Clinical Research Coordinator

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

Job Location:

Baton Rouge

Expected Start Date:

October

Company Description:

Headquartered in Birmingham, No Resistance is a clinical trial site management organization that performs clinical trials in urgent care centers throughout the north and southeast. We focus on sample collection and testing trials for lab device manufacturers with the purpose of collecting data to support the device's 510(k) or emergency use approval by the FDA. Notably, the trials we have participated in have directly led to the FDA EUA approval of three separate COVID-19 PCR testing platforms.

No clinical trial experience is required. No Resistance will train the right candidate(s). Hours are Monday-Friday 8:30 am to 5:00 pm with no weekend requirements. Hours will depend on Clinic hours and clinical trial needs.

Job Description:

No Resistance is seeking motivated individuals to join our team! In this role, you'll play a pivotal part in the implementation and execution of clinical research projects, ensuring the successful attainment of quality, safety, regulatory, and financial objectives.

Job Duties:

• 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.
• Assuring protocol compliance and efficient workflow including organizing clinical work areas, tracking and ordering study supplies and shipping materials, checking and replacing expired items, etc.

Key Success Factors:

• Ability to work independently.
• Desire to work in a clinical environment with direct patient contact.
• Genuine interest in research.
• Timely in all communications.
• Superior attention to detail.

While not a requirement, senior pre-medical students who hope to gain experience in clinical research or recent graduates who have a "gap" year before they start medical school are encouraged to apply. This position offers an exceptional opportunity to earn a competitive income while gaining invaluable experience highly regarded by medical school admission committees.

Job Type: Full-time

Pay: $22.50-$25.00 per hour

Expected hours: 40 per week

Benefits:

• 401(k)
• Dental Insurance
• Health Insurance
• Paid time off
• Vision Insurance

Schedule:

• Monday to Friday

Work Location: In person