57 Results for

Medical Science Liaison Jobs in Ohio

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Cincinnati, OH3 days ago

The Department of Psychiatry and Behavioral Neuroscience is dedicated to high quality medical student, resident, and fellow education, excellence in patient care, and advancing the science in psychiatry and behavioral neurosciences through clinical trials and ongoing collaborative research. The department supports clinical care and career development in multiple disciplines, including general psychiatry, addiction psychiatry, forensic psychiatry, consultation-liaison psychiatry, geriatric psychiatry, and neuromodulation including electroconvulsive therapy and transcranial magnetic stimulation.

Cincinnati, OH30+ days ago

$150,000–$200,000 Per Year

Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Job Responsibilities and Duties include, but are not limited to, the following: Systematically identify and develop relationships with healthcare professionals (HCPs) and key opinion leaders (KOLs) to raise awareness of Axsome's mission to accelerate the invention and adoption of life-changing medicines for patients living with CNS disorders.

Cleveland, OH9 days ago

Remote

$85,000–$150,000 Per Year

Our team is growing, and we currently have an immediate opening for a Medical Science Liaison (MSL)Title: Medical Science Liaison (MSL)Location: Remote or Hybrid (Cleveland, Ohio)Reports to: VP Medical Affairs or Chief Medical OfficerJob Description: The Medical Affairs Professional serves as a key scientific and clinical expert for Cleveland Diagnostics flagship IsoPSA product, a Class III In Vitro Diagnostic (IVD) assay for prostate cancer risk stratification. 2. Evidence Generation and Research SupportSupport clinical research initiatives under the supervision of the Clinical Operations team by serving as a primary contact to investigators for investigator-initiated studies (IIS), facilitating internal review of IIS proposals for feasibility and conduct, identifying potential sites/investigators for sponsored trials, and assisting in site communications during active sponsored trials.

Cleveland, OH30+ days ago

Remote

Full-time

Develop and maintain an advanced level of knowledge about pertinent studies, compounds, and diseases that would facilitate collegiate and scientific discussions with leading hematology/oncology thought leaders. Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty pharmaceuticals meeting the high medical needs of rare disease patients and providing treatment and services to them.

Cleveland, Ohio30+ days ago

$152,500–$186,500 Per Year

The MSL will primarily identify and engage with a targeted group of national and regional thought leaders/healthcare professionals (HCPs) as well as payers and managed care accounts, providing the consistent delivery of educational and compliant scientific information in support of Oncology products. Driven by a bold pursuit of science and fueled by an unwavering commitment to patients, Sun Pharma is a leading global pharmaceutical company, providing high-quality medicines trusted by healthcare professionals and patients.

Cleveland, OH30+ days ago

Remote

$180,000–$225,000 Per Year

This Director (or Associate Director) level MSL will own a defined US territory with primary responsibility in sickle cell disease (SCD) and shared accountability across the Beam pipeline, including Alpha‑1 antitrypsin deficiency (Alpha‑1) and glycogen storage disease 1a (GSD). Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.

Cleveland, OH30+ days ago

The Associate Director/Director, MSLs is responsible for the leadership, direction and management of MSLs in the region and works collaboratively with the Medical Affairs Senior management with strategic and tactical planning, working collaboratively with Medical Affairs and Clinical Development teams for support of clinical studies across the product portfolio. Skills:Communication & Cross-functional Influence, Critical Thinking & Agility, Healthcare Environment Dynamics, KOL/ HCP Engagement, Medical Data and Insights, People Development, Resource Planning & Management, Territory Management (MSL).

Cleveland, OH30+ days ago

Full-time

Our Neuroscience team tackles the world's toughest brain health challenges including multiple sclerosis, Alzheimer's disease, Parkinson's disease, myasthenia gravis, epilepsy, major depressive disorder, bipolar disorder, schizophrenia, and autism. This individual will help ensure that products are used effectively as scientific resources and experts and provide input about relevant scientific and clinical data for these external customers and internal business partners.

