Remote CRA: Full-Service Clinical Trials

Syneos Health, Inc.; North Dakota; Hybrid; USD 65,000 - 95,000; Full time

Benefits offered by this job

Company car/Car allowance

Health benefits (Medical, Dental, and

Company match 401k

Employee Stock Purchase Plan

Commission/Bonus eligibility

Flexible PTO and sick time

Job summary

Syneos Health, Inc. is seeking a Clinical Research Associate - Full-Service to support remote monitoring and site management across diverse trials with strong adherence to ICH-GCP and data integrity. You will collaborate with sites and project teams to ensure regulatory compliance and quality deliverables.

Qualifications include a Bachelor’s degree or RN and excellent communication skills. The role requires up to 75% travel and a proactive approach to study start-up, monitoring, and close-out

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 regulatory requirements.
• Excellent communication, presentation and interpersonal skills.

Responsibilities

• Performs site qualification, 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 and protects confidentiality; assesses factors affecting subject safety and data integrity.
• Reviews ISF/TMF and ensures archiving requirements; supports recruitment and data tracking.
• Manages IP inventory, labeling and compliance with protocol.
• Maintains site data quality; coordinates with site staff to resolve questions and timelines.
• Attends Investigator Meetings and provides audit readiness support when needed.

Skills

GCP/ICH Knowledge

Communication Skills

Willing to Travel

Computer Proficiency

Education

Bachelor’s degree or RN in related field

Job description

Syneos Health, Inc. is seeking a Clinical Research Associate - Full-Service to support remote monitoring and site management across diverse trials with strong adherence to ICH-GCP and data integrity. You will collaborate with sites and project teams to ensure regulatory compliance and quality deliverables.

Qualifications include a Bachelor’s degree or RN and excellent communication skills. The role requires up to 75% travel and a proactive approach to study start-up, monitoring, and close-out