Clinical Research Associate - Remote Monitoring & Site Management

Syneos Health, Inc.; Arizona; Remote; USD 70,000 - 110,000; Full time

Job summary

Syneos Health, Inc. seeks an Experienced Clinical Research Associate to work regionally across the United States. You will monitor sites, ensure regulatory compliance, and support trial conduct from initiation to close-out while collaborating with study teams.

The role requires strong knowledge of ICH-GCP, excellent communication, and the ability to travel up to 75%. You’ll interact with sites, manage documentation, and contribute to audit readiness in a dynamic, patient-focused environment.

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
• US ONLY: As part of your employment with Syneos Health, you may be deployed to Sites that require certain medical and other personal information to gain facility access. Further, a Site may ask you for additional information beyond that which Syneos Health has in its possession. You are required to comply with any such Site requests as a condition of your employment with Syneos Health.

Responsibilities

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.
• Verifies informed consent documentation and protects subject confidentiality while assessing safety and data integrity.
• Reviews ISF/TMF, trains site staff, and supports subject recruitment and data tracking.
• Manages IP inventory and ensures proper labelling, storage and release per protocol.
• Ensures site compliance with data capture requirements and conducts source data verification.

Skills

Excellent communication

Interpersonal skills

Good computer skills

Travel up to 75%

GCP/ICH knowledge

Education

Bachelor's degree or RN in related field

Job description

Syneos Health, Inc. seeks an Experienced Clinical Research Associate to work regionally across the United States. You will monitor sites, ensure regulatory compliance, and support trial conduct from initiation to close-out while collaborating with study teams.

The role requires strong knowledge of ICH-GCP, excellent communication, and the ability to travel up to 75%. You’ll interact with sites, manage documentation, and contribute to audit readiness in a dynamic, patient-focused environment.