Edith Mitchell

Edith Mitchell is a clinical research coordinator who has been with InterVenn Biosciences since November 2014. Edith is responsible for obtaining informed consent from patients, ensuring that samples are collected and delivered correctly, and maintaining relationships with external entities such as the FDA and clinical trial sponsors. Edith is also a subject matter expert for onboard training of newly hired coordinators and has created standard operating procedures for department study tasks.

Edith Mitchell studied Biomedical Sciences at Florida State College at Jacksonville, before going on to complete a Monitor Technician program at the Mayo Clinic. Edith has also gained a certification in GCP for Clinical Trials with Investigational Drug and Devices from CITI Program, A Division of BRANY.


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InterVenn Biosciences

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InterVenn Biosciences utilizes a proprietary high-throughput glycoproteomic interrogation platform using artificial intelligence and mass spectrometry for next-gen precision medicine. The company is working to find new solutions in ovarian, pancreatic, liver, prostate, and kidney cancer, together with applications from the Vista suite of solutions for treatment and monitoring, immune profiling, patient stratification, and disease progression.


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