Clinical Research Nurse

SQRL; Columbus (OH); On-site; USD 65,000 - 70,000; Full time

Job summary

SQRL is seeking an Associate Director of Recruiting to join their clinical research team in Columbus, Ohio. The position is ideal for candidates willing to learn and work hands-on in a supportive, patient-centric environment. This role offers a competitive salary range of $65,000 - $70,000 with consistent schedules and benefits, making it a unique opportunity in the healthcare and clinical research industry.

Benefits

Medical insurance

Vision insurance

401(k)

Qualifications

• Willingness to work hands-on and learn clinical research.
• Ability to work on-site M-F with no remote options.

Responsibilities

• Conduct procedures such as vital signs, blood draws, EKGs, bladder scans.
• Manage patient recruitment, enrollment, and consent.
• Coordinate daily clinical trial activities and support patients.

Skills

Willingness to work hands on

Job description

1 week ago Be among the first 25 applicants

This range is provided by SQRL. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Associate Director of Recruiting at SQRL | Clinical Research, Healthcare, Biotech, Life Sciences

Highlights

• $65,000 - $70,000 salary + benefits!
• Unique opportunity to step into the clinical research industry - no prior research experience required!
• Consistent schedule, no overnights or weekends, flex holidays, and more!
• Work with a company that truly cares about their employees and patients

About Our Client

Our client is a long standing clinical research site in the Columbus, OH area that takes a truly unique patient-centric, service-oriented, approach to clinical research. Their reputation for excellence has been built across over 20 therapeutic areas, over 15 physicians, and over 550 completed trials. They are looking to expand their team with a skilled RN seeking to get into the clinical research industry!

Responsibilities

As a Clinical Research Nurse, you will be a specialized research professional under the direction of the clinical Principal Investigator and Site Manager. While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical trial process!

• Conduct procedures such as vital signs, blood draws, EKGs, bladder scans, and infusions
• Patient recruitment, enrollment, and consent
• Lab procedures, processing, and shipments
• Maintain GCP and follow research protocols
• Data management in EDC systems
• Communication with sponsors and vendors on trial activities and patient care
• Overall coordination of the study

Qualifications:

• Willingness to work hands on and learn clinical research!
• Ability to work on site M-F on site (there is no remote or hybrid days)

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research

• Industries

  Research Services

Referrals increase your chances of interviewing at SQRL by 2x

Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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