Senior Clinical Research Associate II - Site Management

Syneos Health; Minnesota; On-site; USD 65,000 - 90,000; Full time

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate to support sponsor-dedicated trials in the United States. You will lead site qualification, initiation, monitoring, and close-out visits, ensuring GCP compliance, data integrity, and patient safety across trial sites.

Strong communication and travel readiness are essential. The role emphasizes collaboration with cross-functional teams, site management, and adherence to regulatory requirements while advancing innovative therapies

Qualifications

• Bachelor’s degree or RN required or equivalent.
• Knowledge of Good Clinical Practice/ICH guidelines.
• 2 years of monitoring experience required.
• Strong communication and interpersonal skills.

Responsibilities

• Performs site qualification, initiation, monitoring and close-out visits on-site or remotely.
• Ensures regulatory, ICH-GCP and protocol compliance with SOPs.
• Verifies informed consent and protects subject confidentiality.
• Supports site data validation, query resolution and data integrity.
• Manages IP inventory, labeling and distribution per protocol.
• Maintains ISF and TMF alignment and supports audit readiness.

Skills

GCP knowledge

Monitoring experience

Excellent communication

Computer skills

Ability to travel

Education

Bachelor’s degree or RN

Job description

Syneos Health is seeking an Experienced Clinical Research Associate to support sponsor-dedicated trials in the United States. You will lead site qualification, initiation, monitoring, and close-out visits, ensuring GCP compliance, data integrity, and patient safety across trial sites.

Strong communication and travel readiness are essential. The role emphasizes collaboration with cross-functional teams, site management, and adherence to regulatory requirements while advancing innovative therapies