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    Brenda Breitz

    Sr. Patient Safety Specialist/Patient Safety Program Coordinator at Novartis

    Brenda Breitz is a highly experienced Registered Nurse with over 20 years of expertise in clinical trials and research. Her skill set encompasses various aspects of clinical trial management, from study initiation to data closure, monitoring, safety training, Disease Process education, and interaction with legal teams. She is an independent, detail-oriented professional dedicated to ensuring the accuracy and depth of research, with a focus on producing precise and easily understandable reports. Brenda excels in communicating complex medical information to diverse audiences, including Legal, Regulatory Affairs, Sales, Marketing, and Specialty Groups. She is known for upholding high standards in research and reporting, making her a valuable resource for interdisciplinary teams seeking medical knowledge and education.

    Brenda Breitz's educational background includes a B.A. in Sociology from The King's College, Briarcliff, and an A.A.S. in Applied Sciences with a focus on becoming a Registered Nurse from Morris County Community College.

    In terms of professional experience, Brenda has held notable positions in various organizations. She previously served as a Patient Safety Program Coordinator at Novartis within PRA Health Sciences, a Medical Affairs Associate at Warner Chilcott, a Clinical Data Manager at Novartis, a Drug Safety Associate at Sentrx, a Clinical Safety Scientist at Novartis, a Drug Safety Associate at Novartis Pharmaceuticals, Inc., a Clinical Research Associate at The Hardardt Group, a Study Coordinator, and CRA at MED CHEM CORP, and a Clinical Data Manager at MEADOX MEDICALS, INC.

    Brenda Breitz
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    Location

    Gladstone, New Jersey, United States