Statistical and Psychology Research Professional* (26.13) SierTeK Ltd.Statistical and Psychology Research Professional* (26.13)Beavercreek, OHFull timePLEASE APPLY DIRECTLY ON OUR WEBSITE www.siertek.com/careersEssential Job Functions• Assist in the development and execution of comprehensive study protocols, including hypothesis formulation, methodology design, data collection strategies, and statistical analysis plans, in coordination with USAFSAM/FESP professional staff. • Coordinate, facilitate, and participate in research team meetings, including leading a recurring weekly meeting to ensure effective communication and progress toward research goals.
Remote Market Research Participant Up to $90/Session No Experience Required Occupons QuebecRemote Market Research Participant Up to $90/Session No Experience RequiredCincinnati, OHIORemoteYou will complete a short screening form so our system can match you with relevant consumer research opportunities within our national insights program. All tasks are conducted online and can be completed outside traditional business hours.
Operations Research Technical Reviewer* (26.49) SierTeK Ltd.Operations Research Technical Reviewer* (26.49)Beavercreek, OHPart timeExperience working with:Air Force medical records systemsDefense Health Agency (DHA) dataApplication Virtualization Hosting Environment (AVHE)Military personnel datasetsExperience supporting:USAFSAM research programsAccession waiver analysisReadiness studiesForce health protection initiativesExperience publishing peer-reviewed scientific manuscripts. Essential Job FunctionsStatistical Analysis & Operations ResearchProvide subject matter expertise in statistical analysis evaluating the long-term impacts of accession medical conditions on:Duty performanceRetentionReadinessForce health outcomesConduct advanced statistical analyses of healthcare and military datasets.
OPERATIONS RESEARCH ANALYST JYG InnovationsOPERATIONS RESEARCH ANALYSTFairborn, OHFull timePossess the ability to design, formulate, conduct, and lead data analysis of operational studies on health surveillance data/health records/other relevant military records and risk reduction of negative health outcomes, readiness, or duty restrictions affecting the USAF total force population Ability to develop, monitor, review, edit, and deliver all products to include technical reports, white papers, publications, memorandums, presentations, and other products. Note: Legitimate correspondence for these positions will only come from @jyginnovations.com or from iSolvedAbout JYG InnovationsJYG Innovations (JYG) is a professional solutions and services company focused on providing innovative and exceptional service in the United States Federal government space, the Department of Defense, State/Local and Commercial sectors.
Research Associate - I Integrated Resources, IncResearch Associate - ICincinnati, OhioContractorKEY SKILL / KNOWLEDGE REQUIREMENTS: Knowledge of anatomy and physiology, Ability to work efficiently as a team member, Excellent communication skills – written/oral/listening, Working with limited supervision, as well as comfort with closer guidance, Independent decision making skills as appropriate, Ability to clearly document and communicate plans and results. EDUCATION / DEGREE / JOB EXPERIENCED REQUIRED: BS or BA preferred, Associate Degree required, preferably in Veterinary Technology, Knowledge of surgical and anesthesia principles, 2 years of veterinary technical experience required (anesthesia experience & surgical support).
Research Associate-I Integrated Resources, IncResearch Associate-ICincinnati, OhioContractorKnowledge of anatomy and physiology, Ability to work efficiently as a team member, Excellent communication skills – written/oral/listening, Working with limited supervision, as well as comfort with closer guidance, Independent decision making skills as appropriate, Ability to clearly document and communicate plans and results. BS or BA preferred, Associate Degree required, preferably in Veterinary Technology, Knowledge of surgical and anesthesia principles, 2 years of veterinary technical experience required (anesthesia experience & surgical support).
