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Job Overview: Assist in the development and implementation of solutions to DM service issues and concerns regarding Medidata RAVE, Oracle Inform, CRF Design, and Data Capture or imaging activities, in

Job Overview: Responsible for performing TMF review of electronic Trial Master Files (eTMF), Trial, Country, and Site artifacts for clinical studies in support of sponsors services contracts and inter

Job Overview: Responsibility for delivering EDC design and specifications within the scope of assigned projects to achieve project integrity and the delivery of on-time, quality data. Document and mai

Summary of Responsibilities: Draft, review, negotiate, and finalize Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, and related site contract documentation. Coordinate with s

Summary of Responsibilities: Draft, review, negotiate, and finalize Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, and related site contract documentation. Coordinate with s

Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the adverse events process which may include safety data collected from clinical trials a

Job Overview: The Central Monitoring Specialist is responsible for the execution of key Central monitoring (Site, subject and study level review as applicable) activities and in assisting the executio

Job Overview: • Assist with the overall Safety system implementation, support, configuration, and Migration related activities. • Responsible for providing this service to clients either as a support

Job Overview: It is the responsibility of the post holder to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost-effective manner. The individua

Job Overview: Assist with the overall Safety system implementation, support, configuration, and migration related activities. Responsible for providing this service to clients either as a support func