Megan Chamberlain
About Megan Chamberlain
Megan Chamberlain is a Clinical Trial Associate at Insmed Incorporated, where she has worked since 2021. She has extensive experience in clinical research, having held various roles across multiple organizations and focusing on oncology and other therapeutic areas.
Work at Insmed
Megan Chamberlain has been employed at Insmed Incorporated as a Clinical Trial Associate since 2021. In this role, she contributes to the management and coordination of clinical trials, ensuring compliance with regulatory requirements and company protocols. Her position is based in Bridgewater, New Jersey, where she has gained valuable experience over the past three years.
Previous Experience in Clinical Research
Prior to her current role, Megan worked at Mitsubishi Tanabe Pharma Development America as a Clinical Operations Consultant for seven months in 2020. She also held positions at BeiGene as an In House CRA III/Clinical Trial Associate and at Sanofi as an In House CRA/Clinical Project Associate. Her earlier experience includes roles at Moffitt Cancer Center, where she served as a Research Coordinator and later as a Clinical Research Coordinator.
Education and Expertise
Megan Chamberlain earned a Bachelor of Science in Psychology from Liberty University, completing her studies from 2011 to 2014. She furthered her education by obtaining a Master of Science in Management in Healthcare from Southern New Hampshire University, which she completed in 2022. Her educational background supports her expertise in clinical research and operations.
Clinical Research Specialization
Megan has extensive experience in various phases of clinical trials, including phase Ib, II, and III. She has worked on clinical trials across multiple therapeutic areas such as Sarcoma, Multiple Myeloma, Breast Cancer, and Rare Diseases, including conditions like Parkinson's and Cystic Fibrosis. Her clinical research career began at Moffitt Cancer Center, focusing on Oncology.
Technical Skills in Clinical Trials
Megan Chamberlain possesses extensive experience with electronic data capture systems and clinical trial management tools. She is proficient in using platforms such as CTMS, Medidata, and Veeva Vault, among others. Her technical skills enhance her ability to manage clinical trials effectively and ensure accurate data collection and reporting.