Regional Clinical Research Associate - Remote Monitoring

Syneos Health, Inc.; West Des Moines (IA); On-site; USD 70,000 - 110,000; Full time

Benefits offered by this job

Company car/Car allowance

Health benefits (Medical, Dental, and

401k match

Employee Stock Purchase Plan

Bonus eligibility

Paid time off

Job summary

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to join a regionally aligned team across the United States. The role focuses on monitoring sites, ensuring GCP compliance and data integrity, while collaborating with cross-functional teams to support trial delivery.

You will perform site initiation, monitoring visits, and close-out activities, either on-site or remotely, and support subject safety, data quality, and regulatory compliance throughout the study lifecycle.

Qualifications

• Bachelor's degree or RN in a related field or equivalent combination of education, training and experience.
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Excellent communication, presentation and interpersonal skills.

Responsibilities

• Performs site qualification, initiation, monitoring and close-out visits, on-site or remotely.
• Verifies informed consent processes and subject safety documentation.
• Ensures data accuracy in CRFs and supports query resolution within timelines.
• Maintains ISF and TMF accuracy and archiving requirements.
• Coordinates site training and supports site recruitment and retention strategies.

Skills

GCP knowledge

Excellent communication

Travel up to 75%

US work authorization

Education

Bachelor's degree or RN

Job description

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to join a regionally aligned team across the United States. The role focuses on monitoring sites, ensuring GCP compliance and data integrity, while collaborating with cross-functional teams to support trial delivery.

You will perform site initiation, monitoring visits, and close-out activities, either on-site or remotely, and support subject safety, data quality, and regulatory compliance throughout the study lifecycle.