Entry Clinical Trials Proposal Writer Medpace, Inc.Entry Clinical Trials Proposal WriterCincinnati, OhioWhen you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration. This position will work closely with the operations and business development teams to prepare proposals for new business in the pharmaceutical industry with the opportunity to develop strategical content at the intersection of science, operations and finance while developing your career.
Spring 2027 Clinical Trials Feasibility & Proposals Internship Medpace, Inc.Spring 2027 Clinical Trials Feasibility & Proposals InternshipCincinnati, OhioQualifications: High school diploma or equivalent; Bachelor's degree in progress, in a Life Sciences field; Knowledge of MS Word, Excel, and PowerPoint; Knowledge and organizational skills to perform day-to-day departmental support activities (i.e., shipping, archiving, filing, departmental meeting minutes); Demonstrated ability to maintain applicable database systems; Demonstrated ability to adequately communicate (written and oral) with other employees as necessary; and. Coordinate and provide summary for departmental meetings/conference calls as and when required; Maintain database/spreadsheets and compile reports as necessary to facilitate tracking/documentation of departmental activities; Conduct quality control reviews of departmental documents as necessary; Support other departments on ad hoc projects; and.
Clinical Laboratory Data Coordinator Medpace, Inc.Clinical Laboratory Data CoordinatorCincinnati, OhioResponsibilities: Maintain daily routine maintenance over assigned studies via edits, data queries, data changes, and Data Management sample management; Manage and resolve processing errors and inconsistencies daily to ensure client commitment is met (i.e., problem samples, missing samples, misrouted samples, sample testing); Ensure continuous maintenance/follow-up over study assignments to prepare for study timelines (i.e., data locks, study close-out, etc.); Communicate with other internal functional groups and external clients (i.e., sites, vendors, sponsors) on study progress; and. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.