Clinical Research Coordinator

No Resistance Consulting Group, LLC; Baton Rouge (LA); Vor Ort; USD 30.000 - 34.000; Vollzeit

Benefits dieser Stelle

401(k)

Dental Insurance

Health Insurance

Paid time off

Vision Insurance

Zusammenfassung

No Resistance Consulting Group, LLC in Baton Rouge, LA is seeking motivated individuals for a full-time, on-site clinical research role. You will support the implementation and execution of projects, ensure quality, safety, regulatory, and financial objectives, and work closely with study teams.

Responsibilities include maintaining regulatory binders, recruiting and enrolling subjects, obtaining informed consent, collecting nasal swabs, testing samples, data entry, and ensuring protocol

Qualifikationen

• Knowledge of regulatory requirements for clinical trials.
• Experience handling clinical study data and source documentation.
• Ability to obtain informed consent and work with study participants.

Aufgaben

• Maintaining regulatory binders and inventory for study 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.

Kenntnisse

Clinical research

Data entry

Regulatory compliance

Informed consent

Tools

PCR analyzers

Inventory management

Jobbeschreibung

Job Location:

Baton Rouge, LA

Expected Start Date:

October 26, 2026

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. Clinical research hours may be dependent on clinical study and clinic.

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