Remote CRA II: Clinical Monitoring & Site Leadership

Syneos Health, Inc.; Rhode Island; Hybrid; USD 85,000 - 110,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits (medical, dental, and/

401k company match

Employee Stock Purchase Plan

Bonus eligibility

Flexible PTO and sick time

Job summary

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate (CRA) to support regionally aligned monitoring across the United States. The role involves site qualification, initiation, interim monitoring, and close-out visits, performed on-site or remotely, ensuring ICH-GCP compliance and data integrity.

You will collaborate with cross-functional teams, manage site relationships, and contribute to quality and regulatory readiness while supporting patient safety and study timelines.

Qualifications

• Bachelor's degree or RN required.
• Knowledge of Good Clinical Practice/ICH guidelines and regulatory requirements.
• Strong computer and data management skills are essential.
• Excellent communication and interpersonal skills; ability to travel up to 75%.

Responsibilities

• Performs site qualification, initiation, monitoring and close-out visits (on-site or remote) ensuring ICH-GCP compliance and protocol adherence.
• Verifies informed consent and protects subject confidentiality; assesses safety and data integrity at sites.
• Conducts Source Document Review and data query resolution; ensures accurate CRF data entry and IP handling per protocol.
• Maintains ISF/TMF accuracy; supports site training and archival requirements.
• Documents activities with letters, trip reports, and logs; supports recruitment and retention strategies.
• Acts as a liaison with site personnel; participates in investigator meetings and sponsor visits.

Skills

GCP knowledge

Computer skills

Excellent communication

Travel up to 75%

Education

Bachelor's degree or RN

Job description

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate (CRA) to support regionally aligned monitoring across the United States. The role involves site qualification, initiation, interim monitoring, and close-out visits, performed on-site or remotely, ensuring ICH-GCP compliance and data integrity.

You will collaborate with cross-functional teams, manage site relationships, and contribute to quality and regulatory readiness while supporting patient safety and study timelines.