Senior Clinical Research Associate - Remote/Onsite

Syneos Health/ inVentiv Health Commercial LLC; Colorado; On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health benefits including Medical, Dental, and Vision

401k company match

Flexible paid time off (PTO)

Job summary

Syneos Health/ inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate dedicated to managing sites throughout clinical trials. The role requires expertise in site qualification, regulatory compliance, and patient confidentiality. You will be instrumental in ensuring that studies are conducted as per guidelines and protocols, maximizing patient data integrity.

This position emphasizes strong communication skills, the ability to handle complex situations, and a commitment to adherence to ICH/GCP standards. As part of a dynamic team, you will collaborate closely with site staff and be a vital link between them and the project management team.

Qualifications

• Bachelor's degree or RN in a related field or equivalent combination of education, training and experience.
• Knowledge of Good Clinical Practice/ICH Guidelines.
• Excellent communication, presentation and interpersonal skills.
• Ability to manage required travel of up to 75%.

Responsibilities

• Performs site qualification, initiation, monitoring, management, and close-out visits.
• Verifies informed consent process and documentations for subjects/patients.
• Documents activities via confirmation letters, reports, and communication logs.
• Acts as primary liaison with study site personnel.

Skills

Excellent communication skills

Knowledge of Good Clinical Practice/ICH Guidelines

Good computer skills

Education

Bachelor's degree or RN in a related field

Job description

Syneos Health/ inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate dedicated to managing sites throughout clinical trials. The role requires expertise in site qualification, regulatory compliance, and patient confidentiality. You will be instrumental in ensuring that studies are conducted as per guidelines and protocols, maximizing patient data integrity.

This position emphasizes strong communication skills, the ability to handle complex situations, and a commitment to adherence to ICH/GCP standards. As part of a dynamic team, you will collaborate closely with site staff and be a vital link between them and the project management team.