Remote Regional Clinical Research Associate

Syneos Health, Inc.; Minneapolis (MN); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Company car/allowance

Health benefits

401k match

Stock purchase plan

Generous PTO

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate to join a regionally aligned team across the US. This role supports site qualification, initiation, monitoring, and close-out visits, with on-site or remote activities.

You will ensure ICH-GCP compliance, manage data and IP processes, and collaborate with sponsor teams. Travel up to 75% is required, with a focus on quality and patient safety.

Qualifications

• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Excellent communication, presentation and interpersonal skills.
• Must demonstrate good computer skills and be able to embrace new technologies.
• Ability to manage required travel of up to 75% on a regular basis.

Responsibilities

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (on-site or remotely).
• Verifies informed consent procedures and protects confidentiality of subjects.
• Reviews ISF/TMF, conducts source data verification and data capture; ensures IP handling per protocol.
• Maintains ISF and TMF alignment; trains site staff; supports recruitment, retention and tracking.
• Communicates with sponsor teams; prepares for Investigator Meetings and audit readiness.
• Ensures compliance with ICH/GCP and local regulations; supports project timelines and budgets.

Skills

GCP knowledge

Communication skills

Computer skills

Travel up to 75%

US work authorization

Education

Bachelor's degree or RN

Job description

Syneos Health is seeking an Experienced Clinical Research Associate to join a regionally aligned team across the US. This role supports site qualification, initiation, monitoring, and close-out visits, with on-site or remote activities.

You will ensure ICH-GCP compliance, manage data and IP processes, and collaborate with sponsor teams. Travel up to 75% is required, with a focus on quality and patient safety.