Clinical Research Coordinator

SQRL; Marrero (LA); On-site; USD 55,000 - 65,000; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Paid maternity leave

Paid paternity leave

Tuition assistance

Disability insurance

Job summary

A growing clinical research organization is seeking an Associate Director of Recruiting in Marrero, LA. The role involves supporting clinical trials, conducting patient procedures, and managing recruitment. Ideal candidates have 1+ years of CRC experience, including phlebotomy, and must work on-site during the week. A competitive salary of $55,000 - $65,000 with full benefits is offered.

Qualifications

• 1+ years of experience working as a CRC on sponsor backed clinical trials.
• Ability to work on site M-F (no remote or hybrid).
• Must perform phlebotomy without supervision.

Responsibilities

• Conduct procedures such as vital signs, blood draws, EKGs, and bladder scans.
• Support patient recruitment, enrollment, scheduling, and consent.
• Manage lab procedures and shipments.

Skills

Phlebotomy experience

Clinical trial coordination

Patient recruitment

Job description

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

• $55,000 - $65,000 salary + full benefits
• M - F schedule, no weekends or late nights!
• Tons of growth potential to Sr. CRC, Lead CRC, Site Manager, and more!

The Company

Our client is a fast growing clinical research site network that started in 2015 and grew to 11 sites with plans to double in the next couple years! They have run over 400 clinical studies in Phase I - IV in therapeutic areas mainly focused in GI, Hepatology, and CNS! Their goal is to be the best place to work in the country, and they are excited to find people excited to make that vision come to life through quality patient care and research.

Responsibilities

As a CRC 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, and bladder scans.
• Patient recruitment, enrollment, scheduling, and consent
• Lab procedures and shipments
• Maintain GCP and follow protocols
• Data management in EDC systems
• Overall coordination of the study

Qualifications:

• 1+ years of experience working as a CRC on sponsor backed clinical trials
• Phlebotomy experience (ability to perform without supervision)
• 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)

Paid maternity leave

Paid paternity leave

Tuition assistance

Disability insurance

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