Job Requirements
Minneapolis, MN
DoE Q or L Polygraph Unspecified
Career Level not specified
Salary not specified
Join Premium to unlock estimated salaries 
Job Description
Title: Senior Clinical Research Associate-Medical Device
Pay: Starting at $110,000, DOE
FT or PT: Full-time, Contract-to-hire (about 3 months to conversion)
Location: Remote with domestic travel (25-50% anticipated)
Kelly® Science & Clinical is seeking a Senior Clinical Research Associate for a temp-to-hire position at an early-stage, innovation-driven medical device client. If you're passionate about supporting high-impact clinical studies and improving patient care in surgical settings, and are ready to take the next step in your career, trust The Experts at Hiring Experts.
As a Senior Clinical Research Associate, you will be responsible for overseeing the execution of clinical trials from site start-up to site closure, ensuring compliance with study protocols, regulatory requirements, and maintaining quality documentation. Key responsibilities include coordinating and conducting site qualification, initiation, and monitoring visits; managing site operations; reviewing informed consent procedures; assessing investigational product accountability; and supporting the development of study documentation and site-facing presentation materials. You will develop strong relationships with clinical site staff, proactively identify and mitigate risks, and facilitate timely communication among stakeholders.
Requirements:
10338188
Pay: Starting at $110,000, DOE
FT or PT: Full-time, Contract-to-hire (about 3 months to conversion)
Location: Remote with domestic travel (25-50% anticipated)
Kelly® Science & Clinical is seeking a Senior Clinical Research Associate for a temp-to-hire position at an early-stage, innovation-driven medical device client. If you're passionate about supporting high-impact clinical studies and improving patient care in surgical settings, and are ready to take the next step in your career, trust The Experts at Hiring Experts.
As a Senior Clinical Research Associate, you will be responsible for overseeing the execution of clinical trials from site start-up to site closure, ensuring compliance with study protocols, regulatory requirements, and maintaining quality documentation. Key responsibilities include coordinating and conducting site qualification, initiation, and monitoring visits; managing site operations; reviewing informed consent procedures; assessing investigational product accountability; and supporting the development of study documentation and site-facing presentation materials. You will develop strong relationships with clinical site staff, proactively identify and mitigate risks, and facilitate timely communication among stakeholders.
Requirements:
- Bachelor's Degree or higher in healthcare or science related field (alternately, relevant experience may be considered)
- Minimum 5 years' experience as a Clinical Research Associate
- At least 3 years of monitoring Class III medical device trials
- Proficiency with Epic required
- Thorough knowledge of clinical research concepts, FDA regulations, and Good Clinical Practice (GCP)
- Strong organizational, communication, and critical thinking skills
- Willingness and ability to travel domestically 25-50% of the time
- Experience in breast cancer, breast reconstruction, or related therapeutic areas preferred
- Proficient in Microsoft Office and comfortable learning new clinical trial management systems
10338188
group id: 10117306