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Jeremiah Rehm

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Jeremiah Rehm
Jeremiah Rehm
Clinical Solutions Specialist

Jeremiah has been an innovator in Life Sciences for more than 13 years -- the last 8 of those designing and maintaining Clinical Trial Management Systems. Prior to joining Bioclinica, he was a technology consultant and led the product management team for eClinical products acquired by Bioclinica. One of Jeremiah's specialties is in the use of Microsoft applications to consolidate and analyze operational study information, including translation of this data into meaningful performance metrics.

Blogs

Regulatory authorities require clinical trial progress to be monitored. The site visit report, known as the Monitor Visit Report (MVR), is where sponsors provide evidence that all regulated activities have been completed along with documentation of the outcome. These reports are open to regulatory inspection at any time during a study, as well as after, and even post product approval.

CTMS and MVR, Across the Great Divide
As anyone in pharma knows, our industry is undergoing major change; clinical trials are rapidly evolving and eClinical technologies are becoming more sophisticated by the day. Meanwhile site monitoring continues to be one of the most critical, costly, and labor-intensive activities in a clinical trial. Looking for a better way to address this, many organizations have made the switch from conventional CTMS to the "Microsoft Office-Smart" model.

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Leader in Clinical Trial
Management Solutions

Successful clinical trials require the ability to see key details and uncover hidden insights. Bioclinica utilizes science and technology to bring clarity to clinical trials, helping companies to develop new life-improving therapies more efficiently and safely.

Dr Joby John chairing a panel discussion tomorrow 8am at #DIA2019 on ways to improve connectedness of clinical data… https://t.co/BPzi1geKsv
Bioclinica (14 hours ago)
Meet the Bioclinica team at DIA Booth 1831. #DIA2019 https://t.co/pvvdiqJz32 https://t.co/tx4PLDIrMm
Bioclinica (16 hours ago)
We’re at #DIA2019. Visit us at booth #1831 to learn more about our rapidly growing services and meet face to face… https://t.co/rK7V1Aclov
Bioclinica (19 hours ago)
Learn about When EDC is not enough: Automating multi-country data collection and complete workflows at #DIA2019! Ja… https://t.co/zJfytNpz82
Bioclinica (1 week ago)
In San Diego for #DIA2019? Visit us at booth #1831 and meet face to face with our team to learn more about our rapi… https://t.co/T4U4oNXlxo
Bioclinica (2 weeks ago)
We're celebrating International #NASH Day to help raise awareness about non-alcoholic steatohepatitis & fatty liver… https://t.co/16PfGbzeaS
Bioclinica (2 weeks ago)

Latest Blogs:

Medical Imaging of Non-Alcoholic Fatty Liver Diseases in Clinical Trials
EDC Provider Selection
Site Payments Solutions
Nonalcoholic steatohepatitis (NASH) development programs
Dr. Joby John
Transformational Trends in Investigator Site Payments
Clinical Supply Chain Success: Leveraging Technology
Blood pressure monitor
Prescription box