Marilyn Van Kerkhoven
About Marilyn Van Kerkhoven
Marilyn Van Kerkhoven is a Senior Clinical Site Manager and Senior Study Start Up Specialist at Bristol-Myers Squibb in Melbourne, Victoria, Australia, with over 19 years of experience in clinical trials and oncology.
Company
Marilyn Van Kerkhoven currently works at Bristol-Myers Squibb. She has been with the company for over 19 years, starting her tenure in January 2004. Based in Melbourne, Victoria, Australia, she holds the position of Senior Clinical Site Manager and Senior Study Start-Up Specialist. Bristol-Myers Squibb is recognized for its innovative approach in pharmaceuticals, particularly in areas like oncology and immunology.
Title
Marilyn Van Kerkhoven serves as a Senior Clinical Site Manager and Senior Study Start-Up Specialist. Her role involves overseeing clinical site operations and facilitating the start-up phase of clinical trials. Her responsibilities include managing HREC/RGO submissions and creating Participant Information and Consent Forms (PICF).
Education and Expertise
Marilyn Van Kerkhoven studied Medical Science at UNSW, where she earned a Master's degree from 2002 to 2005. Additionally, she holds a Post Graduate Diploma in Oncology Nursing from La Trobe University. Her educational background provides a strong foundation for her expertise in clinical trials, particularly in oncology and biotechnology.
Background
With a robust background in oncology, Marilyn Van Kerkhoven contributes significantly to the development and management of cancer-related clinical trials. Her expertise in Good Clinical Practice (GCP) ensures that clinical trials adhere to ethical and scientific quality standards. Her experience in biotechnology enhances her understanding of biological processes and technologies used in drug development.
Specialization in Clinical Trials
Marilyn Van Kerkhoven specializes in the management of clinical trials within the pharmaceutical industry. With over a decade of experience in HREC/RGO submission and PICF creation, she plays a key role in preparing and executing clinical trials. Her comprehensive expertise ensures the successful initiation and management of clinical studies, adhering to high standards of quality and ethics.