135 Results for

Research Associate Jobs in Ohio

Jobs

New!

Columbus, OH5 days ago

$130,000–$170,000 Per Year

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. Excellent academic credentials; Exceptional legal writing and communication skills; Strong interpersonal skills; Strong work ethic and a sense of ownership over work; Ability to manage and prioritize multiple projects.

New!

Cincinnati, OHToday

$140,000–$170,000

Determining compensation for this role (and others) at Vaco by Highspring depends upon a wide array of factors including but not limited to: the individual’s skill sets, experience and training; licensure and certification requirements; office location and other geographic considerations; other business and organizational needs. With that said, as required by local law, Vaco by Highspring believes that the following salary range referenced above reasonably estimates the base compensation for an individual hired into this position in geographies that require salary range disclosure.

Toledo, OH7 days ago

The University is dedicated to the goal of building a culturally diverse and pluralistic faculty and staff committed to teaching and working in a multicultural environment and strongly encourages applications from women, minorities, individuals with disabilities, dual-career professionals and covered veterans. With the exception of positions within University of Toledo Main Campus and the University of Toledo College of Medicine and Life Sciences, the employment offer is conditional upon successful completion of a cotinine test and Occupational Health clearance.

Beachwood, OH10 days ago

The Staff Data Scientist will typically work on 3-5 large projects concurrently that have organization-wide impact.???In addition to these projects, the Staff Data Scientist will provide technical consultation, advice and training on all major on-going Data Science and Analytics projects. Willingness to travel as necessary, work the required schedule, work at the specific location required, complete Penske employment application, submit to a background investigation (to include past employment, education, and criminal history) and drug screening are required.

Cincinnati, Ohio30+ days ago

Remote

SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Responsibilities : Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per.

Cleveland, OH30+ days ago

Full-time

As a full-time employee, you will work on one of our Teams, covering publicly traded companies in one of the following sectors: Consumer, Technology, FinTech, Health Care, or Industrial. Well-developed analytical skills with the ability to master complex tasks and multi-task with minimal supervision.

Cincinnati, Ohio30+ days ago

Responsibilities : Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Qualifications : Must have a minimum of a Bachelor’s degree in a health or science related field; Advanced degrees or prior clinical research experience is a plus; In-House CRA position available for those with no or minimal clinical research experience with rapid advancement; Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits required; Must maintain a valid driver’s license and the ability to drive to monitoring sites; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.

Cleveland, OH30+ days ago

Full-time

As a full-time employee, you will work with our sales team helping to develop relationships with clients and prospects, as well as helping our clients to identify trends in the names that we cover. Work in a team-oriented environment helping to strengthen existing client relationships by driving greater client interactions & usage of CRC channel research product.

Cincinnati, Ohio30+ days ago

Remote

Responsibilities : Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Qualifications : Clinical Research Associate Experience (minimum 1 year); Ability to travel 60-70% to locations nationwide is required; Must have a minimum of a bachelor’s degree in a health or science related field; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.

Mason, OH30+ days ago

$20–$26.50 Per Hour
Contractor

We are seeking a Senior Research Associate – R&D to support our client’s hands-on experimentation and applied research in a fast-paced R&D environment. Trust we genuinely want the best for you and trust we want to move your career forward.

Cincinnati, Ohio30+ days ago

Candidates must have at minimum a Bachelor’s degree in a health or science related field, minimum one year of clinical research experience or relevant direct industry experience (e.g., CRC), ability to travel nationwide, must be detail-oriented, strong time management, and communication skills. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.

MASON, OH30+ days ago

How to originate/revise Specification in Enovia, including BOM table, performance table and attribute data, using Enovia front end. *** expects the contractor to execute the changes and the contractor to be experienced in: How to update user form to be able to originate Hair Care Specifications.

Cleveland, OH30+ days ago

In this role, you will have an opportunity to: Your Key Responsibilities: • Operate and even develop benchtop test equipment for characterizing a variety of material properties and conducting reliability testing. Qualifications: **Bachelor's or associate degree in electrical/mechanical or relevant engineering Responsibilities: Engineering Associate – suitable for individuals with strong interest and background in science and engineering.

