Job Description: We are seeking professionals with hands-on experience in the implementation, configuration, or day-to-day use of clinical trial management systems (CTMS) during human pharmaceutical trials (Phases 1–3). The goal is to better understand how these platforms are used in real-world settings, especially around workflows and privacy considerations when handling human subject data. This is a short-term advisory opportunity involving one or more 1:1 sessions where you'll walk us through your experience, key processes, and insights into how these systems are deployed and maintained. Ideal Candidates: Have worked at a company that develops CTMS software, such as: Medidata Rave CTMS Oracle Siebel CTMS Veeva Vault CTMS Bio-Optronics Clinical Conductor CTMS RealTime-CTMS (or any other similar clinical trial solution) OR have worked at a services company or CRO that implements or manages such software on behalf of pharmaceutical clients OR have experience at a healthcare provider or research site using these systems in collaboration with a trial sponsor Focus Areas: System workflows during active trials Implementation/deployment processes Key privacy and regulatory considerations (e.g., HIPAA, GDPR) Security and data access management in multi-site or international trials How to Apply: Please include a brief summary of your background, what system(s) you're familiar with, and how you’ve used or implemented them.
Keyword: Project Consultant
Price: $50.0
Project Management Client Management Customer Relationship Management English Clinical Systems CTMS Clinical Trial Clinical Trial Management System Astracore Clinical Trials eClinicalWorks
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