Senior Clinical Research Associate - Remote & Impactful Trials

Syneos Health/ inVentiv Health Commercial LLC; Fargo (ND); On-site; USD 70,000 - 110,000; Full time

Benefits offered by this job

Company car/allowance

Health benefits

401(k) plan

Stock purchase plan

Bonus eligibility

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate - Sponsor Dedicated to monitor trial sites across regulatory and protocol requirements. You will perform site qualification, initiation, interim monitoring and close-out visits, either on-site or remotely, ensuring data integrity and patient safety.

Travel up to 75% is required. The role emphasizes site management, IP handling, ISF/TMF reconciliation, and collaboration with cross-functional teams to support audit readiness and

Qualifications

• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Must demonstrate good computer skills and be able to embrace new technologies.
• Excellent communication, presentation and interpersonal skills.
• Ability to manage required travel up to 75% on a regular basis.

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management and close-out visits, on-site or remotely, ensuring regulatory, ICH‑GCP and GPP compliance.
• Verifies informed consent process and protects subject confidentiality; assesses safety and data integrity.
• Reviews site processes, performs Source Document Review, ensures accurate data entry in CRFs, and drives query resolution.
• Manages IP inventory, storage, labeling, import/release per protocol and regulatory requirements.
• Maintains ISF and TMF accuracy; archives essential documents per guidelines.
• Supports recruitment, retention and awareness strategies; tracks observations and action items in systems.
• Allocates project scope, budgets and timelines; adapts to changing priorities to meet objectives.

Skills

Excellent communication

Travel willingness

Education

Bachelor's degree or RN

Job description

Syneos Health is seeking an Experienced Clinical Research Associate - Sponsor Dedicated to monitor trial sites across regulatory and protocol requirements. You will perform site qualification, initiation, interim monitoring and close-out visits, either on-site or remotely, ensuring data integrity and patient safety.

Travel up to 75% is required. The role emphasizes site management, IP handling, ISF/TMF reconciliation, and collaboration with cross-functional teams to support audit readiness and