishing collaborative practice agreements within oncology practice and local pathology departments for appropriate test selection to reduce QNS and improve time to test and time to treatment
- Establishing multi-disciplinary team to create workflow for ordering, interpreting, and providing recommendations for results (creating process in which testing happens for all appropriate patients with goal to test sooner and prevent treatment delay)
Curious about what a final QTP project may look like? Check out this project from the UConn team who participated in the 2023 HOPA/ASCO QTP 6-Month - Oral Chemotherapy Thematic: "Improved Oral Anticancer Medication (OAM) Adherence/Toxicity Assessment Documentation: A Quality Improvement Initiative"
Frequently Asked Questions
ASCO's Quality Training Program (QTP) is a well-established, data-driven course in quality improvement for oncology providers who need to measure performance, investigate quality and safety issues, and implement change. The course is led by a faculty and coaching team of quality improvement specialists with oncology experience.
Pharmacists are key members of the cancer team who often lead efforts to enhance quality of care for cancer patients. By participating in this program, team members will gain the tools and strategies necessary to drive change at their institution. This course is designed for interdisciplinary teams of 3-4 practitioners, with a HOPA member pharmacist serving as a Team Lead.
Oncology pharmacists are essential contributors to precision oncology programs at their institutions, offering critical expertise in selecting and optimizing biomarker-driven therapies to support the cancer care team. Their deep knowledge of pharmacogenomics, drug interactions, and personalized dosing helps ensure targeted treatments are used safely and effectively - ultimately enhancing patient outcomes and minimizing adverse effects.
Having teams work on projects that fall under the same theme helps to facilitate better collaboration and shared learnings. Throughout the program, teams can help each other by sharing tools, resources, and best practices, and work together to overcome barriers. By participating in this program, teams will gain insights into how institutions operationalize precision oncology work around the country, while improving the programs at their own institutions.
Material covered at the One-Day Workshops serve as a launching point for the more in-depth training in oncology quality improvement offered during this program. Teams are paired with quality improvement experts who will serve as their coach throughout the 6-month period and help them take their projects from inception to completion. Teams will also come together for 5 days of in-person learning over the course of three learning sessions.
*Previous participation in a HOPA/ASCO QTP One-Day Workshop is not required to participate in the 6-Month Program.
HOPA recognizes the interest of our members in expanding their knowledge of both precision oncology and oncology quality improvement. We also acknowledge that funding opportunities from individual sites may be limited, which is why HOPA, in collaboration with the sponsors of the Precision Oncology Initiative, is funding the majority of the cost of the programming.
Participants are expected to attend 6 full days of training over the 6-month period. The initial onboarding session will be offered virtually, with the remaining five days of training offered in-person across three learning sessions. The first session is two days at the beginning of the course (March 2026). The second session is two days at the mid-point (June 2026). The third and final session is one day at the end of the six months (September 2026).
Program participation will officially begin once teams have been notified and confirm their acceptance into the program. It is likely that teams will need to collect baseline data for their problem statement prior to the first in-person learning session in March 2026. Teams will convene virtually with their coach in between the in-person learning sessions to work on the next phases of their project. Program commitment will end when the team has completed their QI project and published their results (typically 6-12 months after the final in-person learning session in September 2026). Teams should expect to spend two or more hours each week on their project.
Team Leads are required to be oncology pharmacists and HOPA members with good standing in order to participate in this program. Leads should have the support of the leadership/administration at their institution to commit time to the identified project. In addition, Leads should be knowledgeable of the content matter for the project, have strong organizational and communication skills, and be adept at leading a team.
Teams should be made up of 3-4 staff from your institution (including the Team Lead), and interdisciplinary teams are encouraged. The makeup of your team will depend on the problem you are trying to solve and should include staff from any area affected by the QI project (clinical, operational, or administrative). This may include pharmacists, pharmacy technicians, physicians, nurses, APPs, practice administrators, data analysts and informaticists, and/or quality specialists.
Identification of a project sponsor is also important for your project to be successful. The sponsor typically does not attend the in-person courses but supports the team by removing obstacles and providing needed resources at the site. The sponsor is typically an administrative or pharmacist lead at the site.
All projects are required to fall into the theme of precision oncology. Please consider the following when selecting your project:
- Small, discrete tasks that need to be completed regardless may not be a good fit for a QI project
- Most people will perform a job well if they know how to perform the function and understand they are accountable and there are consequences for not completing the task
- Large, complex projects such as IT implementations and practice transformation are likely to require extensive planning and resources, and will take longer than 6 months to complete, so these are not good choices for the Quality Training Program
- Problems in practice where the cause is not known might be a good potential project for the Quality Training Program
- The QI projects completed during the QTP require an analysis of causes, collection of data, and a multidisciplinary team to improve the process
Not too large: Often a project team starts with a goal to improve a process for the entire practice and later reduces the scope to only a specific disease type or some subset of the full patient population. Starting small enables a project team to test and refine an idea before rolling it out to the entire practice. Later, the intervention can spread to the rest of the practice.
Not too small: Do not set the scope to a narrow population with a project to reduce or eliminate rare events. For example, if the scope of the intervention is limited to solid-tumor lung cancer patients for the project of reducing patients who die in the ICU, possibly not enough patients would be seen in a week or a month to fully assess the results of the intervention.
Just right: The Quality Training Program improvement phase is typically 10-14 weeks (between Session 2 and Session 3). Within that time, teams should plan and execute at least one, and possibly two or three tests of change, and each test of change should evaluate at least 20 patients. A test of change will take 2-4 weeks, so the scope should be broad enough to have about 20 patients during that period.
The Improvement Coach assigned to the project team can help determine the appropriate project scope.
No, ACPE or BCOP credits are not offered for this program.
Unfortunately, HOPA is not able to offer any positions to international teams at this time.