Denise R.

Denise R.

Director, Pharmacovigilance & Drug Safety @ Geron

About Denise R.

Denise R. serves as the Director of Pharmacovigilance & Drug Safety at Geron Corporation, a position she has held since 2024. With extensive experience in clinical operations and management, she has previously worked in various roles at Kolon TissueGene, Inc., Geron Corporation, and Lundbeck Pharmaceuticals.

Current Role at Geron Corporation

Denise R. serves as the Director of Pharmacovigilance & Drug Safety at Geron Corporation. She has held this position since 2024, contributing to the company's commitment to patient safety and regulatory compliance. In this role, she oversees the pharmacovigilance processes and ensures that drug safety practices align with industry standards. Her responsibilities include monitoring adverse events and implementing risk management strategies.

Previous Experience at Geron Corporation

Before her current role, Denise R. worked at Geron Corporation as the Director of Clinical Science from 2021 to 2024. During this time, she played a significant role in the design and execution of clinical studies. Her leadership in clinical science helped advance the company's research initiatives and fostered collaboration among clinical teams.

Experience at Kolon TissueGene, Inc.

Denise R. has experience at Kolon TissueGene, Inc., where she served as the Senior Clinical Program Manager from 2017 to 2021 and as the Senior Clinical Trial Manager from 2016 to 2017. In these roles, she managed clinical trials and contributed to the development of clinical study documentation, including protocols and investigator's brochures.

Background in Clinical Operations

Denise R. has a strong background in clinical operations, having worked as a Clinical Operations Manager at Lundbeck Pharmaceuticals from 2009 to 2015. Her experience in this position involved overseeing complex clinical projects and ensuring operational efficiency. She demonstrated leadership in managing clinical programs and coordinating independent data monitoring.

Skills and Expertise in Clinical Research

Denise R. possesses demonstrated skills in various aspects of clinical research, including protocol development, investigator's brochure creation, and informed consent documentation. Her expertise extends to independent data monitoring coordination, which is essential for maintaining the integrity of clinical trials. Additionally, she has a proven track record in direct line management and resourcing, showcasing her leadership and team-building capabilities.

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