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Clinical research associate Jobs in Toledo, OH
Clinical Research Coordinator II - MOB Lindner Research HV - Full Time - Days
The Christ HospitalOhio, USAssociate Manager Clinical Health Services (OhioRISE)-3
CVS HealthWork from hom, OH, US- Promoted
- New!
CLINICAL COUNSELORS
Third Street Family Health ServicesOH, United States- Promoted
- New!
CLINICAL PHARMACIST
Cleveland ClinicOH, United States- Promoted
Research Participants - Part Time
AFGToledo, OH, United StatesSenior Clinical Research Associate - Oncology - Northeast
Worldwide Clinical TrialsOhio, USARN Clinical Research Coordinator - Neuro Research
ProMedicaToledo, OH, US- Promoted
- New!
Clinical Psychologist
Behavioral Care SolutionsToledo, OH, US- Promoted
- New!
CLINICAL COORDINATOR
Harbor, Inc.OH, United States- Promoted
Research Assistant (Remote)
D Aceto Services LLCToledo, Ohio- Promoted
Clinical Therapist
HarborToledo, OH, United States- Promoted
Clinical Psychologist
SimplyApplyToledo, OH, United States- Promoted
CLINICAL SUPERVISOR
FCS, IncOH, United States- Promoted
Clinical Research Associate
VirtualVocationsToledo, Ohio, United States- Promoted
Clinical Psychologist
United States Air ForceRossford, OH, United StatesClinical Research Associate - Oncology - Ohio
PRA Health SciencesOH, USAssociate Clinical Research Monitor, Midwest
Edwards LifesciencesUSA, Ohio, Remote- Promoted
Clinical Therapist
ZepfNorthwood, OH, United StatesResearch Analyst
WelocalizeOhio- Promoted
CLINICAL DIETITIAN
Healthcare Services Group, Inc.OH, United StatesClinical Research Coordinator II - MOB Lindner Research HV - Full Time - Days
The Christ HospitalOhio, US- Full-time
Job Description
Specialized research professional working with and under the direction of the Principal Investigator (PI) and the Lindner Center for Research and Education. While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. The CRC ensures quality, human subject safety and data integrity of the clinical trial. By performing these duties, the CRC works with the PI, department, sponsor, Lindner Center and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.
Responsibilities
Study Conduct / Clinical Research Practice
- Maintain awareness of status of all active studies.
- Arrange for facilities and supplies.
- Ensure participant and study compliance, i.e. collection of specimens or data.
- Collaborate with investigator(s) and coworkers to ensure proper progress and completion of clinical studies.
- Register, schedule, and conduct clinical study visit in conjunction with other(s), such as PI, and / or other clinical services.
Regulatory Compliance and Documentation
Recruitment, Enrollment, and Retention
Data Management
Assist in data analysis and maintain record keeping and data storage
Communication
Qualifications
KNOWLEDGE AND SKILLS :
Please describe any specialized knowledge or skills, which are REQUIRED to perform the position duties. Do not personalize the job description, credentials, or knowledge and skills based on the current associate. List any special education required for this position.
EDUCATION : Bachelor’s degree required; Masters preferred
YEARS OF EXPERIENCE : 2-4 years clinical research experience with conducting clinical trials / studies
REQUIRED SKILLS AND KNOWLEDGE : Photocopier, fax equipment, software and database skills, all medical equipment appropriate to research and strong organizational and communication skills.
LICENSES & CERTIFICATIONS :
Preferred clinical research certifications, such as CCRA or other applicable research certifications