Remote Senior Clinical Research Associate – Sponsor Focus

Syneos Health, Inc.; North Dakota; Hybrid; USD 80,000 - 110,000; Full time

Benefits offered by this job

Health benefits (Medical, Dental, and

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate to support Sponsor Dedicated projects remotely in the United States. The role involves monitoring, site management, and ensuring regulatory compliance across trials, with significant travel to sites as needed.

You will verify informed consent, manage data quality, and support audit readiness while collaborating with cross-functional teams to accelerate therapy delivery for patients.

Qualifications

• Bachelor’s degree or RN in a related field required.
• Knowledge of Good Clinical Practice/ICH Guidelines and other regulatory requirements.
• Willingness to travel up to 75% on a regular basis.
• Excellent communication, presentation and interpersonal skills.
• Ability to embrace new technologies and systems.

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management and close-out visits (on-site or remote) ensuring ICH-GCP and protocol compliance; communicates issues and develops action plans.
• Verifies informed consent and protects subject safety and data integrity at sites.
• Conducts Source Document Review and data verification; guides site staff on query resolution.
• May handle IP inventory, labeling, storage, and compliance with protocol.
• Maintains ISF/TMF accuracy and supports audit readiness and regulatory documentation.

Skills

Excellent communication skills

Presentation skills

Interpersonal skills

Travel up to 75%

Good computer skills

Knowledge of GCP/ICH Guidelines

Education

Bachelor’s degree or RN in related field

Job description

Syneos Health is seeking an Experienced Clinical Research Associate to support Sponsor Dedicated projects remotely in the United States. The role involves monitoring, site management, and ensuring regulatory compliance across trials, with significant travel to sites as needed.

You will verify informed consent, manage data quality, and support audit readiness while collaborating with cross-functional teams to accelerate therapy delivery for patients.