Cleveland, OH30+ days ago

Remote

Full-time

MSL) is responsible for providing fair balanced, objective, scientific information, and education to opinion leaders (OLs), health care professionals, and to internal partners as required by scientific and business needs. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.

Cleveland, OH30+ days ago

Remote

Full-time

The Medical Science Liaison (MSL) is responsible for providing fair balanced, objective, scientific information, and education to opinion leaders (OLs), health care professionals, and to internal partners as required by scientific and business needs. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.

Cleveland, OH30+ days ago

Remote

$166,090–$201,262 Per Year

The purpose of their interactions is to engage in meaningful scientific exchange that will ensure patients have access to BMS medicines, to ensure their safe and appropriate usethrough peer to peer discussions aligned with medical strategies and needs expressed by external stakeholders, and to facilitate research. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

Cincinnati, OH30+ days ago

Remote

$166,090–$201,262 Per Year

Columbus, OH9 days ago

Must be highly mobile, able to access all areas of the premises; Ability to concentrate and remain focused while handling multiple tasks, responsibilities and projects; Ability to work over eight hours in a work day, and over 40 in a work week as necessary; Ability to read, comprehend and follow written and verbal instructions. As North America’s largest provider of mobility products and services, we deliver personalized solutions from manual and power wheelchairs to medical supplies and other assistive technologies that support health, independence, and everyday participation.

Miamisburg, OH30 days ago

The Liaison serves as a trusted partner to Community Partnerships & Advocacy leadership, supporting disciplined relationship management, issue tracking, and advocacy coordination that advances Kettering Health’s strategic priorities. The Community and Government Relations Liaison supports the execution of Kettering Health’s government relations and advocacy strategy by providing legislative monitoring, executive communication support, and stakeholder engagement coordination at the local and state levels.

Wright-Patterson Air Force Base, OH13 days ago

Network and Computer Systems Administrator provide technical support to government customers, maintain computer systems, printers, VoIP, user account and permissions management, video telecommunications/teleconference system support, ISSO and Cybersecurity Liaison duties, documentation submission (appointment letters, access requests, etc.). Key responsibilities include computer maintenance, system administration, application of security measures, network object management, user support, backup, and recovery activities, monitoring local, USAF, and DoD computer health and status reporting tools, applying remediation measures, documentation, collaboration with IT teams, and capacity planning.

Cincinnati, OH28 days ago

Remote

$185,000–$190,000 Per Year

Guided by our core values of Patients, Science, and Passion, we are applying our innovative TransCon® technology platform to fulfill our mission of developing new therapies that demonstrate best-in-class potential to address unmet medical needs. This highly visible position collaborates with internal stakeholders to ensure patients receive timely access to needed therapies, supporting safe, appropriate treatment initiation, and reinforcing correct product use.

Maumee, Ohio30+ days ago

We have also created an internal culture that provides the resources and technology needed to encourage personal and professional growth opportunities through reimbursement for education; a free in-house resource for hundreds of educational and self-enrichment courses; mentorship program; wellness program; Women’s Organization and ongoing philanthropic opportunities. Previous use and understanding of AutoCAD and Revit design software with the ability to produce preliminary and schematic designs in AutoCAD at a minimum, but Revit is highly desired.

Columbus, OH30+ days ago

$120,000–$165,000 Per Year

Identify, develop, and maintain professional relationships with key opinion leaders (KOL), consultants, investigators, and healthcare professionals (HCPs) in assigned areas of therapeutic interest to ensure communication of current and emerging medical and scientific information, resulting in improvement of optimal patient care and outcomes. The salary range is the range United Therapeutics Corporation in good faith believes is the range of possible compensation for this role at the time of this posting depending on the candidate’s experience, qualifications, geographic location, and other factors permitted by law.

