Senior Clinical Research Associate - Remote/Onsite

Syneos Health/ inVentiv Health Commercial LLC; Rhode Island; Presencial; USD 70.000 - 90.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health benefits including Medical, Dental, and Vision

Company car or car allowance

Flexibility in paid time off

Descripción de la vacante

Syneos Health/ inVentiv Health Commercial LLC is looking for an Experienced Clinical Research Associate dedicated to ensuring compliance with clinical research protocols. The role involves site qualification, interim monitoring, and maintaining data integrity across various trials.

Ideal candidates should possess a Bachelor's degree or RN in a related field, demonstrate strong communication skills, and be willing to travel up to 75%. Success in this role requires knowledge of regulatory requirements and an eagerness to embrace new technologies.

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.

Responsabilidades

• Performs site qualification, site initiation, interim monitoring, and site management activities.
• Verifies the process of obtaining informed consent has been adequately performed.
• Assesses site processes and conducts Source Document Review of appropriate site documents.
• Documents activities via confirmation letters, follow-up letters, and trip reports.
• Acts as primary liaison with study site personnel.

Conocimientos

Good Clinical Practice/ICH Guidelines

Excellent communication skills

Interpersonal skills

Ability to manage travel

Educación

Bachelor's degree or RN in a related field

Herramientas

Computer skills

Descripción del empleo

Syneos Health/ inVentiv Health Commercial LLC is looking for an Experienced Clinical Research Associate dedicated to ensuring compliance with clinical research protocols. The role involves site qualification, interim monitoring, and maintaining data integrity across various trials.

Ideal candidates should possess a Bachelor's degree or RN in a related field, demonstrate strong communication skills, and be willing to travel up to 75%. Success in this role requires knowledge of regulatory requirements and an eagerness to embrace new technologies.