Remote Sponsor‑Dedicated CRA II

Syneos Health, Inc.; Washington; Hybrid; USD 90,000 - 130,000; Full time

Job summary

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate - Sponsor Dedicated. The role involves remote monitoring across sites, ensuring ICH-GCP compliance, and providing site-level guidance to maintain data integrity.

You will coordinate with sponsor teams and manage trial activities, while traveling up to 75% as needed. Required are a bachelor’s degree or RN, knowledge of GCP/ICH guidelines, strong communication skills, and the ability to adapt to evolving study demands.

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) ensuring regulatory, ICH-GCP and/or GPP compliance.
• Verifies informed consent process and protects subject/patient confidentiality.
• Reviews ISF/TMF, conducts source data review, and ensures accurate CRF data entry and timely query resolution.
• Manages IP inventory, dispatch, labeling, and storage per protocol.
• Maintains training and ensures site personnel compliance with applicable requirements.

Skills

Excellent communication

Presentation skills

Interpersonal skills

Knowledge of GCP/ICH Guidelines

Computer skills

Travel ability 75%

Education

Bachelor’s degree

RN (optional)

Job description

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate - Sponsor Dedicated. The role involves remote monitoring across sites, ensuring ICH-GCP compliance, and providing site-level guidance to maintain data integrity.

You will coordinate with sponsor teams and manage trial activities, while traveling up to 75% as needed. Required are a bachelor’s degree or RN, knowledge of GCP/ICH guidelines, strong communication skills, and the ability to adapt to evolving study demands.