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Jobs

Senior Director - Clinical Research _ Office of Associate Vice Chancellor for Research University of Mississippi Medical Center

Senior Director - Clinical Research _ Office of Associate Vice Chancellor for Research
Jackson, MS

Collaborates with internal and external key collaborators including departments, leaders across the organization, representatives from external agencies/organizations to provide mentorship, resolve issues, grow clinical trials, and/or implement processes and/or solutions. Education and Experience Required: Bachelor's degree and seven (7) years of work experience in clinical research operations, regulatory compliance, or clinical trials management, including two (2) years of experience in a supervisory role.

30+ days ago
New

Research Support Specialist Mass General Brigham

Research Support Specialist
Somerville, Massachusetts

The Center provides a range of clinical services to women, which include: consultation regarding the use of psychiatric medications during pregnancy; treatment for postpartum mood and anxiety disorders; treatment for premenstrual syndrome; and treatment of menopause-related mood and anxiety symptoms, sleep disorders, and hot flashes. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success.

3 days ago

Senior Clinical Research Coordinator - Psychiatry Washington University in St Louis

Senior Clinical Research Coordinator - Psychiatry
St. Louis, MO
  • $64,300–$99,700 / year

Provides study coordinator functions and performs all duties associated with the coordination and implementation of clinical research study/projects, data collection, and the management of data generated by study protocols; consents participants for non-therapeutic clinical trials and performs blood draws and other specimen collection as needed. Skills: Clinical Research Management, Clinical Study Protocols, Computer Systems, Database Management, Data Entry, Detail-Oriented, Freezerworks (Software), Interpersonal Communication, Microsoft Office, Ordering Supplies, Organizing, Participant Recruiting, Research Projects, Research Support, Written Communication.

21 days ago
University of Utah logo

Assistant or Associate Professor (Clinical)- Spine Neurosurgery University of Utah

Assistant or Associate Professor (Clinical)- Spine Neurosurgery
Salt Lake City, UT

The University of Utah values candidates who have experience working in settings with students, staff, faculty and patients from all backgrounds and possess a strong commitment to improving access to higher education, employment opportunities, and quality healthcare for historically underrepresented groups. The candidate will be committed to working within an active academic department with clinical, teaching and research responsibilities and/or developing a community-based practice across a broader spine-based spectrum of services.

30+ days ago
NYU Langone Medical Center logo

Research Coordinator - Neuro - Patchogue NYU Langone Medical Center

Research Coordinator - Neuro - Patchogue
Patchogue, NY
  • $58,500–$67,567.50 / year

Human Subjects' Research - As applicable, oversee the submission of necessary documents required by the NYU Institutional Board (IRB), NYU Office of Clinical Trials and any other appropriate parties in order to obtain approval to conduct human subjects research (e.g., ensures the update and submission of necessary documents and/or forms to appropriate destination). In this role, the successful candidate will be responsible for providing moderate to advanced range of coordination of Research studies conducted at the Medical Center, assists with the recruitment, enrollment, grant submissions, research data collection and study coordination activities.

30+ days ago

Clinical Research Associate-Regulatory Eisenhower Health

Clinical Research Associate-Regulatory

Good Clinical Practice (GCP) Course and Human Subjects Research (HSR) course within thirty (30) days of hire Preferred: Master’s degree Licensure/Certification: Preferred: ACRP CCRC or SOCRA CCRP Certification; certification required upon eligibility Experience: Required: Two (2) years of experience with clinical trials or related regulatory experience Preferred: Experience working with FDA regulations, NCI policies and procedures, and Good Clinical Practice guidelines for the conduct of clinical research; experience developing and maintaining record management systems; experience preparing various forms, documents and reports Reports To: Director-Research Administration Supervises: N/A Ages of Patients: Adult, Geriatric Blood Borne Pathogens: Minimal/ No Potential. Ability to analyze issues, identify root causes, and develop solutions, Ability to create and maintain positive interpersonal relations with peers, staff, leaders and vendors, Ability to maintain high degree of confidentiality, Ability to organize information or data to facilitate easy retrieval and use, Ability to prioritize tasks and manage time efficiently to meet deadlines, Knowledge of medical and pharmaceutical terminology and concepts, as well as theoretical knowledge, Written and verbal communication skills Essential Responsibilities .

30+ days ago

Clinical Research Associate II Bio-Rad Laboratories Inc

Clinical Research Associate II
Seattle, WA
  • $83,000–$114,200 / year

This role represents Clinical Affairs collaborates cross-functionally with Regulatory Affairs, R&D, Quality, Marketing, and external partners to deliver high-quality clinical data and evidence supporting product registration and commercialization of Bio-Rad diagnostic products. Actual compensation will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors.

20 days ago

Clinical Research Coordinator II University of Pittsburgh

Clinical Research Coordinator II
Pittsburgh, PA

Based Upon Qualifications'',''TBD Based Upon Qualifications'',''No'',''No'',''No'',''No'',''For position finalists, employment with the University will require successful completion of a background check'',''For position finalists, employment with the University will require successful completion of a background check'',''Not Applicable'',''Not Applicable'',''Resume, Cover Letter'',''Resume, Cover Letter'',''Not Applicable'',''Not Applicable'',''false'',''449495'',''449495'',''true'',''449495'',''false'',''Submission for the position: Clinical Research Coordinator II - (Job Number: 26004680)'',''false'',''449495'',''false'',''true''. ''449495'',''true'',''449495'',''false'',''Submission for the position: Clinical Research Coordinator II - (Job Number: 26004680)'',''false'',''449495'',''false'',''true'',''Clinical Research Coordinator II'',''Health Sciences Core Research Facilities'',''Pennsylvania-Pittsburgh'',''26004680'',''!*!

