Kakali Hossain, Mbbs, Ccrc
About Kakali Hossain, Mbbs, Ccrc
Kakali Hossain is a Clinical Research Associate with extensive experience in managing clinical research protocols. She has worked with various organizations, including Aimmune Therapeutics and Acerta Pharma, and possesses strong skills in project management and regulatory compliance.
Work at Aimmune Therapeutics
Kakali Hossain has been employed at Aimmune Therapeutics as a Clinical Research Associate since 2019. In this role, she has accumulated five years of experience in managing clinical research projects. Prior to her current position, she worked as a Senior Clinical Trial Assistant at Aimmune Therapeutics from 2017 to 2019, where she contributed to various clinical trials. Her responsibilities included ensuring patient safety, data accuracy, and adherence to project timelines.
Previous Experience in Clinical Research
Kakali Hossain has a diverse background in clinical research, having worked in several prominent organizations. She served as a Clinical Trial Assistant at Acerta Pharma B.V. for five months in 2017. Additionally, she worked at Stanford University Hospital as a Clinical Research Coordinator in the Department of Gastroenterology and Hepatology for five months in 2010. Her experience also includes six years at West Coast Research LLC as a Clinical Research Coordinator from 2010 to 2016 and a four-month stint as a Clinical Trial Associate Consultant at Genentech in 2016.
Education and Expertise
Kakali Hossain holds a Bachelor of Medicine and Bachelor of Surgery from Mymensingh Medical College in Bangladesh. She furthered her education at the University of California, Santa Cruz, where she achieved a specialization in Clinical Trial Design and Management. Her educational background supports her extensive experience in managing complex clinical research protocols and her in-depth knowledge of FDA regulations and ICH/GCP guidelines.
Skills in Clinical Research
Kakali Hossain demonstrates strong management, interpersonal, and organizational skills in clinical research settings. She is experienced in communicating effectively with both internal and external stakeholders involved in clinical research projects. Her skills include ensuring patient well-being and safety, maintaining data accuracy, and managing project timelines, which are critical for the successful execution of clinical trials.