Cincinnati, Ohio30+ days ago

Responsibilities : Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Qualifications : Must have a minimum of a Bachelor’s degree in a health or life science related field; Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits required; Must maintain a valid driver’s license and the ability to drive to monitoring sites; Minimum 1 year healthcare-related work experience preferred; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.

Columbus, OH30+ days ago

Full-time

Your work will directly impact the design, architecture, and functionality of our offerings, collaborating with cross-functional teams to contribute to discussions on design and research, and leading the decision on which methods best suit key design questions. Demonstrated experience in collaborating with cross-functional teams, including UX designers, product managers, and developers, to propel customer-centric decision-making and inform product prioritization .

Cincinnati, Ohio30+ days ago

Responsibilities : Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Qualifications : Must have a minimum of a Bachelor’s degree in a health or science related field; degree in Physical Therapy or Kinesiology preferred; Ability to travel 60-70% to locations nationwide is required; Must maintain a valid driver’s license and the ability to drive to monitoring sites; Minimum 1 year healthcare-related work experience preferred; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.

Cleveland, OH30+ days ago

Three years of experience working as a clinical research coordinator working with human subjects, or two years of experience and one of the following certifications: • Certified Clinical Research Coordinator (CCRC) by the Association of Clinical Research Professionals (ACRP) • Certified Clinical Research Professional by the Society of Clinical Research Associates (SOCRA). Currently a Certified Clinical Research Coordinator (CCRC) by the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SOCRA).

New!

Cleveland, OH3 days ago

Cincinnati, OH30+ days ago

Full-time

Ensure consistency and effective communication during study visits and assure all procedures are conducted in compliance with the clinical protocol; Maintain subject safety, assess feedback from study participant and refer to investigators or other professionals as needed; If applicable, administer study medications based on state licensure, account for medications used . Create source templates for study documentation, complete case report forms, and other study specific documents seeking assistance from Senior Clinical Research Coordinator, Principal Clinical Research Coordinator, Team Leader or Clinical Site Director, as needed .

Cincinnati, OH30+ days ago

Full-time

Ensure consistency and effective communication during study visits; Assure all procedures are conducted in compliance with the clinical protocol; Maintain subject safety, assess feedback from study participant and refer to investigators or other professionals as needed; If applicable, administer study medications based on state licensure, account for medications used. Conduct clinical research in compliance with all applicable regulations; Request assistance and technical advice from Senior Clinical Research Coordinator, Principal Clinical Research Coordinator, Team Leader or Clinical Site Director, as needed.

Cincinnati, OH30+ days ago

Completes study documentation and maintains study files in accordance with sponsor requirements and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms. Assists the Principal Investigator and Regulatory Specialist in submission of accurate and timely closeout documents to applicable federal agencies, and the sponsoring agency in accordance with federal regulations and sponsoring agency policies and procedures.

Cleveland, OH30+ days ago

We are seeking established Clinician Scientists with advanced training in Cerebrovascular Diseases, Stroke, or Neurocritical Care, and a passion for leading, mentoring, and grow externally funded investigator-initiated research, clinical trials, and health services research program of the Center. The Cerebrovascular Center is a multidisciplinary clinical, educational, and research department composed of the sections of stroke and vascular neurology, neurocritical care, cerebrovascular neurosurgery and endovascular surgical neuroradiology services within the Neurological Institute.

Cincinnati, OH30+ days ago

Assures all regulatory packets are complete and any required follow-up or adjustments are performed in a timely manner, allowing department to maintain its position of first initiated or early entry site; independently communicates with the sponsors to define tasks and assure efficiency in completion, representing Lindner Research-Oncology in a professional manner. To support the regulatory team in maintaining superior performance in assuring all regulatory tasks and documents are accurate, complete, and properly processed to external and internal contacts; Promotes quality and efficiency in the regulatory process of Lindner Research-Oncology achieving accuracy and completing tasks quickly to facilitate early start-up.

