Since 2007, Lisa Hoagland has been working in Rapid Medical Research, Inc. Lisa Hoagland is an experienced Site Director with over six years of work experience. According to Lisa's CV and work profile, Lisa Hoagland has worked at more than two companies with numerous backgrounds and got various skills. Lisa attended school at the Ursuline College from 1998 to 2002. Lisa Hoagland has professional certification in Certified Clinical Research Coordinator and Association of Clinical Research Professionals. Lisa can be found in Cleveland, Ohio – where this expert is currently located. You can search for the person's phone and email. We can also provide you with detailed contact information upon request.
Name variants:
Alice Hoagland,
Elisa Hoagland,
Elizabeth Hoagland,
Melissa Hoagland
Last updated Jun 03, 2024
Contact Information
Last Update
Jul 4, 2022
Email
li**@rapidmedicalresearch.com, li**@rapidmedicalresearch.com
Location
Cleveland, OH
Company
Workplace

Colleagues
Work History
Site Director
Responsible for managing daily site operations including supervision of staff, reviewing protocols for potential participation, overseeing regulatory submissions, recruitment processes and b...
from Feb 2007
Certified Senior Clinical Research Coordinator
Clinical pharmacology research study nurse coordinator. Responsible for the direct care of study patients from screening through follow-up in phase II-IV clinical trials. Other responsibil...
2001 — 2007
Education
1998 — 2002
1993 — 1997
Occupations
Executive
Chief Executive Officer
Director
HR Specialist
Recruitment
Scientist
Clinical Research Coordinator
Health Specialist
Nurse
Coordinator
Corporate Executive
Chief Executive
Operations Manager
Researcher
Survey Researcher
Nurse Practitioner
Managers
Skills
Clinical Trials
Clinical Research
Gcp
Vaccines
Patient Recruitment
Cro
Research
Regulatory Submissions
Ctms
Protocol
Pharmaceutical Industry
Health
Medical Devices
Healthcare
Therapeutic Areas
Good Clinical Practice
Clinical Development
Ich Gcp
Pharmaceuticals
Clinical
Fda
Sop
Management