We found the following information about Tina Erhardt at Scl Health, where this expert has worked as a Director of Research - Mt Region since 2017. Tina's total work experience is over seven years, during which time Tina had at least five jobs at different companies to develop professional skills. Tina studied at the Walden University from 2011 to 2013. This expert received the following certifications: Protecting Human Research Subjects, Shipping of Category A, Infectious Substance Affecting Humans Category B, Biological Substance, and Southwest Oncology Group Clinical Trials Training Course. Currently, Tina is located in Billings, Montana. You can contact with Tina by searching for phone number or email or find further information by requesting access to Tina's additional details from SoftwareOfficial.
Name variants:
Albertina Erhardt,
Augustina Erhardt,
Celestine Erhardt,
Christine Erhardt,
Clementine Erhardt,
Ernestine Erhardt,
Justina Erhardt,
Martina Erhardt
Last updated Jun 21, 2024
Contact Information
Last Update
Jul 12, 2022
Email
ti**@sclhealth.org, ti**@gmail.com
Location
Billings, MT
Company
Workplace
Colleagues
Work History
Director of Research - Mt Region
500 Eldorado Blvd SUITE 4300, Broomfield, CO 80021
Director of Research - MT Region
Nov 2017 — Apr 2018
Oncology Clinical Research Manager
Oncology Clinical Research Manager at St. Vincent Frontier Cancer Center
Mar 2015 — Apr 2018
Regional Director - Clinical Research Operations
500 Eldorado Blvd SUITE 4300, Broomfield, CO 80021
from Jan 2018
Clinical Research Associate
Clinical research and data management activities including identifying potential study patients, ensuring participant selection is congruent with phase criteria, obtaining informed consent, ...
Feb 2012 — Mar 2013
Education
2011 — 2013
2009 — 2011
Occupations
Executive
Region Manager
Chief Research Officer
Health Specialist
Hospital Care Professional
Research Manager
Doctor
Oncologist
Area Manager
Managers
Chief Executive
Health Professional
Health Practitioner
Medical Practice Professional
Medical Practitioner
Skills
Clinical Trials
Oncology
Clinical Research
Cro
Gcp
Cancer
Oncology Clinical Research
Protocol
Ich Gcp
21 Cfr Part 11
Ctms
Clinical Data Management
Edc
Informed Consent
Clinical Development
Sop
Infectious Diseases
Biotechnology
Lifesciences
Pharmaceutical Industry
Regulatory Submissions
Gmp
Biology
Chemistry
Adverse Event Reporting
Ctcae
Sae Reconciliation
Clinical Pharmacology
Research Ethics
Biologics
Irb
Iec
Fda
Clinical Research Associates
Regulatory Requirements
Regulatory Documentation
Meddra
Pharmacokinetics
Pharmacology
Drug Safety
Ich Guidelines
Medidata
Hematology
Inform
Clinical Study Design
Data Management
Regulatory Affairs
Patient Recruitment
Sop Development
Biomarkers