Senior Clinical Research Associate – Remote/On‑Site

Syneos Health/ inVentiv Health Commercial LLC; Morrisville (NC); On-site; USD 75,000 - 110,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits

401k match

Employee Stock Purchase Plan

Bonus/commissions

Flexible PTO and sick time

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate to support sponsor-dedicated trials. The role involves site qualification, initiation, monitoring, and close-out visits, performed on-site or remotely, with emphasis on regulatory compliance and data integrity.

You will verify informed consent, protect patient confidentiality, and resolve data queries using SDV techniques. Travel up to 75% is required, with strong communication and computer skills to coordinate with sites and

Qualifications

• Bachelor's degree or RN required
• Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements
• Excellent communication, presentation and interpersonal skills
• Ability to travel up to 75% regularly
• US deployment to sites may be required for access and compliance

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management and close-out visits, on-site or remotely, ensuring regulatory and protocol compliance.
• Verifies informed consent process and protects subject confidentiality.
• Reviews site data, performs source data verification, and resolves data queries to closure per timelines.
• Manages IP inventory, labeling, storage and release per protocol.
• Maintains ISF/TMF accuracy and archiving requirements; supports recruitment and data tracking.
• Communicates with site staff, prepares for Investigator Meetings and sponsor meetings.
• Supports audit readiness and training of site personnel; stays updated on ICH/GCP guidelines.

Skills

Excellent communication

Travel up to 75%

Proficient computer skills

Education

Bachelor's degree or RN

Job description

Syneos Health is seeking an Experienced Clinical Research Associate to support sponsor-dedicated trials. The role involves site qualification, initiation, monitoring, and close-out visits, performed on-site or remotely, with emphasis on regulatory compliance and data integrity.

You will verify informed consent, protect patient confidentiality, and resolve data queries using SDV techniques. Travel up to 75% is required, with strong communication and computer skills to coordinate with sites and