Clinical Research Support

Training and Events

CRS TRAINING

2017

July 26, August 23rd & August 25th

CRC Summer Training Series


Registration for the CRS Clinical Research Coordinator Summer Series is now open! 

When? The training series will take place over 3 separate days in July and August. You are not required to sign-up for the entire series – you may select individual sessions.  

Who should attend?  These sessions are designed for both new and more experienced personnel within the Consortium – Clinical Research Coordinators, Data Coordinators, Regulatory Coordinators and Research Nurses.

How do I register?  Seats are limited so email Genevieve Meyer (gmeyer@fredhutch.org) as soon as possible.  If sessions are full by the time your registration form is received, your name will be added to a wait list.  We will then contact you if space becomes available.

Please contact Genevieve Meyer if you have any questions regarding this training. 

Dates

Times

Topic and description

Room Location

Wednesday,

July 26th  

10:00 a.m. – 12:30 p.m.

CAPA Workshop- This session includes interactive learning opportunities to help identify the root cause of an event, distinguish between corrective vs. preventive actions, and explore considerations for a successful CAPA implementation.

Facilitated by Genevieve Meyer, CRS Training Specialist, with co-presenters Jenn Davies and Nelson Spencer, CRS Regulatory Affairs Associates.  

Arnold

M1-A303

Wednesday,

August 23rd

10:00 a.m. –
10:30 a.m.

Data Abstraction Overview- This session provides an overview of the Data Abstraction Department and the various services they provide for transplant and non-transplant studies conducted within the Clinical Research Division (CRD).  Coordinators will learn about specific data capture requirements for Gateway and protocol registration, the role and responsibilities of the Consent Coordinator in the transplant consenting process, and the purpose and structure of the Optical Web Library (OWL).

Presentation by Linda Glockling, Fred Hutch Data Operations Manager

Arnold

M1-A303 & A305

11:00 a.m. –
12:00 pm

SCCA Research Charge Capture Invoicing Lifecycle- This session covers the SCCA Research Charge Capture/Invoicing Lifecycle in the context of clinical trials. Study staff will learn about specific processes and roles relating to charge capture and compliant billing practices. The goal of this session is to provide an overview of clinical trial billing from study startup and enrollment to final study close out.

Presentation by Azure Kraxberger SCCA Revenue Cycle Education Specialist and Kris Pedersen, SCCA Clinical Research Billing Analyst Lead

Friday,

August 25th

10:00 a.m. –
11:30 am

DOA Workshop- This session will look at common mistakes when completing the Delegation of Authority logs, review who should be listed and when, and learn ways to assure compliance.

Facilitated by Genevieve Meyer, CRS Training Specialist, with co-presenters Jenn Davies and Nelson Spencer, CRS Regulatory Affairs Associates.  

Arnold

M1-A303

 

 

CRS EVENTS

2017

July - Wednesday 12th

CONSORTIUM STUDY COORDINATOR MEETING


        Where:
                    Arnold, M1-A305/A307

        Time:
                    10:00am-11:00am

        Contact:
                    Clinical Research Support, 206-667-4520

        Topic: 
                    Reflections from an ACRP Conference

        Speakers:
                    Brandi Bratrude, Kelly Crowder, Sonia Goya, Susan Lemmon, Roxanne Moore, and                     Bethany Murphy


        Agenda:
                    10:00 - 10:05 - Welcome
                    10:05 - 11:00 - Presentations and Q&A

 

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