Job Description
Strong knowledge of CRO compliance and Clinical Trial LifecycleComprehensive knowledge of key technology platforms used in clinical trialsAbout Our Client
The hiring organization is a next-generation Contract Research Organization (CRO) that accelerates clinical trials for biotech companies by combining deep industry expertise, advanced technology platforms, and access to a global patient network.
Job Description
Understand CRO business processes end-to-end, including protocol design, clinical trial execution, data management, and regulatory compliance.Possess deep knowledge of clinical trial technology stack, especially EDC systems like Medidata Rave, Veeva Vault, and emerging platforms such as Zelta, Clinion, Viedoc.Anticipate and evaluate emerging technologies to future-proof operations, including decentralized trials and eSource solutions like Florence eBinder.Design and refine a long-term technology roadmap aligned with organizational goals and industry trends.Build and maintain strategic relationships with technology vendors, negotiate licensing agreements, and ensure platform interoperability.The Successful Applicant
Strong understanding of CRO operations and regulatory frameworks, including clinical trial lifecycle and compliance standards (ICH-GCP, FDA, EMA).Proven expertise in clinical technology platforms, especially EDC systems like Medidata Rave and Veeva Vault, with awareness of emerging solutions.Ability to develop and execute a forward-looking technology roadmap that aligns with business objectives and industry trends.Excellent vendor management and negotiation skills to build strategic partnerships and maintain licensing agreements across platforms.Strategic mindset with the ability to anticipate technological shifts, drive innovation, and ensure scalability and interoperability of systems.
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