L

Libette Luce's
email & phone

Current Position:

Vice President, Head of Regulatory Affairs at Akero Therapeutics

Experience:

24 years

Location:

Branchburg, New Jersey, United States

How to contact Libette Luce

emaill**@akerotx.com
phone+1-***-***-5911
LinkedIn

Work Experience

Vice President, Head of Regulatory Affairs at Akero Therapeutics

May 2022 - Current

Vice President, Head of Regulatory Affairs at Innocoll Biotherapeutics

May 2021 - May 2022

Executive Director Global Regulatory Affairs at Bausch Health Companies Inc.

Oct 2020 - May 2021

Senior Director Global Regulatory Affairs at Bausch Health Companies Inc.

Sep 2017 - Oct 2020

Director Global Regulatory Affairs at Bausch Health Companies Inc.

Dec 2014 - Sep 2017

Senior Manager US Regulatory Affairs at Allergan

Apr 2013 - Nov 2014

Senior Manager Global Regulatory Affairs at Amarin Corporation

Jan 2012 - Mar 2013

Manager Global Regulatory Affairs at Forest Laboratories (now Allergan)

Jun 2009 - Jan 2012

Associate Global Regulatory Affairs at Roche

Mar 2006 - Jun 2009

Field Sales Representative at Novartis

Sep 2004 - Mar 2006

Associate Global Regulatory Affairs at Schering-Plough Research Institute

Aug 2002 - Sep 2004

Libette Luce started working in 2002, then the employee has changed 8 companies and 8 jobs. On average, Libette Luce works for one company for 2 years 1 month.

Education

Master of Arts - MA at Seton Hall University

Bachelor of Arts - BA at University of Miami

High School Diploma at Dwight-Englewood School

Skills

Pharmacovigilance, Diabetes, eCTD, Oncology, CMC, Neurology, Standard Operating Procedure (SOP), Workload Prioritization, CRO, Regulatory Compliance, Pharmaceutical Industry, Business Knowledge, CMC Regulatory Affairs, Drug Development, NDA, Regulatory Requirements, Endocrinology, Biologics, MHRA, CRO Management, GxP, Regulatory Affairs, U.S. Food and Drug Administration (FDA), Abbreviated New Drug Application (ANDA), Clinical Development, Common Technical Document (CTD), Biotechnology, ICH-GCP, GCP, Regulatory Submissions, U.S. Title 21 CFR Part 11 Regulation, Clinical Trials, Clinical Operations, Dermatology, SOP, Pharmaceutics, Good Clinical Practice (GCP), Cross-functional Team Leadership, IND, Regulatory Filings, Therapeutic Areas, GMP, Quality Assurance, Medical Affairs, FDA, EMA, Biopharmaceuticals, 21 CFR Part 11, International Regulations

Frequently Asked Questions

What is Libette Luce's minimum period of employment in the companies?

Libette Luce's minimum period of employment in various companies is 7 months.

What is Libette Luce's average duration of employment for different companies?

On average, Libette Luce works for one company for 2 years

What industries has Libette Luce worked in?

Libette Luce works in the Biotechnology. Previously, Libette Luce worked in the Pharmaceuticals.

What positions has Libette Luce held before?

Previously, Libette Luce worked as a Vice President, Head of Regulatory Affairs, and Executive Director Global Regulatory Affairs, and Senior Director Global Regulatory Affairs, and Director Global Regulatory Affairs, and Senior Manager US Regulatory Affairs.

How do I contact Libette Luce?

Libette Luce's email address is l**@akerotx.com, phone number is +1-***-***-5911. Sign up to get contact details.

Who is the President/CEO/Director of the Akero Therapeutics?

The President/CEO/Director of the Akero Therapeutics is Thomas Quinn

Who are Libette Luce's peers at other companies?

Libette Luce's peers at other companies are Catherine Burgess and Elvis Osei Tutu and Marsha Miller
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