Cincinnati, OH26 days ago

REQUIRED SKILLS AND KNOWLEDGE: Photocopier, fax equipment, all medical equipment appropriate to research, ability to make independent decisions, and strong organizational skills with good follow through practices, excellent communication skills, excellent clerical skills and functional computer knowledge and medical terminology required. 3. Creates and organizes professional presentations for Medical Director and other associates of The Center. • Provides for professional presentations via PowerPoint or other educational media.

New!

Granville, OH3 days ago

Full-time

Working in a structured Stage-Gate innovation environment, this role will support innovation project from early-stage concepts to industrialization and commercialization partnering across R&D, manufacturing, sourcing, quality and marketing to deliver high-performance composite solutions used across wind energy, automotive, construction, and infrastructure. The Research Scientist - Composites Chemistry & Product Innovation is a hands-on R&D role focused on supporting the synthesis and optimization of fiber sizing and coating chemistries compatible with thermoset and thermoplastic resin systems through fiberizing, prototyping, and testing.

Cleveland, OH12 days ago

Train with existing contract technicians in areas such as: ION Thruster hardware integration of Space Power related components into test chambers; Safe operation of test facility systems leading to the status of a qualified operator; Perform facility maintenance, troubleshooting, test buildup, and repairs as needed. The Test Facilities Operation, Maintenance and Engineering (TFOME) contract at the NASA Glenn Research Center provides engineering and technical services in the aeronautics, space power and propulsion test facilities.

Cleveland, OH8 days ago

The position involves engagement with NIH-funded projects, clinical and investigator-initiated trials focused on sleep disorders and their comorbidities, as well as translational work targeting conditions such as obstructive sleep apnea, insomnia, hypersomnia, and circadian rhythm disturbances. Located at the heart of Cleveland, the Clinic's main campus offers a vibrant environment with rich clinical, research, and community engagement opportunitiesmaking it an ideal setting for pioneering sleep disorder research and clinical excellence.

Cincinnati, Ohio30+ days ago

Qualifications : BSN is required; 3+ years of Clinical Nurse experience required, research nurse experience preferred; Experience in Phases 1-4; Phases 2-3 preferred; Management of overall project timeline; Strong leadership skills. Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers with established Clinical Research Nursing backgrounds to join our Clinical Trial Management Group.

Cincinnati, Ohio30+ days ago

Manage electronic filing system for trial documentation; Track, maintain, and perform quality check of electronic documents; Communicate with internal associates globally regarding errors in trial documents; and. In this position, you will be working with a highly experienced team of other administrators and clinical research professionals that can help you grow your skillset while working for a growing and developing company.

Cincinnati, Ohio30+ days ago

Responsibilities : Engage in clinical trial management on a day to day level; Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports; Interact with the Sponsor, study sites, and internal associates; Provide oversight and quality control of our internal regulatory filing system; Manage study supplies; Create and maintain project timelines; and. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.

Cincinnati, Ohio26 days ago

Cincinnati, Ohio30+ days ago

Responsibilities : Engage in clinical trial management on a day to day level; Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports; Interact with the Sponsor, study sites, and internal associates; Provide oversight and quality control of our internal regulatory filing system; Manage study supplies; Create and maintain project timelines; and. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.

Cincinnati, Ohio30+ days ago

Columbus, OH15 days ago

Full-time

Responsibilities As an Administrative Assistant for the State of Ohio Office of Properties & Facilities, you will support both high-level reporting and day-to-day logistics. Candidates who receive an offer will be required to successfully complete a background check and drug test as a condition of employment.

Worthington, OH25 days ago

$115,000–$115,000 Per Year

This is a partner-track position for an attorney ready to take ownership of cases, appear in court, and make an immediate impact handling complex real estate, consumer protection, and business litigation matters. Draft, edit, and finalize legal documents including but not limited to pleadings, dispositive motions, discovery responses and disputes, trial briefs, and post-trial motions.

