Susan Pickrel has been a Regulatory Affairs Manager at Li-Cor Biosciences since 2018. Additionally, the person has on-the-job experience at more than eight companies in the relevant field. Susan has a total work experience of 18+ years. Susan Pickrel studied at the Texas Woman's University from 2006 to 2008. Currently they live in Valley View, Texas region. You can find this professional's actual phone and email with our search.
Name variants:
Susanna Pickrel,
Susannah Pickrel,
Susanne Pickrel,
Suzanne Pickrel,
Sue Pickrel,
Susie Pickrel,
Susi Pickrel,
Susy Pickrel,
Suzie Pickrel,
Suzy Pickrel,
Sukie Pickrel,
Sarah Pickrel,
Ann Pickrel,
Anna Pickrel,
Anne Pickrel,
Annie Pickrel,
Sukey Pickrel
Last updated Jun 20, 2024
Contact Information
Workplace
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Work History
Regulatory Affairs Manager
4647 Superior St, Lincoln, NE 68504
Jul 2018 — May 2019
Manager, Pharmacovigilance
Professional development temporary assignment to transition to electronic safety reporting processes for medical devices and dietary supplements in fulfillment of FDA requirements. Subject m...
Jan 2015 — Sep 2015
Regulatory Affairs, Project Manager
Fort Worth, TX
Prepared and implemented policies, procedures and guidelines relating to developing compliant materials for promotional and advertising materials for products marketed in the US Project mana...
Nov 2010 — Jun 2012
Clinical Project Manager and Senior Clinical Research Associate and Clinical Research Associate
Implemented Phase 1, Phase 3, Phase 4, OTC Monograph, and Cosmetic Clinical Studies. Provided Clinical Study Project Management which included, but was not limited to, clinical protocol deve...
May 2005 — Nov 2010
Regulatory Affairs Associate
Fort Worth, TX
Managed and supported Regulatory Submissions – annual reports for (A)NDAs, state registrations and compliance communications, amendments/supplements, international product registration, FDA ...
Oct 2002 — May 2005
Document Assurance Manager and Document Control Supervisor and Document Control Specialist
1997 — 2000
Education
2006 — 2008
1980 — 1982
1978 — 1980
Occupations
Executive
Manager
Operations Manager
Skills
Leadership
Regulatory Affairs
Clinical Research
Gmp
Continuous Improvement
Fda
Quality Assurance
Sop
Clinical Trials
Medical Devices
21 Cfr Part 11
Quality System
Protocol
Auditing
Pharmacovigilance
Software Documentation
Management
Regulatory Submissions
Gcp
Validation
Clinical Development
Ctms
Iso 13485
Pharmaceutical Industry
Standard Operating Procedure
U.s. Food and Drug Administration
Cross Functional Team Leadership
Corrective and Preventive Action
Drug Development
Cro Management
Life Sciences
Pharmaceutics
Good Laboratory Practice
Product Launch