Clinical Research Coordinator - Trials & Data (In-Person)

No Resistance Consulting Group, LLC.; Baton Rouge (LA); On-site; USD 30,000 - 34,000; Full time

Benefits offered by this job

401(k)

Dental Insurance

Health Insurance

Paid time off

Vision Insurance

Job summary

No Resistance is seeking motivated individuals to join our clinical research team in Baton Rouge. This full-time role focuses on the implementation and execution of trials, ensuring quality, safety, regulatory compliance, and financial objectives are met.

No prior clinical trial experience is required; on-the-job training is provided. Hours are Monday to Friday, 8:30 am to 5:00 pm, with in-person work at our Baton Rouge site.

Qualifications

• Maintaining regulatory binders and inventory of study supplies.
• Recruiting and enrolling study subjects.
• Obtaining informed consent.
• Collecting nasal swab samples and performing tests on PCR analyzers.
• Data collection, entry and query resolution.
• Ensuring protocol compliance and efficient workflow.

Responsibilities

• Maintaining regulatory binders, inventory of study-specific and clinical supplies.
• Recruiting, and enrolling study subjects.
• Obtaining informed consent.
• Collecting nasal swab samples.
• Testing samples on investigational laboratory PCR analyzers.
• Data collection and entry.
• Query resolution.
• Ensuring protocol compliance and efficient workflow including organizing clinical work areas, tracking and ordering study supplies and shipping materials, checking and replacing expired items, etc.

Job description

No Resistance is seeking motivated individuals to join our clinical research team in Baton Rouge. This full-time role focuses on the implementation and execution of trials, ensuring quality, safety, regulatory compliance, and financial objectives are met.

No prior clinical trial experience is required; on-the-job training is provided. Hours are Monday to Friday, 8:30 am to 5:00 pm, with in-person work at our Baton Rouge site.