Columbus, OH17 days ago

Remote

$55,000–$70,000 Per Year
Full-time

Please note: If this position is posted as either fully remote and/or hybrid, in accordance with company policy, individuals residing within a 50-mile radius of a branch location may be required to work onsite in a hybrid capacity as there may be occasions when on-site presence is necessary to meet specific business needs. Renewal Process: Conduct client research, gather underwriting information, perform loss run analysis, prepare submissions, evaluate and negotiate coverages and pricing, prepare and present proposals, bind coverage, and follow up for policy issuance.

Akron, OH17 days ago

Remote

$23–$27 Per Hour
Full-time

Task Processing: Handle policy endorsements, audits, cancellations, reinstatements, lost policy releases, check requests, invoices, finance agreements, summaries of insurance, loss runs, MVRs, ID cards, certificates, binders, billing inaccuracies, and Agent of Record letters. New and Renewal Business Support: Conduct client research, gather underwriting information, perform loss run analysis, prepare submissions, evaluate and negotiate coverages and pricing, prepare and present proposals, bind coverage, and follow up for policy issuance.

Columbus, OH18 days ago

Remote

$55,000–$75,000 Per Year
Full-time

Cincinnati, OH30+ days ago

Remote

Full-time

Albany, New York, United States of America, Annapolis, Maryland, United States, Boston, Massachusetts, United States of America, Burlington, Vermont, United States, Charleston, West Virginia, United States, Cincinnati, Ohio, United States of America, Concord, New Hampshire, United States, Dover, Delaware, United States, Harrisburg, Pennsylvania, United States, Hartford, Connecticut, United States, Lansing, Michigan, United States, Providence, Rhode Island, United States of America, Richmond, Virginia, United States of America, Trenton, New Jersey, United States of America, Washington, District of Columbia, United States of America. Lead and/or support priority market access initiatives/capabilities, as assigned, such as, but not limited to, local market access initiatives, integrated payer-provider relations strategies, reimbursement/market access assessments, reimbursement hotline management, evidence dissemination workstreams, internal/external training, etc.).Support innovative/value-based contracting initiatives including, but not limited to customer engagement, dissemination of evidence and coordination of other HEMA functions.

Dublin, OH30+ days ago

$130,000–$150,000
Full-time

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. The ideal candidate will be a problem solver, an excellent communicator, and a team player, with a passion for justice and a proven track record in the legal field.

Westerville, OH30+ days ago

$90,000–$110,000
Full-time

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. The ideal candidate will be responsible for handling a wide range of legal matters, including Commercial Litigation, Construction, Real Estate, Business Law, and Estate Planning.

Cleveland, OH30+ days ago

Full-time

Assist Research Leadership Team in gathering and analyzing materials for quarterly employee reviews, along with additional strategic initiatives across the firm. If you are interested in equity and market research within an environment that fosters teamwork and excellence, Cleveland Research could be the place for you!

Columbus, OH30+ days ago

Serve as a technical contributor during technology transfer activities from Process Development or clients into GMP Manufacturing, including defining critical quality attributes, key process parameters, and conditions essential for compliant manufacturing under cGMPs. This multidisciplinary role collaborates closely with process development, manufacturing, quality, validation, facilities and engineering, and regulatory teams to ensure upstream, downstream, fill‑finish, buffer preparation, and support‑function processes are scalable, robust, and aligned with regulatory expectations.

Cleveland, OH30+ days ago

Works collaboratively with senior leadership to support the risk management program by leading a proactive approach to mitigating clinical risk, including leading the development of comprehensive strategies to identify and mitigate clinical risks, monitoring and guiding the progress of current risk strategies and strategic action plans, and supporting the efficient and effective management of pending clinical and professional claims in clinical operations, including emergency medicine, pediatrics, pharmacy, behavioral health, OB-GYN, physical medicine and rehabilitation, primary care, surgery, radiology correctional medicine, telemedicine, patient experience, campus security, and other assigned areas. Strong knowledge of legal theory and practice, and knowledge of specific laws and regulations imposed on health care systems by various agencies.

New!

