Anita Johnson Email & Phone Number | I have 20+ years of clinical research trial and data management experience in therapeutic areas of Oncology, Cardiovascular, Neuroscience and Endocrinology. I am experienced in adverse event reporting and regulatory compliance. I have participated in monitoring trials from study start-up to data lock in both a CRO and pharmaceutical setting. I have skills as a study coordinator, data manager, auditor, compliance consultant, training coordinator and I have been the lead on many projects. I have been part of a team that conducted clinical research trials worldwide and have experience with telecommuting. My degree in Health Information Administration provided me with knowledge of JCAHO, GCPs and ISDH guidelines. I have experience working with third party organizations; experience working on a global team and sharing knowledge; good analytical/problem-solving skills; computer skills with TrackWise, Microsoft Word, Excel, PowerPoint, PageMaker, MedDra coding, Veeva Vault, PPG, Trial Interactive, and InForm. My undergraduate coursework included biology, chemistry, psychology, microbiology, anatomy and physiology. I hold a Master’s of Science in Management with a focus in healthcare systems.

Anita Johnson

I have 20+ years of clinical research trial and data management experience in therapeutic areas of...
919 Spring Hill Road, Shelbyville, United States

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Anita Johnson’s Email anita.johnson@riverark.co.uk

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Anita Johnson’s Location 919 Spring Hill Road, Shelbyville, United States

Anita Johnson’s Current Industry Riverark

Anita Johnson’s Prior Industry Syneos Health Clinical Solutions | Eli Lilly

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Work Experience

Riverark

Principal GCP Consultant

2021-05-01 00:00:00 - Present

Syneos Health Clinical Solutions

Trial Master File Lead

2019-05-01 00:00:00 - 2021-05-01 00:00:00

Eli Lilly

Medical Quality Auditing and Compliance

2012-04-01 00:00:00 - 2014-12-01 00:00:00

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FAQ About Anita Johnson

Anita Johnson is located at
919 Spring Hill Road, Shelbyville, United States

Anita Johnson is a I have 20+ years of clinical research trial and data management experience in therapeutic areas of Oncology, Cardiovascular, Neuroscience and Endocrinology. I am experienced in adverse event reporting and regulatory compliance. I have participated in monitoring trials from study start-up to data lock in both a CRO and pharmaceutical setting. I have skills as a study coordinator, data manager, auditor, compliance consultant, training coordinator and I have been the lead on many projects. I have been part of a team that conducted clinical research trials worldwide and have experience with telecommuting. My degree in Health Information Administration provided me with knowledge of JCAHO, GCPs and ISDH guidelines. I have experience working with third party organizations; experience working on a global team and sharing knowledge; good analytical/problem-solving skills; computer skills with TrackWise, Microsoft Word, Excel, PowerPoint, PageMaker, MedDra coding, Veeva Vault, PPG, Trial Interactive, and InForm. My undergraduate coursework included biology, chemistry, psychology, microbiology, anatomy and physiology. I hold a Master’s of Science in Management with a focus in healthcare systems.