With work experience over 25 years, Sara Rice is nowadays working at Swog - Leading Cancer Research. Together which is based in 101 as a Protocol Coordinator I. Sara received his education from 2014 to 2016 at the University of Phoenix. Sara Rice is located in Lytle, Texas. To contact directly with Sara, you can search for their phone number or e-mail address or get exhaustive info by requesting access to this expert's further details.
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Sarah Rice
Last updated Jun 17, 2024
Contact Information
Last Update
Jul 12, 2022
Email
ce**@yahoo.com
Location
Lytle, TX
Workplace
Colleagues
Work History
Protocol Coordinator I
2611 southwest 3Rd Ave, Portland, OR 97201
Coordinate all aspects of Lung-MAP, a multi-sub-study biomarker-driven lung cancer clinical trial, from initial concept to study completion. Serve as a liaison to the Lung-MAP public/private...
Oct 2018 — Jul 2019
Data Manager
607 Camden St SUITE 100, San Antonio, TX 78215
Entry of data into Electronic Data Capture systems within parameters set forth by Protocol and Sponsor requirements. Verify the data entered is consistent with Subject clinical notes, source...
May 2017 — Oct 2018
Clinical Research Coordinator
7706 Golden Triangle Dr, Eden Prairie, MN 55344
ThreeWire, a leader in clinical trial recruitment and direct-to-patient marketing, has been helping pharmaceutical, medical device and biotech companies achieve their patient recruitment, en...
Sep 2016 — May 2017
Qc Monitor
Conducted internal clinical trial related quality control checks during critical phases of the trial activities in the clinical research unit.
Performed quality control checks of data and ...
Oct 2012 — Oct 2013
Supervisor Medical Data Operations
50 Binney St, Cambridge, MA 02142
Jun 2001 — Jul 2012
Education
2014 — 2016
from 1993
Occupations
Coordinator
Doctor
Oncologist
Managers
Medical Practice Professional
Medical Practitioner
Skills
Clinical Trials
Gcp
Sop
Fda
Cro
Clinical Research
Pharmaceutical Industry
Data Management
Ich Gcp
Protocol
Edc
Ctms
Clinical Development
Biotechnology
Quality Assurance
Clinical Data Management
Oncology
Regulatory Affairs
Clinical Study Design
21 Cfr Part 11
Regulatory Submissions
U.s. Food and Drug Administration
Standard Operating Procedure
Good Clinical Practice
Metrics
Electronic Data Capture