Cleveland, OH1 day ago

Allogen is an American Society for Histocompatibility and Immunogenetics (ASHI) accredited laboratory that provides histocompatibility testing and clinical consulting for bone marrow (BMT) and solid organ transplant (SOT) programs, supporting approximately 1000 transplants annually and donor typing for a local Organ Procurement Organization (OPO). Section of Histocompatability/Division of laboratory Medicine/Robert J. Tomsich Department of Pathology and Laboratory Medicine/Diagnostics Institute of Cleveland Clinic is looking for an assistant/associate director to support the histocompatibility clinical services of Allogen laboratories.

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Research Associate Jobs in Ohio

Directors and Officers Liability Associate Jobot

Litigation Associate Vaco LLC

Assistant, Associate, or Full Professor - Department of Pathology, Surgical Pathologist The University of Toledo

Staff Data Scientist Penske Truck Leasing Co., L.P.

Clinical Research Associate - Clinical Research Coordinator Experience Medpace, Inc.

Equity Research Associate- Entry Level Cleveland Research Company

Clinical Research Associate - Cincinnati, OH (Entry-Level) Medpace, Inc.

Equity Research Sales Associate (Hedge Fund Sales) Cleveland Research Company

Home-Based Experienced CRA (Clinical Research Associate)- Bonus/Equity Medpace, Inc.

Senior Research Associate Gus Perdikakis Associates Inc

Experienced Clinical Research Associate - Hematology/Oncology Medpace, Inc.

Senior Research Associate Lancesoft

Technical Associate - Research & Development TechDigital

Clinical Research Associate (PhD Candidates) Medpace, Inc.

Experience Research Senior Associate JPMorgan Chase Bank, N.A.

Clinical Research Associate (Physical Therapist Candidates) Medpace, Inc.

Coordinator Clinical Research II-Clinical Research Staff MetroHealth

Coordinator Clinical Research II- Research Infectious Disease MetroHealth

Clinical Research Coordinator (level dependent on experience) CTI Clinical Trial Services, Inc.

Clinical Research Nurse Coordinator CTI Clinical Trial Services, Inc.

Clinical Research Coordinator Gastro Health

Director of Cerebrovascular Research Cleveland Clinic Foundation

Regulatory Assistant - MOB Linder Research HV - Full Time - Days The Christ Hospital Health Network

Executive Assistant - MOB Lindner Department Research HV - Full Time - Days The Christ Hospital Health Network

Research Scientist Original Composites and Fibers

Journeyman Research Laboratory Mechanic (RLM) Technician - Vacuum Facilities Sierra Lobo, Inc.

Director of Research- Sleep Disorder Center Cleveland Clinic Foundation

Clinical Trial Project Manager - Research Nurses Medpace, Inc.

Clinical Research Documentation Administrator (TMF) Medpace, Inc.

Clinical Research Project Coordinator - Cardiovascular, Renal, Metabolic Medpace, Inc.

Clinical Research Project Coordinator - Oncology Medpace, Inc.

Entry-Level Research Project Coordinator Medpace, Inc.

Clinical Research Project Coordinator - Neuroscience Medpace, Inc.

Cincinnati Clinical Research Project Coordinator Medpace, Inc.

Clinical Research Project Coordinator - Immunology Medpace, Inc.

Clinical Research Project Coordinator - Infectious Disease Medpace, Inc.

Clinical Research Project Coordinator - Gastrointestinal/GI Medpace, Inc.

Clinical Research Project Coordinator - Ophthalmology Medpace, Inc.

Admin Services Associate Metasys Technologies, Inc.

Senior Associate Attorney Kohl & Cook Law Firm LLC

Account Manager Associate- Commercial Insurance Insurance Office of America

Senior Account Associate - Commercial Lines/Select Business Unit (SBU) Insurance Office of America

Senior Account Associate- Commercial Insurance Insurance Office of America

Associate Director, HEMA Provider Relations – MedTech Surgery Johnson and Johnson

Litigation Associate Jobot

Associate Attorney Jobot

People Operations Associate Cleveland Research Company

Senior Associate Scientist, MS&T Downstream Forge Biologics

Sr Associate General Counsel- Litigation & Clinical Risk MetroHealth

Laboratory Assistant/Associate Director - Allogen Laboratories Cleveland Clinic Foundation

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