Clinical Research Support

News and Events

CRS NEWSLETTERS

Find previous editions of the Clinical Research Support Newsletter below:

CRS CALENDAR OF EVENTS

April 2015

Friday, April 3

REGULATORY AFFAIRS OFFICE HOURS


        Where:
                Fairview Bldg, LF-223

        Time:
                9:30 a.m. - 10:30 a.m.

        Contact:
                Regulatory Affairs, 206-667-1394/206-667-7167

        Agenda:
                Regulatory Affairs availability for drop-in consultations. (Click here for more information.)
 

Monday, April 6

CLINICAL RESEARCH COORDINATORS TRAINING - DAY 1


What:

These sessions are designed primarily for those in a new role in clinical research, but some of these topics can also serve as refreshers for more experienced personnel within the Consortium – Clinical Research Coordinators, Data Coordinators, Regulatory Coordinators and Research Nurses.

More information -- including full agenda and registration form -- can be found here.

When:

The training series will be divided over three days in April 2015.

  • Day 1: April 6, 2015 (from 9:30 a.m. - 3:00 p.m.)
  • Day 2: April 13, 2015 (from 9:30 a.m. - 3:10 p.m.)
  • Day 3: April 20, 2015 (from 9:30 a.m. - 2:00 p.m.)


Contact:

Kersten Brinkworth, CRS Training Manager

Tuesday, April 7

CONSORTIUM STUDY COORDINATORS (CSC) MEETING


        Where:
                    Weintraub Building, Pelton Auditorium

        Time:
                    2:00 - 3:30 p.m.

        Contact:
                    Clinical Research Support, 206-667-4520

        Agenda:

2:00 - 2:05: Welcome

Kristi Stiffler

2:05 - 2:25: HIPAA Authorization Changes

Gerianne Sands

2:25 - 2:45: CTMS Status/PATS 2.0

Clint Vickers

2:45 – 3:05: Training Resources Update

Kersten Brinkworth

3:05 – 3:20: CPOE Update

Stephanie Langston

3:20: Questions/Closing

Kristi Stiffler
 

Friday, April 10

REGULATORY AFFAIRS OFFICE HOURS


        Where:
                Yale Bldg, J1-102

        Time:
                9:30 a.m. - 10:30 a.m.

        Contact:
                Regulatory Affairs, 206-667-1394/206-667-7167

        Agenda:
                Regulatory Affairs availability for drop-in consultations. (Click here for more information.)
 

Monday, April 13

CLINICAL RESEARCH COORDINATORS TRAINING - DAY 2


What
:

These sessions are designed primarily for those in a new role in clinical research, but some of these topics can also serve as refreshers for more experienced personnel within the Consortium – Clinical Research Coordinators, Data Coordinators, Regulatory Coordinators and Research Nurses.

More information -- including full agenda and registration form -- can be found here.

When:

The training series will be divided over three days in April 2015.

  • Day 1: April 6, 2015 (from 9:30 a.m. - 3:00 p.m.)
  • Day 2: April 13, 2015 (from 9:30 a.m. - 3:10 p.m.)
  • Day 3: April 20, 2015 (from 9:30 a.m. - 2:00 p.m.)


Contact:

Kersten Brinkworth, CRS Training Manager
 

Friday, April 17

REGULATORY AFFAIRS OFFICE HOURS


        Where:
                Fairview Bldg, LF-223

        Time:
                9:30 a.m. - 10:30 a.m.

        Contact:
                Regulatory Affairs, 206-667-1394/206-667-7167

        Agenda:
                Regulatory Affairs availability for drop-in consultations. (Click here for more information.)
 

Monday, April 20

CLINICAL RESEARCH COORDINATORS TRAINING - DAY 3


What
:

These sessions are designed primarily for those in a new role in clinical research, but some of these topics can also serve as refreshers for more experienced personnel within the Consortium – Clinical Research Coordinators, Data Coordinators, Regulatory Coordinators and Research Nurses.

More information -- including full agenda and registration form -- can be found here.

When:

The training series will be divided over three days in April 2015.

  • Day 1: April 6, 2015 (from 9:30 a.m. - 3:00 p.m.)
  • Day 2: April 13, 2015 (from 9:30 a.m. - 3:10 p.m.)
  • Day 3: April 20, 2015 (from 9:30 a.m. - 2:00 p.m.)


Contact:

Kersten Brinkworth, CRS Training Manager
 

Tuesday, April 28

CRS/IRO BROWN BAG TRAINING


        Speaker:
                    Marlisa Isom, CRS Study Implementation Manager
                    Esther Joneson, IRB Operations Manager

        Topic:
                    "Minimum Requirements for IRB Submissions"

        Where:
                    Arnold Building, M1-A303

        Time:
                    noon - 1:00 p.m.

        Contact:
                    Clinical Research Support, 206-667-4520

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