Clinical Research Coordinator I – Impactful Trials

Centricity Research; Suffolk (VA); In loco; USD 42.000 - 62.000; Tempo pieno

Vantaggi offerti da questo lavoro

Health, dental, and vision insurance

Enhanced EAP - mental health support

Flexible PTO + paid holidays

Continuing education reimbursement

401(k) with company match and vesting

Descrizione del lavoro

Centricity Research in the United States is seeking a Clinical Research Coordinator I (CRC I) to support clinical studies by handling a mix of administrative and clinical tasks. You will work with Investigators and the research team to ensure visits, documentation, and regulatory compliance align with protocol requirements.

Ideal candidates have a bachelor's in health/science, 2–4 years in healthcare, and comfort with clinical tools like ECGs and blood pressure devices.

Competenze

• Bachelor's degree in health, science, or research-related field (or equivalent).
• 2–4 years of experience in a healthcare setting; comfortable with clinical tools like ECGs and BP monitors.
• Phlebotomy experience or willingness to learn where permitted by law (training provided).

Mansioni

• Conduct study visits per protocol, GCP, SOPs and regulatory requirements.
• Support recruitment, screening, enrollment, and informed consent processes.
• Complete study documentation, regulatory records, and periodic reports accurately.
• Prepare for monitoring visits, audits, and inspections; support site start-up activities.

Conoscenze

Clinical coordination

Documentation & data accuracy

Team collaboration

Communication

Multitasking in fast-paced environment

Formazione

Bachelor's degree in health, science, or research-related field

Strumenti

ECG machine

Blood pressure monitor

Vital signs equipment

Weighing scale

Descrizione del lavoro

Centricity Research in the United States is seeking a Clinical Research Coordinator I (CRC I) to support clinical studies by handling a mix of administrative and clinical tasks. You will work with Investigators and the research team to ensure visits, documentation, and regulatory compliance align with protocol requirements.

Ideal candidates have a bachelor's in health/science, 2–4 years in healthcare, and comfort with clinical tools like ECGs and blood pressure devices.