Senior Clinical Research Associate - Site Management

Syneos Health/ inVentiv Health Commercial LLC; Santa Monica (CA); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits (Medical, Dental, and.

401k / Retirement savings

Employee Stock Purchase Plan

Bonus eligibility

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate to support sponsor-delivered programs with on-site and remote monitoring. You will perform site qualification, initiation, interim monitoring, and close-out visits, ensuring regulatory compliance across trials.

Collaborate with site staff and sponsor teams, manage data quality, and participate in investigator meetings. Expect up to 75% travel in the United States and cross-functional collaboration across therapeutic areas.

Qualifications

• Bachelor's degree or RN in a related field is required.
• Knowledge of Good Clinical Practice/ICH guidelines and regulatory requirements.
• Excellent communication, presentation and interpersonal skills.
• Ability to travel up to 75% on a regular basis.

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management and close-out visits (on-site or remote), ensuring ICH-GCP and/or GPP compliance.
• Verifies informed consent processes and protects subject confidentiality.
• Conducts source data review and query resolution to ensure data quality and Timelines.
• Manages IP inventory and ensures correct labeling, storage and accountability.
• Maintains ISF and TMF accuracy and coordinates archiving per regulations.
• Documents activities and supports recruitment and retention strategies; data entry into tracking systems.
• Collaborates with sponsor and site personnel; trains site team members; supports audit readiness.

Skills

Excellent communication

Presentation skills

Interpersonal skills

Computer skills

Travel up to 75%

Education

Bachelor's degree or RN

Job description

Syneos Health is seeking an Experienced Clinical Research Associate to support sponsor-delivered programs with on-site and remote monitoring. You will perform site qualification, initiation, interim monitoring, and close-out visits, ensuring regulatory compliance across trials.

Collaborate with site staff and sponsor teams, manage data quality, and participate in investigator meetings. Expect up to 75% travel in the United States and cross-functional collaboration across therapeutic areas.