Senior Clinical Research Associate - Sponsor-Focused

Syneos Health/ inVentiv Health Commercial LLC; Boston (MA); On-site; USD 80,000 - 110,000; Full time

Benefits offered by this job

Health benefits

Company 401k match

Stock Purchase Plan

Paid time off

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate to support sponsor-dedicated monitoring across clinical sites in the United States. The CRA will perform site qualification, initiation, monitoring, and close-out visits, ensuring GCP/ICH compliance and data integrity.

You will review informed consent, manage IP handling, ISF/TMF reconciliation, and support site staff training. Up to 75% travel, with opportunities for remote work in appropriate circumstances.

Qualifications

• Bachelor's degree or RN in a related field or equivalent
• Knowledge of GCP/ICH Guidelines and regulatory requirements
• Good computer skills and ability to embrace new technologies
• Excellent communication, presentation and interpersonal skills
• Ability to travel up to 75% regularly

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management, and close-out visits (on-site or remote) ensuring regulatory, ICH‑GCP and/or GPP and protocol compliance.
• Verifies informed consent processes and protects confidentiality; assesses factors affecting subject safety and data integrity.
• Conducts source document review and data verification for CRFs; drives query resolution to closure.
• Manages investigational product inventory, storage, labeling, and administration per protocol.
• Reconciles ISF with TMF and ensures archiving per local guidelines; supports recruitment and data tracking.
• Communicates with site staff, provides guidance, and trains team members; ensures timelines and budgets are met.
• Attends Investigator Meetings and sponsor meetings; supports audit readiness and follow-up actions.

Skills

GCP/ICH knowledge

Communication skills

Computer skills

Travel readiness

Collaborative mindset

Education

Bachelor's degree or RN

Job description

Syneos Health is seeking an Experienced Clinical Research Associate to support sponsor-dedicated monitoring across clinical sites in the United States. The CRA will perform site qualification, initiation, monitoring, and close-out visits, ensuring GCP/ICH compliance and data integrity.

You will review informed consent, manage IP handling, ISF/TMF reconciliation, and support site staff training. Up to 75% travel, with opportunities for remote work in appropriate circumstances.