Clinical Scientist at Cook Group, West Lafayette, IN

Clinical Scientist at Cook Group in West Lafayette, IN. Full-time. Est. up to $160k. Apply with swipeandhired.

Posting Date 4 days ago (10/7/2026 12:00 AM) Job Location(s) West Lafayette IN United States Job Locations US-IN-West Lafayette Position Type Full Time Company Cook Research Inc. Category Clinical Overview This position is responsible for providing scientific leadership and expertise for assigned clinical studies. The Clinical Scientist independently develops clinical data strategy, designs assigned studies, and leads the analysis, interpretation, and reporting of clinical and imaging data. The role partners closely with Regulatory Affairs, Engineering, Business Units, and other cross-functional teams to advance the clinical evidence program. Responsibilities Develop clinical data strategies and independently design assigned clinical studies in collaboration with cross-functional teams (C1 study phase through handoff) Develop and maintain relationships with physician experts (e.g., National Principal Investigators, Steering Committee members) to meet clinical program objectives Lead efforts for the analysis, interpretation, presentation, and reporting of clinical and imaging data to relevant stakeholders Author and own the clinical data content within regulatory submissions (IDEs, PMAs, 510(k)s, CE Mark submissions); partner with Regulatory Affairs on submission planning and data response strategies Coordinate the presentation of information to DSMB in accordance with the DSMB Charter, including data summaries, patient summaries, study notifications, and meeting attendance For studies with an imaging component: coordinate receipt, review, and core laboratory selection, training, and management for independent imaging review Develop and execute publication and presentation plans for assigned studies in collaboration with relevant stakeholders Review and provide input on clinical study documents including CIPs, IBs, CRF specifications, IC templates, progress reports, and study overview presentations Provide support and review materials for Investigator Meetings and Site Initiation Meetings Review study data and milestones; coordinate study strategy with cross-functional stakeholders Maintain effective communication with cross-functional teams and stakeholders across the study lifecycle May provide guidance to Clinical Science Analyst staff on study-specific data tasks Qualifications Bachelor’s degree in Life Sciences, Engineering, or a closely related field required; advanced degree ( Master’s or PhD) preferred Minimum 3 years of clinical research experience, with demonstrated involvement in clinical study design and data analysis li" data-ccp-parastyle-defn='{"ObjectId":"8d7a56e0-a7b7-54f4-a484-015288fb6a82|1", "ClassId":1073872969, "Properties":[268442635, "22",469777841, "Times New Roman",469777842, "Times New Roman",469777843, "Times New Roman",469777844, "Times New