Columbus, OH30+ days ago

$144,300–$189,400 Per Year

The impact that a MSL will have on the organization includes the following: a) as a representative of Eisai, a MSL will communicate key information about Eisai, the company and its hhc mission; b) provide key scientific and clinical information about Eisai’s products/pipeline; serve as a conduit for communication between Eisai Research and the medical community regarding ideas for future research, and c) provide corporate value through demonstrated leadership, teamwork, participation in strategic thinking, and special projects. MSLs will be trained and certified on AD and Eisai’s dementia pipeline data in order to fulfill educational gaps with KOLs/HCPs and gather medical insights to refine medical strategy and continue to close the gap on unmet educational needs for AD HCPs.

Kirtland, OH9 days ago

Design, develop, and maintain interactive dashboards and reporting solutions using business intelligent tools (Power BI) to extract, transform, and integrate data from multiple relational systems, ensuring data accuracy and integrity. Prepare user-friendly data visualizations for use in presentations (PowerPoint), reports (MS Excel and Word) and interactive dashboards (Power BI); summarize data findings for use by decision-makers in written reports.

Cincinnati30+ days ago

Medi-Weightloss is thrilled to invite an exceptional Nurse Practitioner or Physician Assistant to join our dynamic team in a full-time/ Part-Time/ PRN role, serving our Ohio location. We address the unique needs of patients affected by excess weight and obesity, recognizing obesity as a disease that requires a range of medical interventions.

Cincinnati, OH12 days ago

Join us the DataServ/xFact as our next Design Engineer, working with our Sales and Design Engineer Teams to design leading solutions for our customers throughout Ohio. Five years' experience in the design, implementation and/or management of IT systems including networking, wireless, telephony and server systems.

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, Ohio26 days ago

Qualifications : • Bachelor's degree in Information Systems (or a related field) or Life Sciences and 3 years of experience in the clinical research industry or 3 years of experience as a system administration in a health care field; • Good organizational skills, very detail oriented, flexible, and possess good communication skills; • Ability to interact with staff and external users from multiple countries; • Must be able to work concurrently on several projects, each with specific requirements that may differ from project to project; • Competent in installation and troubleshooting of software. Responsibilities : • Act as a liaison between end users and application development teams while maintaining the interests of end users; • Perform Medical Imaging commercial off-the-shelf applications maintenance, testing and validation.

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.

Newark, Ohio30+ days ago

However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. Complete post audit forms indicating adequacy of the tree trimming and tree removal work, and forward the completed forms to the vegetation management program manager or coordinator.

Cuyahoga Falls, Ohio30+ days ago

However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. Minimum Requirements:Two-year or four-year degree in Forestry, Biology, Natural Resources, Environmental Science or related field OR high school diploma/GED plus two years of UVM experience.

Columbus, OH18 days ago

$91,041.60–$107,099.20 Per Year

This position oversees the effective delivery of construction projects ensuring information technology needs, including networking and infrastructure support mechanisms are considered and integrated into construction projects. Bachelor's degree in business administration, information technology, computer science, or related field and six (6) years' experience managing IT related deliverables in partnership and coordination with construction partners.

Cleveland, OH30+ days ago

Team-building skills to be able to interact and communicate collaboratively and effectively with study teams, investigational drug services and other Clinical Research Center cores to implement a new protocol within the timelines requested by the Principal Investigator; Clinical and research nursing skills to create process-driven documents; Writing skills with good spelling and grammar to be able to translate protocol-specific tasks into documents the DCRU nurses and study teams will follow to schedule and conduct study visits. Adds DCRU-specific tasks into DCRU finance budget template to allow finance to create budget for submission to study team/Research Finance Services within specified UHCRC timelines; Creates study specific order sets, source documents, and scheduling request forms.

Cincinnati, Ohio29 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.