Research Associate Integrated Resources, IncResearch AssociateCincinnati, OhioContractorEDUCATION / DEGREE / JOB EXPERIENCE REQUIRED: BS required, MS preferred, with 2 or more years of industrial research, academic research or product development experience desired. A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Medical Imaging Analyst Medpace, Inc.Medical Imaging AnalystCincinnati, OhioResponsibilities: Perform quality assurance checks on medical imaging data collected during medical and device clinical trials to ensure protocol specific requirements are met; Perform established image processing techniques (converting imaging formats, contouring, performing preliminary measurements of lesions and volumes) across multiple modalities (including but not limited to MRI, CT, US, ECHO, DXA, etc.) using proprietary software as well as other third party software; Assist in developing imaging protocols to obtain required study metrics based on clinical trial protocols; Write (in English) technical documents related to the study required imaging procedure. 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.
Medical Director Medpace, Inc.Medical DirectorCincinnati, OhioRemoteResponsibilities: Provide medical management and expertise for clinical trials; Contribute medical expertise to study reports, regulatory documents, and manuscripts; Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials; Participate in new business development through involvement in proposal and sponsor meetings as requested; Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents; Follow specific research related protocol and lead others in strict adherence to the policies. 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.
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.
Experienced Clinical Trials Proposal Writer Medpace, Inc.Experienced 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 financewhile developing your career.
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.
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.
Clinical Supply Chain Project Specialist (Entry) Medpace, Inc.Clinical Supply Chain Project Specialist (Entry)Cincinnati, OhioPreferred majors: Life Sciences, Supply Chain Management, Operations Management, Business, Math; Minimum 1-year industry experience is preferred; Ability to escalate; Prioritization of daily, weekly, monthly, and project workloads; Strong communication and problem-solving skills; Ability to provide excellent internal and external customer support; Must be flexible and able to work in a risk-based environment and understand multiple potential solutions; Solid working knowledge of Power Point, Excel, Word; and. Responsibilities: As a member of Clinical Packaging and Supplies (CP&S) department you will: Support and collaborate in all activities related to investigational product supply chain, potentially including manufacturing, packaging, labeling, storage, and distribution; Monitor alignment of CP&S timelines with project timelines; Attend teleconfrences with internal Medpace teams, Sponsors, and/or Vendors and communicate/present both virtual and face to face; and.
NewAssociate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm Medpace, Inc.Associate Clinical Trial Manager - PhD - Oncology, Hematology, RadiopharmCincinnati, OhioResponsibilities: Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager; Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports within the clinical trial management system; Interact with the internal project team, Sponsor, study sites, and third-party vendors; Provide oversight and quality control of our internal regulatory filing system; Provide oversight and management of study supplies; Create and maintain project timelines; and. Job Summary: Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Oncology, Hematology, and Radiopharm for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team.
Associate Clinical Trial Manager - PhD - Cardiovascular - Cincinnati Medpace, Inc.Associate Clinical Trial Manager - PhD - Cardiovascular - CincinnatiCincinnati, 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. Job Summary: Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Researchers with Cardiology experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) position in our Cincinnati, OH office.
Associate Clinical Trial Manager - PhD - Gastrointestinal (GI) - Cincinnati Medpace, Inc.Associate Clinical Trial Manager - PhD - Gastrointestinal (GI) - CincinnatiCincinnati, 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. Job Summary: Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Researchers with Gastrointestinal (GI) experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) position in our Cincinnati, OH office.
NewAssociate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - Cincinnati Medpace, Inc.Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - CincinnatiCincinnati, 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. Job Summary: Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Ophthalmology for a full-time, office-based Associate Clinical Trial Manager (aCTM) position in our Cincinnati, OH office.
Director, Clinical Trial Management - Neuroscience Medpace, Inc.Director, Clinical Trial Management - NeuroscienceCincinnati, 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. Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add senior-level Directors and established Project Managers to join our Clinical Trial Management Group in Cincinnati, OH.
Associate Clinical Trial Manager - PhD - Postdoctoral - Infectious Diseases - Cincinnati Medpace, Inc.Associate Clinical Trial Manager - PhD - Postdoctoral - Infectious Diseases - CincinnatiCincinnati, 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. Job Summary: Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Infectious Disease areas for a full-time, office-based Associate Clinical Trial Manager (aCTM) position in our Cincinnati, OH office.