Trial Disclosures 1
Introduction to Trial Disclosures
This one-of-a-kind course provides background perspective, and technical skill sets for facilitating workflow and summarizing data to meet global trial disclosure requirements.
This new regulatory requirement has the industry catching up to maintain compliance. Outsourcing is increasing and the skills required to meet disclosure requirements are in high demand. This course will provide hands-on experience with writing and reporting to global registries with a focus on Clinicaltrials.gov (US) and EudraCT (EMA). Students will learn the legal and ethical basis for disclosure of clinical trial protocol and results, a comprehensive overview of Clinicialtrials.gov and EudraCT, processes for protocol and results summarization and release for Clinicaltrials.gov and EudraCT, review of other mandatory international registries and systems, and workflow for operationalizing clinical trial disclosures.
Students will be tested on their ability to draft and submit a disclosure. This exercise will prepare them to be a functional member of the clinical trial disclosure team within a CRO or pharmaceutical industry.
Who Should Take This Course
This is an ideal course for the detail-oriented, regulatory-focused and compliance-minded scientist or student with a pharmaceutical industry focus.
Duration and Prerequisites
A total of 18 weeks is needed for completing the program.
Education and/or Experience
Work experience must be in a full time, paid role. Paid intern, co-op or any other course work cannot be applied toward the work experience requirement.
You must have seven years of on-the-job experience in one or more of the areas of the Disclosures course content.
If you have completed a degree* from a college, university or technical school with accreditation accepted by MMSU, part of the two-year experience requirement will be waived as follows (only one of these waivers may be claimed):
Assessments
Knowledge checks will be performed through a quiz in every session. Evaluation of written reports will be performed through multiple assignments/exercises and will conclude with a final examination. A minimum of 75% is required to pass the final examination.
* Degrees or diplomas from educational institutions outside the United States must be equivalent to degrees from U.S. educational institutions.
Course Fee
$2,125 USD
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Meet Our Instructors
Mr. Joe Archer is the Associate Director, Trial Disclosure Services, and instrumental in the launch and growth of the clinical trial disclosure business at MMS. Mr. Archer has over 25 years of experience in clinical research and is a Subject Matter Expert of processes and systems related to the reporting of clinical trial information to ClinicalTrials.gov, EudraCT, and additional registries globally. Prior to holding this role, Mr. Archer was Senior Manager, Clinical Trial Disclosures at GlaxoSmithKline from 2007 to 2011 where he led the development and oversight of systems, processes, quality controls and compliance of clinical disclosure reporting of the company’s protocol and results summary information.
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