Wright-Patterson AFB, OH8 days ago

The Chief Information Security Officer supports the mission of delivering secure, compliant, and fully operational IT infrastructure for new SCIF military construction requirements by providing expert-level guidance across the design, programming, planning, and management of enterprise-level information technology systems. As a Chief Information Security Officer, you will apply deep expertise in DoD and Intelligence Community IT requirements, the Risk Management Framework, and the Authority to Operate process to translate complex operational and mission needs into a cohesive and resilient enterprise architecture.

Westlake, OH30+ days ago

Full-time

In this role, you won’t just manage studies, you’ll help bring life-changing treatments closer to reality while ensuring patients feel supported every step of the way. We’re seeking an experienced Clinical Research Coordinator who thrives in a fast-paced, detail-oriented environment and understands the importance of both precision and compassion.

Dayton, OH22 days ago

Team Leadership: Lead, supervise, train, and mentor technical staff, including auditors and technical managers, to support high-quality audit performance and professional development. Our founding principles of Service, Integrity and Value are not just words in our tagline; these values are aspirational in that they provide guidance to each and every one at EAGLE in our day-to-day approach to our shared profession, to the public and to each other.

Cleveland, OH30+ days ago

Performs all activities related to clinical research studies including but not limited to: screening participants for eligibility and recruitment, obtains informed consent, educates participants regarding study requirements and completes case report forms (CRF). Works with the Principal Investigator to coordinate all aspects of implementation of assigned multiple and/or complex clinical research trials.

Cleveland, OH30+ days ago

Cincinnati, OH30+ days ago

Expected operating model includes the execution of quality and safety improvement within existing clinical and operational leadership structures (COO, CNO, executive committees, service lines, ambulatory operations). Partner with executive and operational leaders (i.e. COO, CNO, service line leaders, Physician Medical and Administrative Directors) to deliver measurable improvements in quality, safety, and clinical outcomes.

Cincinnati, Ohio29 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.

Cincinnati, OH30+ days ago

Full-time

Installs, configures, and tests POS systems (DRB, ICS), networks, payment kiosks, and related hardware/software to ensure operational readiness. Service all IT systems; all POS Hardware/Software, Network infrastructure, Tunnel Controllers, Ground Loops, Cameras, Phones, Wireless, etc.

Cincinnati, Ohio29 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.

Cincinnati, Ohio29 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.

Cleveland, OH30+ days ago

Performs day-to-day activities related to clinical research studies including: recruit and screens participants, obtain informed consent, educate participants regarding study requirements, and complete source documents and case report forms (CRFs). Works in collaboration with the Principal Investigator to coordinate and implement assigned clinical research studies in accordance with Good Clinical Practice (GCP) guidelines.

Cleveland, OH30+ days ago

Lima, OH30+ days ago

$60,000–$90,000 Per Year

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.

Cleveland, OH19 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).

Cleveland, OH19 days ago

The Director of Research will have the support of a dedicated research supervisor, 15 research coordinators, the Centers own biostatistician and clinical trial design expert, and the patient base from 10 Fellowship-trained movement disorders specialists, 3 functional neurosurgeons, 2 neuropsychologists 2 bioethicists, and 7 advanced practice providers. The Movement Disorders and Functional Neurosurgery Section under the Center for Neurological Restoration is one of the largest clinical programs in the country, with unlimited clinical-research potential, residing within a diverse, multidisciplinary academic Neurological Institute.

Cleveland, OH19 days ago

In 2019, amongst the 18 clinical institutes within Cleveland Clinic, our Neurological Institute ranked #1 in Clinical Research Funding ($28.56M, 28% - direct costs) followed by the Heart and Vascular Institute ($18.36M,18% - direct costs). Our team sees more than 20,000 patients annually, performs almost 5,000 procedures, nearly 2,000 infusions and is the leader in virtual visits and delivery of care by Telemedicine.

