Jennifer Klesh
About Jennifer Klesh
Jennifer Klesh is the Associate Director at Bristol-Myers Squibb in New Jersey, specializing in business solutions for IDMP and eCTD with over 20 years of experience in regulatory affairs and document management.
Current Position at Bristol-Myers Squibb
Jennifer Klesh holds the position of Associate Director at Bristol-Myers Squibb in New Jersey. Her tenure with the company spans multiple roles, demonstrating her longstanding commitment and expertise in regulatory affairs and document management.
Career Progression at Bristol-Myers Squibb
Jennifer Klesh began her career at Bristol-Myers Squibb as a Document Publisher (Contractor) from 2001 to 2002. She transitioned to a full-time Document Publisher from 2002 to 2004. Following this, Jennifer served as a Dossier Expert from 2004 to 2015, and then as a Regulatory Capability Strategist from 2015 to 2018. Her consistent career growth within the company highlights her dedication and expertise in regulatory capabilities and document management.
Educational Background and Qualifications
Jennifer Klesh completed a Master of Business Administration (MBA) in Leadership at Liberty University from 2013 to 2017. Earlier, she earned a Bachelor's degree in Visual Communications from the University of Pittsburgh, where she studied from 1998 to 2001. She also has a background in Graphic Design, having studied at La Roche College from 1997 to 1998.
Specialization in Regulatory Affairs and Document Management
Jennifer Klesh specializes in business solutions for IDMP (Identification of Medicinal Products) and eCTD (electronic Common Technical Document). Her over 20 years of experience in regulatory affairs and document management underscore her deep expertise and capability in these specialized areas.
Transition from Visual Communications to Regulatory Affairs
Jennifer Klesh transitioned from a background in visual communications and graphic design to a career in regulatory affairs. This shift showcases her adaptability and skill in acquiring new expertise, enabling her to excel in document management and regulatory capabilities at Bristol-Myers Squibb.