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Research Assistant Jobs
Company | Reno Orthopedic Center |
Address | Reno, NV, United States |
Employment type | FULL_TIME |
Salary | |
Category | Technology, Information and Internet |
Expires | 2023-06-08 |
Posted at | 1 year ago |
As a Research Assistant, you would be crucial to our mission because you would be responsible for facilitating daily clinical trial activities, gathering and analyzing data, and writing reports in a manner that places emphasis on quality research studies. On any given day, you could interact with patients, work with study participants, and monitor research protocols. If you value respect, optimism, compassion, innovation, and top-notch patient care, you have found your home.
Be a part of our family and contribute to your community in a real and tangible way. Apply now to be a part of something fantastic!
What would you do as a Research Assistant?
You can expect to regularly:
Education/Certifications
This position operates in a professional office environment.
Physical: The noise level is usually moderate.
Travel: May require up to 10% travel to and from other locations, including sponsor study training meetings.
Benefits
Check out our home page by clicking on “View all jobs” to explore the many benefits ROC provides to employees! This position is eligible for Full Time benefits.
Be a part of our family and contribute to your community in a real and tangible way. Apply now to be a part of something fantastic!
What would you do as a Research Assistant?
You can expect to regularly:
- Participate with PI and study team to identify and prioritize the development of systems and infrastructure to maintain research quality and compliance.
- Determine eligibility and consent of study participants according to protocol;
- Provide accurate and timely data collection, documentation, entry, and reporting in both sponsor and ROC Foundation databases;
- Communicate specific study requirements to the research team, including internal and external parties, sponsor, monitors, Principal Investigator (PI), and study participants;
- Ensure assigned studies comply with good clinical practice, research protocols, the Food and Drug Administration (FDA) and the Office for Human Research Protections (OHRP) and report any concerns or issues to supervisor immediately;
- Maintain regulatory documents in accordance with ROC Foundation Standard Operating Procedures (SOP’s) and applicable regulations;
- Communicate and interact directly with patients for scheduling visits, tele-check ins, and in-person patient visits;
Education/Certifications
- High School Diploma/GED;
- Basic knowledge of medical terminology;
- Basic knowledge of HIPAA policies and procedures;
- Good knowledge of Microsoft Office Suite including MS Word and MS Excel;
- Communicating effectively with others
- Performing duties with high attention to detail including reviewing work and correcting errors;
This position operates in a professional office environment.
Physical: The noise level is usually moderate.
Travel: May require up to 10% travel to and from other locations, including sponsor study training meetings.
Benefits
Check out our home page by clicking on “View all jobs” to explore the many benefits ROC provides to employees! This position is eligible for Full Time benefits.
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