Fortrea

Job Overview: Perform data management activities such as clinical data review, query generation / resolution and reconciliation activities to support the Lead Data Reviewer/LDM with the delivery of cl

Job Overview: Serve as a member of the project team with primary responsibility for coordinating the clinical data review, query generation / resolution and reconciliation activities to support the Da

Summary of Responsibilities: Assists Proposal Managers with all aspects of the appropriate proposal process (text, quote, budget, and/or response to Requests for Information [RFIs]) (i.e., collating d

Job Overview: Manage ‘Client’ or ‘Project’ specific PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials an

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: Provide Statistical Programming support for clinical trial projects. Develop, validate, and maintain SAS programs and outputs for the management, analysis, and reporting o

Job Overview: Scientific Writer with strong expertise in material science, analytical chemistry, and chemical principles (organic and inorganic) as applied to pharmaceutical formulation, manufacturing

Job Overview: The Associate Medical Data Review Manager is an important member of the Global Medical Review Team with responsibility for execution of key Central Medical Review activities within the C

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: To complete other duties/activities as assigned by study management team, but not limited to: Manage clinical systems and access management. Manage study documents and sup