Remote Clinical Research Associate | Site Monitoring Pro

Syneos Health, Inc.; Virginia Beach (VA); On-site; USD 90,000 - 120,000; Full time

Job summary

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to support site qualification, initiation, monitoring, and close-out across the United States, with remote and on-site flexibility.

You will verify informed consent, ensure data integrity, and coordinate with sponsor teams to advance clinical trials. The role requires strong communication skills, GCP knowledge, and the ability to travel up to 75% in the US.

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.
• Must demonstrate good computer skills and be able to embrace new technologies.
• Excellent communication, presentation and interpersonal skills.
• 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) in compliance with ICH-GCP and GPP and study protocol.
• Verifies informed consent procedures and protects subject confidentiality and data integrity.
• Conducts source document review, data verification, query resolution and CRF data entry oversight across sites.
• Manages IP inventory, storage, labeling, and accountability and monitors IP-related risks.
• Maintains ISF/TMF accuracy and ensures archiving per local guidelines and regulations.
• Documents activities, supports recruitment/retention strategies, and tracks action items to resolution.
• Collaborates with sponsor teams, trains site staff, and participates in investigator meetings and project reviews.

Education

Bachelor's degree

RN

Job description

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to support site qualification, initiation, monitoring, and close-out across the United States, with remote and on-site flexibility.

You will verify informed consent, ensure data integrity, and coordinate with sponsor teams to advance clinical trials. The role requires strong communication skills, GCP knowledge, and the ability to travel up to 75% in the US.