Remote Clinical Research Associate - Site Monitoring Pro

Syneos Health, Inc.; California; Sur place; USD 70 000 - 100 000; Plein temps

Avantages offerts par ce poste

Company car / car allowance

Health benefits (Medical, Dental, Vis

401k with company match

Employee Stock Purchase Plan

Paid time off (PTO) and sick time

Résumé du poste

Syneos Health is seeking an Experienced Clinical Research Associate to join our regionally aligned team across the US. In this CRA II role, you will perform site qualification, initiation, interim monitoring, and close-out visits, on-site or remotely, while ensuring ICH-GCP compliance and protocol adherence.

You will verify informed consent, monitor data quality, manage queries, and support site staff throughout the trial lifecycle.

Qualifications

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

Responsabilités

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (on-site or remote) ensuring regulatory, ICH-GCP and protocol compliance.
• Verifies informed consent and protects subject confidentiality; assesses factors affecting safety and data integrity.
• Reviews ISF/TMF, coordinates site training, and supports recruitment and data query resolution.
• Maintains knowledge of GCP guidelines and SOPs; may liaise with sponsor meetings and audit readiness.

Connaissances

GCP/ICH

Communication

Travel

Formation

Bachelor's degree or RN

Description du poste

Syneos Health is seeking an Experienced Clinical Research Associate to join our regionally aligned team across the US. In this CRA II role, you will perform site qualification, initiation, interim monitoring, and close-out visits, on-site or remotely, while ensuring ICH-GCP compliance and protocol adherence.

You will verify informed consent, monitor data quality, manage queries, and support site staff throughout the trial lifecycle.