Site Feasibility
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Program Agenda:
Webinar replay #1: Attaining the Perfect Balance: Objective Protocol Feasibility Scoring
Speakers:
Christina Talley via pre-recorded webinar
Program Description: Increasing clinical trial complexity with leaner budgets demand the clinical trial site be more agile than ever. Sites must balance needs to effectively staff trials and distribute workload between team members or justify increasing staff to support growing demands. In order to do this, it’s critical to have methods to evaluate, quantify, and document how much effort will be required to execute a project. Protocol scoring or feasibility tools allow objective assessment toward operationalizing a trial and will aid in enhanced justification for protocol acceptance, workload leveling to increase investigation quality and overall participant subject safety.
Upon completion of this Seminar, attendees should be able to:
- Examine and understand the rationale for detailed protocol analysis to determine decision points for protocol acceptance and more effective workload distribution.
- Evaluate how feasibility and proactive planning can assist in overall work performance, raising workload quality, enhancing subject safety, and responsible financial management
- Discuss some of the current feasibility, scoring, and clinical trial tracking tools and their utilities
Webinar replay #2: Feasibility Questionnaire Completion: Effective Strategies for Site Success in a Highly Competitive Industry
Speakers:
Mallory Thomas via pre-recorded webinar
Program Description:
Completing a feasibility questionnaire is something that any successful research site is doing on a consistent basis. The question remains: how does a research site put their best foot forward in an increasingly competitive environment? This webinar will break down the basic and not-so-basic tactics that any motivated site should be practicing in completing feasibilities. Understanding what a sponsor is looking for in an ideal site, leveraging your site’s overall experience and past study metrics, and even when to accept or decline a study and why doing so would be beneficial to your site in the long run are all topics that will be discussed in this webinar.
Upon completion of this Seminar, attendees should be able to:
- Understand what sponsors are looking for in a feasibility questionnaire
- Identify strategies to increase a site’s chances of getting awarded a study
- Know when and how to convey information to a sponsor that may not be explicitly asked on a feasibility questionnaire
Target Audience:
- CRCs
- Investigators
- Clinical Research Administrators
Registration Cost: Free to all attendees
Contact hours: 2.0 Contact hours have been applied for through ACRP. Membership is not required for online registration of contact hours.
Contact Hour Cost:
- $0 Chapter Members
- $35 ACRP Members
- $50 Non-Members
To receive contact hours:
Purchase the contact hours, attend the program. Log on to the ACRP website then “ACRP Learning Portal” to complete the evaluation no later than 30 days following the event and obtain the online certificate.
Refund Policy: Contact melanie.hogg@atriumhealth.org to request a refund.
Level: N/A