Remote Clinical Research Associate - Global Trials Impact

Syneos Health, Inc.; Wyoming (MI); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Company car/allowance

Health benefits (medical, dental, and视

401k match

Employee stock purchase plan

Paid time off

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate to support regional monitoring across US sites. The role emphasizes ICH-GCP compliance, site qualification/initiation, and data integrity in real-world and late-phase studies.

Travel up to 75% is required; you’ll partner with investigators, manage site files, and ensure audit readiness while delivering high-quality clinical outcomes for patients and sponsors.

Qualifications

• Bachelor's degree or RN in a related field.
• Knowledge of Good Clinical Practice/ICH Guidelines.
• Excellent communication, presentation and interpersonal skills.
• Ability to travel up to 75%.

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management activities and close-out visits (on-site or remote) with regulatory, ICH-GCP and GPP compliance.
• Verifies informed consent processes and protects patient confidentiality; assesses factors affecting subject safety and data integrity.
• Per the CMP/SMP: assesses site processes, conducts Source Document Review, and ensures data entry accuracy in CRFs; supports query resolution.
• May perform IP inventory, labeling, and storage reviews per protocol; ensures IP is used per protocol.
• Reviews ISF and TMF, ensures archiving per guidelines; maintains audit readiness.
• Documents activities and supports recruitment, retention and data tracking; manages timelines and action items.
• Understands project scope, budgets, and timelines; coordinates site communications and travel readiness; may train junior staff.

Skills

Communication

Interpersonal skills

GCP/ICH knowledge

Computer literacy

Travel readiness

Education

Bachelor's degree or RN in related field

Job description

Syneos Health is seeking an Experienced Clinical Research Associate to support regional monitoring across US sites. The role emphasizes ICH-GCP compliance, site qualification/initiation, and data integrity in real-world and late-phase studies.

Travel up to 75% is required; you’ll partner with investigators, manage site files, and ensure audit readiness while delivering high-quality clinical outcomes for patients and sponsors.