Top 295 Clinical research Jobs in Ohio

Clinical Research Associate II
AtriCure —Mason, OH
- $85,000 - $105,000 a year
- Remote
- Background check
- Anatomy knowledge
- Microsoft Excel
- Paid parental leave
- Health insurance
Clinical Research Coordinator I
Nationwide Children's Hospital —Columbus, OH
- Weekends as needed
- Hospital
- Word processing
- Bachelor of Science
Clinical Research Coordinator
OhioHealth —Columbus, OH
- Full-time
- Mid-level
- Bachelor's degree
- Travel
Clinical Research Coordinator-Clinical Trials Management Office
The Ohio State University Wexner Medical Center —Columbus, OH
- Weekends as needed
- Background check
- Pass drug screening
- Mid-level
5d
Clinical Research Scientist
Summa Health —Akron, OH
- $45.26 - $67.89 an hour
- Full-time
- Hybrid work
- Acute care
- Hospital
- Customer service
- AD&D insurance
- Disability insurance
Clinical Research Coordinator I - RI Behav Trials Off
Nationwide Children's Hospital —Columbus, OH
- Weekends as needed
- Hospital
- Word processing
- Writing skills
Clinical Research Coordinator - Cincinnati, OH
IQVIA —Cincinnati, OH
- $35 - $42 an hour
- Part-time
- Vital signs
- Office
- Bachelor's degree
Clinical Research Regulatory Specialist II, Seidman Cancer Center (Hybrid)
University Hospitals —Cleveland, OH
- $56,555 - $88,442 a year
- Computer literacy
- Mid-level
- Mentoring
Clinical Research Quality Assurance Specialist, Seidman Cancer Center (Hybrid)
University Hospitals —Cleveland, OH
- $60,528 - $94,661 a year
- 3 years
- Master's degree
- Bachelor's degree
Clinical Research Coordinator
Wright State University —Dayton, OH
- Vital signs
- Mid-level
- Bachelor's degree
Clinical Research Coordinator III - Mayerson Center
Cincinnati Children's Hospital —Cincinnati, OH
- $56,784.00 - $62,150.40 a year
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
Clinical Research Coordinator III
Cincinnati Children's Hospital —Cincinnati, OH
- $56,784.00 - $62,150.40 a year
- Full-time
- Psychiatry
- Mid-level
- Master's degree
Research Coordinator I
Cleveland Clinic —Cleveland, OH
- $20.77 - $31.68 an hour
- Full-time
- Vital signs
- Word processing
- High school diploma or GED
- Dental insurance
- Vision insurance
Clinical Research & IRB Specialist
Genesis HealthCare System —Ohio
- Full-time
- Office
- Ability to lift 50 pounds
- Computer skills
Clinical Research Coordinator Social & Behavioral Sciences I
Nationwide Children's Hospital —Columbus, OH
- Full-time
- Hospital
- Word processing
- Analysis skills
1d
Research Coordinator/Interventionist-1
Nationwide Children's Hospital —Columbus, OH
- Full-time
- Hospital
- Word processing
- Bachelor of Science
Clinical Research Assistant 2-Hematology
The Ohio State University Wexner Medical Center —Columbus, OH
- Online Application
- Background check
- Pass drug screening
- University
1d
Clinical Research Coordinator 2-Neurology
The Ohio State University Wexner Medical Center —Columbus, OH
- Online Application
- Background check
- Pass drug screening
- Mid-level
3d
Internal (site management) Clinical Research Associate
North American Science Associates, LLC. —Northwood, OH
- $56,000 - $109,000 a year
- Full-time
- Ability to walk for extended periods
- Computer literacy
- Writing skills
Quick Apply
3d
Clinical Research Coordinator
Dayton Center For Neurological Disorders Inc —Centerville, OH
- $25 - $35 an hour
- Full-time
- RN License
- Medical office experience
- Mid-level
- Profit sharing
- Disability insurance

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Clinical Research Associate II

AtriCure -
Mason, OH

Apply Now

Job Details

$85,000 - $105,000 a year

Benefits

Paid parental leave
Health insurance
On-site gym
Dental insurance
Parental leave
401(k) matching
Volunteer time off
Pet insurance

Qualifications

Microsoft Excel
ICH guidelines
Productivity software
Clinical quality assurance standards
Cross-functional collaboration
FDA regulations

Full Job Description

AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use AtriCure technologies for the treatment of Afib and reduction of Afib related complications. AtriCure's Isolator® Synergy™ Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure's AtriClip® Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. AtriCure's Hybrid AF™ Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. AtriCure's cryoICE cryoSPHERE® probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. For more information, visit AtriCure.com or follow us on Twitter @AtriCure.

We foster a culture of inclusion by embracing diverse experiences and individuals where everyone's authentic self is welcome. We offer supporting programs and resources that provide enriching and equitable opportunities for each person to contribute professionally and personally.

