Remote Senior Clinical Research Associate – Sponsor Dedicated

Syneos Health, Inc.; Northern (KY); Hybrid; USD 60,000 - 90,000; Full time

Benefits offered by this job

Company car/Car allowance

Health benefits

401k match

Stock Purchase Plan

Flexible PTO & sick time

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate for sponsor-dedicated work. The role supports site qualification, initiation, monitoring, and close-out visits, with remote and on-site options across the USA. You will verify informed consent, review source documents, and manage data quality and IP handling while ensuring compliance with ICH-GCP and SOPs.

The position requires a Bachelor’s degree or RN, strong communication skills, and the ability to travel up to 75%.

Qualifications

• Bachelor’s degree or RN in related field; equivalent combination of education and experience may be considered.
• Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements.
• Excellent communication, presentation and interpersonal skills.
• Ability to manage travel up to 75% regularly.
• U.S. work eligibility and compliance with site access requirements.

Responsibilities

• Performs site qualification, initiation, monitoring, and close-out visits (on-site or remote) ensuring regulatory and protocol compliance.
• Verifies informed consent and protects subject confidentiality.
• Conducts source document review and CRF data accuracy checks; drives query resolution.
• Manages IP inventory, labeling, and handling per protocol; ensures proper archiving.
• Maintains ISF/TMF accuracy and auditors readiness; coordinates with site staff.

Skills

Communication skills

GCP knowledge

Computer skills

Travel readiness

Regulatory knowledge

Education

Bachelor's degree or RN in related field

Job description

Syneos Health is seeking an Experienced Clinical Research Associate for sponsor-dedicated work. The role supports site qualification, initiation, monitoring, and close-out visits, with remote and on-site options across the USA. You will verify informed consent, review source documents, and manage data quality and IP handling while ensuring compliance with ICH-GCP and SOPs.

The position requires a Bachelor’s degree or RN, strong communication skills, and the ability to travel up to 75%.