Remote Clinical Research Associate: Site Monitoring & Oversight

Syneos Health, Inc.; Montgomery (AL); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits including Medical, +3

Company match 401k

Employee Stock Purchase Plan

Eligible for commissions/bonus

Flexible PTO and sick time

Job summary

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to work across the US in a regionally aligned role.

The position focuses on site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance, with on-site or remote execution as needed. The CRA will verify informed consent, protect patient confidentiality, review source documents, and support data integrity through CRF entry and query resolution.

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 and other applicable regulatory requirements.
• Excellent communication, presentation and interpersonal skills.
• Ability to manage required travel of up to 75% on a regular basis.

Responsibilities

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (on-site or remote) ensuring regulatory, ICH-GCP and/or GPP and protocol compliance.
• Verifies informed consent process and protects confidentiality of subjects.
• Conducts Source Document Review and verifies data in case report forms; drives query resolution to closure.
• May manage IP inventory and ensure proper labelling, storage and release/return per protocol.

Skills

GCP/ICH Knowledge

Strong communication

Willingness to travel

Computer skills

Education

Bachelor's degree or RN in a related field or equivalent combination of education, training and experience

Job description

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to work across the US in a regionally aligned role.

The position focuses on site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance, with on-site or remote execution as needed. The CRA will verify informed consent, protect patient confidentiality, review source documents, and support data integrity through CRF entry and query resolution.