
Fortune Ngumezi
I have a total of eight years of experience in the clinical trial... | Houston, Texas, United States
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Fortune Ngumezi’s Emails fo****@dm****.com
Fortune Ngumezi’s Phone Numbers No phone number available.
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Fortune Ngumezi’s Location Houston, Texas, United States
Fortune Ngumezi’s Expertise I have a total of eight years of experience in the clinical trial field, but four years of experience as a W2 clinical research monitor or CRA. I also have extensive knowledge of therapeutic areas such as oncology, cardiovascular, metabolic, and respiratory disorders. My home is located in Houston, Texas, and I live 20 min from Bush Intercontinental and Hobby airport. I earned a Bachelor of Science degree in medical case management from the University of Davenport. The core classes in this bachelor program have prepared me for my career in the clinical research field, especially in understanding the wide range of medical terminologies and therapeutic areas. The curriculum includes pathology, pharmacology, biostatistics, behavioral science, microbiology, and immunology. My academic background and knowledge of clinical protocols compliance make me an ideal candidate for any CRA roles. I am a motivated and focused leader who displays a high level of accuracy and attention to detail. I possess excellent communication and interpersonal skills and the ability to build and maintain relationships with diverse groups of colleagues, clients, and patients. With superior time management, problem-solving, organization, and multitasking skills, I can manage high-priority assignments with ease. I apply an initiative to complete tasks in fast-paced, changing work environments. I’ve gained recognition for my innovation, confidence, and ability to meet strict deadlines consistently. As a trustworthy, resourceful, and sharp healthcare professional, I know that I will be a significant asset to your organization.
Fortune Ngumezi’s Current Industry Dm Clinical Research
Fortune
Ngumezi’s Prior Industry
Savient Pharmaceuticals
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Chiltern
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Tranquil Clinical Research
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Dm Clinical Research
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Work Experience

Dm Clinical Research
Quality Assurance Lead
Wed Sep 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Tranquil Clinical Research
Clinical Research Associate
Mon Feb 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Aug 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)
Chiltern
Clinical Research Associate
Tue Jul 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed May 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time)
Savient Pharmaceuticals
Clinical Trial Coordinator
Mon Feb 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Dec 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time)