Top 173 Scientist Jobs in Mason Oh

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
Medical Laboratory Scientist I - Microbiology
Quest Diagnostics —Cincinnati, OH
- From $33 an hour
- Weekends as needed
- OSHA
- Bachelor of Science
- HIPAA
- Employee stock purchase plan
- Disability insurance
Quick Apply
Technician Laboratory
Coca-Cola Consolidated, Inc. —Cincinnati, OH
- $28.36 an hour
- Computer literacy
- Ability to climb stairs
- High school diploma or GED
- Health insurance
8d
Quality Scientist
Merck KGaA —Miamisburg, OH
- $64,900 - $107,900 a year
- Basic math
- Master's degree
- Analysis skills
- Health insurance
- Paid time off
Analyst II, QC Microbiology
Resilience US, LLC —West Chester, OH
- $60,000 - $86,250 a year
- Full-time
- Mid-level
- Bachelor's degree
- US work authorization
- Paid holidays
- Disability insurance
Quick Apply
Lab Associate
LyondellBasell Industries —Cincinnati, OH
- Email
- 18 years or older
- Associate's degree
- Communication skills
- Health insurance
Quality Scientist
EMD-Merck US —Miamisburg, OH
- $64,900 - $107,900 a year
- Basic math
- Master's degree
- Analysis skills
- Health insurance
- Paid time off
Quick Apply
QC Scientist I / Data Review
Thermo Fisher Scientific —Cincinnati, OH
- Weekends as needed
- Background check
- Computer literacy
- Pass drug screening
10d
Associate Production Scientist
Merck KGaA —Miamisburg, OH
- $23 - $42 an hour
- Mid-level
- Ability to lift 50 pounds
- Analysis skills
- Health insurance
- Paid time off
Process Research Lab Associate Researcher
Procter & Gamble —Cincinnati, OH
- $61,600 - $70,850 a year
- Full-time
- Microsoft Outlook
- High school diploma or GED
- US work authorization
Medical Laboratory Scientist II
Quest Diagnostics —Cincinnati, OH
- From $34.50 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Bachelor of Science
- Employee stock purchase plan
- Disability insurance
Quick Apply
Production Scientist
EMD-Merck US —Miamisburg, OH
- $74,500 - $122,200 a year
- Full-time
- 5 years
- Master's degree
- Bachelor's degree
- Health insurance
- Paid time off
Quick Apply
Geologist/Environmental Scientist - Entry Level
Tetra Tech —Cincinnati, OH
- 8 hour shift
- Background check
- Bachelor of Science
- Office
- Health savings account
- AD&D insurance
Materials Laboratory Technician
METCUT RESEARCH ASSOC —Cincinnati, OH
- Full-time
- Microsoft Excel
- Pass drug screening
- Windows
- Disability insurance
- Health insurance
Quick Apply
Olfactive Scientist, Beauty Fragrances
Procter & Gamble —Mason, OH
- $85,000 - $122,200 a year
- Online Application
- Office
- Travel
- Communication skills
5h
Senior Analyst, QC Microbiology
Resilience US, LLC —West Chester, OH
- $75,000 - $116,250 a year
- Full-time
- 5 years
- Mid-level
- Bachelor's degree
- Paid holidays
- Disability insurance
Quick Apply
General Helper- Materials Lab - Part Time
METCUT RESEARCH ASSOC —Cincinnati, OH
- Part-time
- High school diploma or GED
- Entry level
Quick Apply
7d
Chemistry Data Validator / Analytical Coordinator
GHD —West Chester, OH
- $60,500 - $80,700 a year
- Hybrid work
- Office
- Organizational skills
- Senior level
- Paid holidays
- Paid time off
Clinical Research Coordinator - Cincinnati, OH
IQVIA —Cincinnati, OH
- $35 - $42 an hour
- Part-time
- Vital signs
- Office
- Bachelor's degree
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

scientist jobs in mason oh

Clinical Research Associate II

Medical Laboratory Scientist I - Microbiology

Technician Laboratory

Quality Scientist

Analyst II, QC Microbiology

Lab Associate

Quality Scientist

QC Scientist I / Data Review

Associate Production Scientist

Process Research Lab Associate Researcher

Medical Laboratory Scientist II

Production Scientist

Geologist/Environmental Scientist - Entry Level

Materials Laboratory Technician

Olfactive Scientist, Beauty Fragrances

Senior Analyst, QC Microbiology

General Helper- Materials Lab - Part Time

Chemistry Data Validator / Analytical Coordinator

Clinical Research Coordinator - Cincinnati, OH

Clinical Research Coordinator

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