Senior Clinical Research Associate - Remote

1001 Syneos Health, LLC; United States; A distancia; USD 85.000 - 110.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health benefits

Company car or car allowance

401k with company match

Employee Stock Purchase Plan

Commissions/bonus eligibility

Flexible PTO and sick time

Descripción de la vacante

Syneos Health seeks an Experienced Clinical Research Associate (CRA) with at least 1 year of independent monitoring experience for a homebased role in the United States. The candidate will perform site qualification, initiation, monitoring, and close-out visits, ensuring GCP compliance and data integrity.

Responsibilities include evaluating site performance, escalating issues, maintaining regulatory knowledge, and supporting site enrollment and data capture.

Formación

• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Must demonstrate good computer skills and be able to embrace new technologies.
• Excellent communication, presentation and interpersonal skills.
• Ability to manage required travel of up to 75% on a regular basis.

Responsabilidades

• Performs site qualification, initiation, interim monitoring, and close-out visits (on-site or remotely).
• Evaluates site and staff performance and escalates issues with action plans.
• Maintains knowledge of ICH/GCP guidelines and SOPs.
• Verifies informed consent process and protects subject confidentiality.
• Supports subject recruitment and data tracking in tracking systems.
• Acts as liaison with study site personnel as needed.

Conocimientos

Communication

Presentation skills

Interpersonal skills

Travel up to 75%

Educación

Bachelor’s degree or RN in related field

Descripción del empleo

Syneos Health seeks an Experienced Clinical Research Associate (CRA) with at least 1 year of independent monitoring experience for a homebased role in the United States. The candidate will perform site qualification, initiation, monitoring, and close-out visits, ensuring GCP compliance and data integrity.

Responsibilities include evaluating site performance, escalating issues, maintaining regulatory knowledge, and supporting site enrollment and data capture.