POSITION SUMMARY:

The Clinical Research Associate II (CRA II) will be a key contributor to AtriCure's clinical affairs department and primarily responsible for the site management of assigned clinical investigative sites. The CRA II will assist with the implementation and execution of study protocols and associated study documents for clinical trials, including clinical monitoring of AtriCure studies. This also includes the coordination of site activities from site start-up to site closure as needed. The CRA II will work closely with the Clinical Project Managers and Sr. CRAs to ensure the study is executed to meet project deliverables.

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. The CRA II will participate as needed, in study review meetings and attend scientific meetings and industry conferences as required. The CRA II will also conduct site visits including Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits, and Close Out Visits.

ESSENTIAL FUNCTIONS OF THE POSITION:

Assist Clinical Project Managers and Sr. CRAs in the study development and start-up process development of the informed consent form and internal review prior to submission to the IRB/EC. Collection of startup documentation from clinical investigational site
Verify that the investigator and research staff follow the approved protocol and all GCP procedures
Conduct weekly maintenance and management of study sites to ensure site compliance with study protocol, GCP/ICH, and applicable regulations
Conduct initial and ongoing study training of site personnel throughout the clinical study
Monitor and report to ATRC site enrollment activities
Verify that all research staff and facilities have adequate resources and qualifications and are maintained throughout the course of the study
Assist with the preparation of clinical study devices and verify the accountability of investigational devices are properly received, tracked, and secured at the study site
Ensure adverse events, concomitant medications, and inter-current illnesses are reported in accordance with the protocol on the CRF.
Communicate deviations from the protocol, SOPs, GCP, and applicable regulatory requirements to the investigator and ensure corrective action is implemented.
Review queries and assist in the resolution of DCFs.
Participate in project team meetings.
Participate in departmental development initiatives (e.g. training, SOP development/updates, etc.)
Ability to work on multiple projects as departmental priorities change

ADDITIONAL ESSENTIAL FUNCTIONS OF THE POSITION:

Regular and predictable work performance
Ability to work under fast-paced conditions
Ability to make decisions and use good judgement
Ability to prioritize various duties and multitask as required
Ability to successfully work with others
Additional duties as assigned

BASIC QUALIFICATIONS:

Bachelor's degree in a science or related technical field required or demonstrated equivalent combination of education, training and experience
Minimum two years of CRA experience
Comprehensive knowledge of ISO, GCP, ICH, FDA and other applicable regulations governing the conduct of clinical trials
Ability to manage role/responsibility independently.
Recognize problems, trends and react to resolve issue quickly and to bring effect resolution.
Experience working with electronic data capture systems
Strong attention to detail and an ability to prioritize and juggle multiple/competing issues.
Ability to create and manage key internal and external partnerships.
Excellent written and verbal communication skills.
Experienced user Microsoft Office software including WORD, Excel, and PowerPoint
Ability to travel up to 50%

PREFERRED QUALIFICATIONS:

Experience with medical device clinical trials desired but not required.
Prior experience with cardiovascular clinical trials.
Understanding of basic anatomy and physiology, electrophysiology and arrhythmias
Registered Nurse with previous clinical research experience as either a CRA or Study Coordinator.
CCRA or CCRP Certification

OTHER REQUIREMENTS:

Ability to regularly walk, sit, or stand as needed
Ability to occasionally bend and push/pull as needed
Ability to pass pre-employment drug screen and background check

#LI-KN1 #REMOTE

AtriCure has a variety of benefits available for US based employees and their families. Examples include Medical & Dental beginning day 1 of employment, 401K plus match, 30 days of paid Parental Leave, in addition to maternity leave, for new moms and dads, Volunteer Time off, Pet Insurance, and more. Corporate-based employees also have full access to our on-site fitness center and cafeteria. To see a complete list of our benefits, please visit our careers website: https://www.atricure.com/careers-atricure/benefits.

AtriCure participates in the federal E-Verify program to confirm the identity of and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here https://www.e-verify.gov AtriCure is an Equal Employment Opportunity/Affirmative Action employer and provides Drug Free Workplaces. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national or ethnic origin, age, protected veteran status, status as an individual with disability, sexual orientation, gender identity or any other characteristic protected by federal, state, or local law(s).

You may access our global privacy policy here: https://www.atricure.com/privacy

Apply Now

Refine Your Search

clinical research jobs in ohio

Clinical Research Associate II

Clinical Research Coordinator I

Clinical Research Coordinator

Clinical Research Coordinator-Clinical Trials Management Office

Clinical Research Scientist

Clinical Research Coordinator I - RI Behav Trials Off

Clinical Research Coordinator - Cincinnati, OH

Clinical Research Regulatory Specialist II, Seidman Cancer Center (Hybrid)

Clinical Research Quality Assurance Specialist, Seidman Cancer Center (Hybrid)

Clinical Research Coordinator

Clinical Research Coordinator III - Mayerson Center

Clinical Research Coordinator III

Research Coordinator I

Clinical Research & IRB Specialist

Clinical Research Coordinator Social & Behavioral Sciences I

Research Coordinator/Interventionist-1

Clinical Research Assistant 2-Hematology

Clinical Research Coordinator 2-Neurology

Internal (site management) Clinical Research Associate

Clinical Research Coordinator

I want to receive the latest job alert for clinical research in ohio

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