Meet our people.

At Syner‑G, you gain a hands‑on partner with deep scientific expertise, providing continuous, collaborative problem‑solving throughout development.

Bryan

Abney

MS

VP, Quality & Compliance

Drew

Barlow

MPH

SVP, Head of Regulatory Partnerships

Matt

Brown

MBA

VP, Program Management & M&A

Ed

Ciolkowski

PhD

VP, Pharmaceutical Development, Small Molecule

John Paul

Cunniffe

Director, Facilities Engineering

Caroline

Drucker

PhD, RAC

Principal Manager, Medical Writing

Candace

Farley

Prosci

Director, Organizational Change Management & Development

Raymond

Forslund

PhD, MBA

EVP, Head of Product Development

Kelley

Gillespie

Senior Director, Quality and Compliance

Jeff

Golden

VP, Regulatory Operations

Judy

Hauser

PhD

VP, Regulatory Affairs, CMC

Velvizhi

Heine

PhD, RAC

Vice President, Regulatory CMC

Brian

Hockin

Lean Six Sigma Black Belt

Sr. Director, Business Excellence

Richard

Inman

Sr. Director, GMP & Operational Readiness

Nathan

Jack

Sr. Program Manager, Business Excellence

Jennifer

Kilroy

PhD, MBA

SVP, Head of Strategy & Transformation

Anuj

Kumar

PhD

VP, Pharmaceutical Development

Liza

Lamb

Sr. Director, Process & Automation – Global

Nate

Lawson

Director, Technical Operations

Donna

Little

MS

VP, Regulatory Affairs, CMC

Sarah

Mohs

VP, Regulatory Affairs

Priscilla

Pingrey

Director, Engineering Programs

Stacy

Plum

PhD

SVP, Pharmaceutical Development

Kasturi

Puranam

PhD

Senior Manager, Medical Writing

Dan

Ramsey

MS

EVP, Head of Technical Operations & Delivery Infrastructure

Michael

Reardon

Sr. Director, Pharmaceutical Development

Libby

Russell

PhD

VP, Pharmaceutical Development

Jay

Samudralwar

PhD

Vice President, Regulatory CMC

Nancy

Smith

PhD, RAC

SVP, Medical Writing Services

Morgan

Watson

MS

Director, Product Lifecycle Management

Maria

Wik

MS, PhD

VP, Pharmaceutical Development

Marieke

Zhao

PhD

VP, Pharamceutical Development

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