Liz Polvent has been working as a Director, Business Development in Vince and Associates Clinical Research, Inc. since 2012. Moreover, Liz Polvent has on-the-job experience at more than two companies in the relevant field. Liz has a total work experience of 20+ years. Liz Polvent studied at the Uc San Diego from 1999 to 2001. This professional learned English. This professional has the following certificates: Certified Clinical Research Associate (Ccra????), Certified Clinical Research Associate (Ccra®), Certified Clinical Research Associate (Ccra®) (Link), and Association of Clinical Research Professionals. Nowadays this person lives in Santa Ana, California region. Find this professional's actual e-mail and phone through our search.
Name variants:
Elizabeth Polvent
Last updated May 26, 2024
Contact Information
Last Update
Feb 1, 2016
Email
li**@yahoo.com
Location
Santa Ana, CA
Workplace
Director, Business Development
Overland Park, KS
Industry
Pharmaceuticals, Commercial Physical Research
Colleagues
Work History
Director, Business Development
Southern California
Responsible for the successful management of trial development internal and external business relationships to create a smooth transition from the development to operations.
Identifies, cul...
from Feb 2012
Clinical Research Consultant
Manage U.S. and International clinical research studies, inclusive of monitoring and/or co-monitoring of international sites if needed. Vendor management, contract negotiation and execution,...
from Apr 2005
Education
1999 — 2001
Occupations
Executive
Director
Counselor
Sales Specialist
Supplier
Operations Manager
Advisor
Services Professional
Sales Representative
Skills
Clinical Monitoring
Clinical Trials
Clinical Research
Contract Negotiation
Client Relationship Building
Business Relationship Management
Line Management
abuse liability
government proposals
Medical Writing
Project Management
Clinical Development
Clinical Study Design
Routing Protocols
protocol writing
Vendor Management
Vendor Relationships
Start-up Environment
Start-ups
Biopharmaceuticals
Gcp
Drug Development
Oncology
Protocol
Fda
Biotechnology
Regulatory Submissions
Pharmaceutical Industry
Vaccines
Drug Discovery
Life Sciences
Cro
Start Ups
Clinical Data Management
Edc
Good Clinical Practice
Standard Operating Procedure
Government Proposals
Protocol Writing
Sop
Therapeutic Areas
U.s. Food and Drug Administration
Ich Gcp
Management
Clinical Operations
Crm
Abuse Liability
Start Up Environment
Biomarkers
Infectious Diseases
Ctms
Immunology
Government Contracting
Ind
User Acceptance Testing