Clinical Research Coordinator - In-Person | Great Benefits

No Resistance Consulting Group, LLC; Baton Rouge (LA); In loco; USD 30.000 - 34.000; Tempo pieno

Vantaggi offerti da questo lavoro

401(k)

Dental Insurance

Health Insurance

Paid time off

Vision Insurance

Descrizione del lavoro

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

Competenze

• 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.

Mansioni

• 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.

Conoscenze

Clinical research

Data entry

Regulatory compliance

Informed consent

Strumenti

PCR analyzers

Inventory management

Descrizione del lavoro

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