Senior Clinical Research Associate – Remote/Onsite

Syneos Health, Inc.; Lincoln (NE); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits (Medical, Dental, and

Vision

401k with company match

Employee Stock Purchase Plan

Performance-based bonus

Flexible PTO

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate to support regionally aligned activities across the US. You will monitor sites, manage documentation, and ensure adherence to ICH-GCP, SOPs, and study protocols.

The role emphasizes site qualification, monitoring, data integrity, and collaboration with sponsor teams. Travel up to 75% is expected, with competitive benefits and professional development opportunities.

Qualifications

• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Excellent communication, presentation and interpersonal skills.
• Ability to manage required travel of up to 75% on a regular basis.
• US ONLY: Site access information may be requested as part of employment.

Responsibilities

• Performs site qualification, initiation, monitoring, management and close-out visits (on-site or remote) ensuring regulatory, ICH-GCP and/or GPP compliance.
• Verifies informed consent processes and protects subject confidentiality; assesses safety and data integrity factors.
• Assesses site processes; conducts Source Document Review and ensures CRF data accuracy.
• May perform IP inventory, reconciliation and verify IP dispensing per protocol.
• Maintains ISF accuracy and reconciliation with TMF; archives essential documents as required.
• Supports recruitment, data tracking and action item resolution; ensures timelines are met.

Skills

GCP/ICH guidelines knowledge

Communication skills

Travel readiness

Computer skills

Education

Bachelor's degree or RN in related field

Job description

Syneos Health is seeking an Experienced Clinical Research Associate to support regionally aligned activities across the US. You will monitor sites, manage documentation, and ensure adherence to ICH-GCP, SOPs, and study protocols.

The role emphasizes site qualification, monitoring, data integrity, and collaboration with sponsor teams. Travel up to 75% is expected, with competitive benefits and professional development opportunities.