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Job Title: Statistical Programming Lead. Location: Northbrook, IL - Remote. Zip Code: 60062. Duration: 12 Months. Work. Fully hands-on SAS programming. Medical Affairs observational studies & post-hoc analyses. Work with 3-4 statisticians. Strict Must-Have Requirements. Strong SAS programming expertise (non-negotiable). Ability to work independently with minimal guidance. 2-5 years clinical trial or Medical Affairs experience. Strong understandin...
Clinical Trial Operations (CTO). The CTO will work remotely as a member of the Clinical Trial Team in the Study Management and Conduct Group supporting the Clinical Trial Leader (CTL), Clinical Trial Manager (CTM), and Feasibility Manager (FM). The CTO is responsible for end-to-end site management activities. In addition, may be responsible for supporting the CTL and/or CTM in leading the trial teams and is responsible for end-to-end Site Managem...
Job Title: Clinical Trial Specialist. Job Description. The Clinical Trial Specialist is responsible for coordinating the initiation and activation of new clinical trial protocols. This role involves verifying approvals from various boards, preparing study tools, and ensuring informed consent forms are properly managed. The specialist will collaborate with research nurses and physicians to confirm protocol eligibility and manage patient records. ...
Job Title: Clinical Trial Coordinator. Job Description. As a Clinical Trial Coordinator, you will play a pivotal role in the initiation and activation of new clinical trial protocols, ensuring adherence to protocol requirements and facilitating effective patient care throughout the trial process. You will collaborate with multidisciplinary teams to overcome obstacles and promote a seamless study experience. Responsibilities. Collaborate with the ...
