Remote Clinical Research Associate II - Sponsor Focus

Syneos Health, Inc.; Kansas; Hybrid; USD 75,000 - 110,000; Full time

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate for a sponsor-dedicated role. This remote-friendly position supports sites across the United States and requires up to 75% travel.

The CRA will monitor, manage, and quality-check trial sites to ensure regulatory compliance and data integrity. Ideal candidates have a healthcare degree (Bachelor’s or RN), strong GCP knowledge, and excellent communication skills.

Qualifications

• Bachelor’s degree or RN in a related field.
• Knowledge of Good Clinical Practice/ICH Guidelines.
• Excellent communication, presentation and interpersonal skills.
• Good computer skills and adaptability to new technologies.
• Ability to travel up to 75% regularly.

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management and close-out visits (on-site or remotely) ensuring regulatory, ICH-GCP and/or GPP compliance.
• Verifies informed consent and protects subject confidentiality; assesses safety and data integrity factors.
• Reconciles ISF with TMF and ensures proper archiving per local guidelines.
• Documents activities via letters, reports, and logs; supports recruitment and data tracking.
• Manages project scope, budgets, and timelines at site level and communicates effectively.
• Acts as liaison with study site personnel and ensures training and compliance.
• Prepares for Investigator Meetings and sponsor meetings; participates in global meetings.
• Provides guidance toward audit readiness and supports follow-up actions.
• Maintains knowledge of ICH/GCP guidelines and completes required training.

Skills

Bachelor’s degree or RN

Good computer skills

Excellent communication

75% travel

GCP/ICH knowledge

Education

Bachelor’s degree or RN in related field

Job description

Syneos Health is seeking an Experienced Clinical Research Associate for a sponsor-dedicated role. This remote-friendly position supports sites across the United States and requires up to 75% travel.

The CRA will monitor, manage, and quality-check trial sites to ensure regulatory compliance and data integrity. Ideal candidates have a healthcare degree (Bachelor’s or RN), strong GCP knowledge, and excellent communication skills.