14 days ago
New

Equity Research Associate – Immuno-Oncology Leerink Partners

Equity Research Associate – Immuno-Oncology
New York

This individual will work closely with senior equity research professionals on scientific, clinical, commercial, financial, and strategic assessments of companies developing cancer immunotherapies — from cell therapy to traditional modalities, and small/mid-cap to large-cap biopharmaceutical companies. Strong quantitative and analytical skills, including hands-on experience with statistical or simulation-based analysis (e.g., Monte Carlo/revenue simulation, survival analysis); preference for candidates with working knowledge of biostatistics and/or quantitative surveys.

4 days ago

Sr. Manager, Clinical Trial Liaison Kiniksa Pharmaceuticals

Sr. Manager, Clinical Trial Liaison
Philadelphia, New York

This role focuses on building strong relationships with investigative sites, identifying barriers to screening and enrollment, supporting protocol and operational education, ensuring contemporaneous and accurate data entry, and escalating site-level risks that may impact study execution, participant retention, data quality, or documentation readiness. Build and maintain productive relationships with Principal Investigators, study coordinators, research nurses, site managers, and other relevant site personnel, and serve as a sponsor representative and primary site engagement contact for assigned sites.

12 days ago

Clinical Research Associate II/III Novotech Health Holdings Pte Ltd

Clinical Research Associate II/III
NY
  • $70,000–$140,000 / year

Preferably experience of working in the research, pharmaceutical industry or a related field per job level as follows: CRA II: Approximately 1-2 years of Clinical Research Associate experience or equivalent experience (CRA II fast track) in other roles in the Clinical industry. Provide written and verbal site updates (including monitoring visit reports) on study progress to the PM/LCRA according to the study requirements/timelines as documented in the Clinical Monitoring Plan and Sponsor/Novotech SOPs.

30+ days ago
AtriCure logo

Clinical Research Associate II AtriCure

Clinical Research Associate II
Minnetonka, Ohio

The CRA II will also conduct site visits including Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits, and Close Out Visits. The CRA II will be responsible for the study start up process for AtriCure’s Clinical Investigational protocols, which includes and is not limited to the following: protocol review, Informed Consent Development, CRF design, EDC testing, preparation of site-specific logs/documentation and investigator study files.

30+ days ago

Senior Clinical Research Coordinator Iterative Scopes Inc.

Senior Clinical Research Coordinator
Dayton, OH

CRC) at Iterative Health you will serve as a key team member within the clinical research site, overseeing complex studies while supporting staff development, operational performance, and high-quality patient experiences. This role combines hands-on study coordination with mentorship, process improvement, and cross-functional collaboration to help drive successful study execution, enrollment performance, and regulatory compliance.

10 days ago

Clinical Research Coordinator I School of Medicine, Infectious Diseases (Hope Clinic) Emory University

Clinical Research Coordinator I School of Medicine, Infectious Diseases (Hope Clinic)
Decatur, GA

To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). This position is intended to support clinical research and all clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher.

30+ days ago

Clinical Research Coordinator II School of Medicine, Hope Clinic Emory University

Clinical Research Coordinator II School of Medicine, Hope Clinic
Decatur, GA

To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). KEY RESPONSIBILITIES: Manages research project databases, develops flow sheets and other study related documents, and completes source documents/case report forms.

30+ days ago
New

Clinical Research Coordinator II School of Medicine, Human Genetics Emory University

Clinical Research Coordinator II School of Medicine, Human Genetics
Atlanta, GA
Remote

To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). KEY RESPONSIBILITIES: Manages research project databases, develops flow sheets and other study related documents, and completes source documents/case report forms.

6 days ago

Senior Clinical Research Associate Immatics NV

Senior Clinical Research Associate
Houston, TX
Remote
  • $120,000–$135,000 / year

In this role, you will partner closely with clinical sites and cross-functional teams to support high-quality study execution, patient recruitment, and operational excellence across clinical trials. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics.

23 days ago

Clinical Research Coordinator I - The School of Nursing - Alzheimer's Disease Prevention Emory University

Clinical Research Coordinator I - The School of Nursing - Alzheimer's Disease Prevention
Atlanta, Georgia
  • Full time

Discover Your Career at Emory University: Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. Duties include facilitating all aspects of study visits, performing phlebotomy, cognitive testing, vascular ultrasound, wet lab biospecimen processing and adherence to study protocols.

16 days ago

Clinical Research Coordinator III - Pediatrics Hematology & Oncology Washington University in St Louis

Clinical Research Coordinator III - Pediatrics Hematology & Oncology
St. Louis, MO
  • $58,300–$90,400 / year

Primary Duties & Responsibilities: Manages protocol study start up and study launch, submission, and maintenance of essential regulatory documents; assists in budget review and invoice tracking; assists in scheduling and facilitating site visits by external and internal monitors and auditors; provides high level of direct and indirect support. Skills: Analyze Information, Clinical Research Management, Clinical Study Protocols, Database Management, Interpersonal Communication, Leadership, Oral Communications, Prioritization, Problem Solving, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS), Supervision, Written Communication.

7 days ago

Clinical Research Coordinator III (RN) Florida Cancer Specialists and Research Institute

Clinical Research Coordinator III (RN)
Bradenton, FL

We are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida. Our patients have access to ground-breaking therapies, in a community setting, and may participate in national clinical research studies of drugs and treatment protocols.

30+ days ago
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