Loveland, OH30+ days ago

We currently are seeking several quality, self-driven RN's to work in In-Patient Clinical Research Studies at Cincinnati Children's Hospital Medical Center in Cincinnati, OH. We are offering a PRN opportunity on either day and night working on a clinical research study at Cincinnati Children's Hospital Medical Center.

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Medical Science Liaison Jobs in Ohio

Jobs

Inpatient Psychiatrist, Department of Psychiatry and Behavioral NeuroscienceUniversity of Cincinnati

Medical Science Liaison/Senior Medical Science Liaison, Alzheimer's Disease Agitation (Midwest Region)Axsome Therapeutics

Medical Science Liaison (MSL)Cleveland Diagnostics Inc.

Medical Science Liaison - Hematology Rare Disease - Great Lakes RegionSobi

Medical Science Liaison - Cutaneous Oncology - Cleveland, OHLifelancer

Senior Medical Science Liaison/Medical Science Liaison – Cleveland/Detroit RegionBeam Therapeutics

Associate Director/Director, Medical Science Liaison - Oncology, (Central Region)Eisai

Medical Science Liaison - Neuroscience - OhioJohnson and Johnson

Senior Medical Science Liaison-Neuroimmunology-Great LakesJohnson and Johnson

Medical Science Liaison-Neuroimmunology- Great LakesJohnson and Johnson

Medical Science Liaison, Cardiovascular - Milvexian (North OH)Bristol Myers Squibb

Medical Science Liaison, Cardiovascular - Milvexian (South OH, WV)Bristol Myers Squibb

Clinical LiaisonNumotion

Community & Government Relations Liaison - Community OutreachKettering Health

Cyber Security Liaison - 304694Delaware Nation Industries

Patient Access LiaisonTaylor Strategy Partners

Architectural Project Manager - Science, Technology & IndustryColliers Engineering & Design

Clinical Oncology LiaisonUnited Therapeutics

MSL/Sr. MSL, Neurology - Alzheimer's Disease, Southern Ohio- Field basedEisai

Full-time Staff: Institutional Research Data AnalystLakeland Community College

Nurse Practitioner or Physician AssistantMedi-Weightloss

IT Network Design EngineerDataServ Integrations, LLC

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

Clinical Application Administrator – ImagingMedpace, Inc.

Clinical Research Nurse CoordinatorCTI Clinical Trial Services, Inc.

Clinical Research CoordinatorGastro Health

Consulting Utility Forester (FT)ACRT, Inc.

Contract AdministratorACRT, Inc.

Project Manager, IT ConstructionCentral Ohio Transit Authority

Protocol Nurse, Dahms Clinical Research UnitUniversity Hospitals

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

Chief Information Security OfficerDEFTEC Corporation

Clinical Research CoordinatorADF Medical Services Inc.

Director of Technical Services - Food SafetyEAGLE Certification Group

Clinical Research Specialist II, NeurologyUniversity Hospitals

Clinical Research Specialist II, Peds Hematology/Oncology (Hybrid)University Hospitals

VP- Quality and Clinical EffectivenessUC Health

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

IT Field TechWhiteWater Express Car Wash

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

Clinical Research Associate (PhD Candidates)Medpace, Inc.

Clinical Research Nurse Specialist I, BSN (NE).UHC Peds Endo Metabolism-50680University Hospitals

Clinical Research Nurse Specialist I, RN - Infectious DiseaseUniversity Hospitals

Clinical Research Nurse Specialist II, Pulmonary/Critical Care and Sleep MedicineUniversity Hospitals

Clinical Research Nurse Specialist I, Infectious DiseaseUniversity Hospitals

Clinical Research Coordinator IICare Access

Coordinator Clinical Research II-Clinical Research StaffMetroHealth

Director of Clinical Research - Movement Disorders and Functional NeurosurgeryCleveland Clinic Foundation

Director of Clinical Research - Headache & Facial PainCleveland Clinic Foundation

RN Clinical Research Study PRNCommonSpirit Health at Home

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