Senior Clinical Research Associate – Global Trials

Syneos Health/ inVentiv Health Commercial LLC; Cheyenne (WY); On-site; USD 70,000 - 110,000; Full time

Benefits offered by this job

Company car or car allowance

Medical, Dental & Vision benefits

401k with company match

Employee Stock Purchase Plan

Commissions/bonus eligibility

Flexible paid time off & sick time

Paid sick time compliance

Job summary

Syneos Health seeks a Clinical Research Associate - Full-Service to monitor trials across sites, performing qualification, initiation, interim monitoring and close-out activities. You may work on-site or remotely, ensuring regulatory and ICH-GCP compliance.

Responsibilities include verifying informed consent, data integrity, ISF/TMF reconciliation, IP handling, and cross-functional collaboration. Travel up to 75% is required; a BA/BS or RN and strong communication are essential.

Qualifications

• Bachelors degree or RN with equivalent experience.
• Knowledge of Good Clinical Practice/ICH Guidelines and applicable regulatory requirements.
• Good computer skills and ability to embrace new technologies.
• Excellent communication, presentation and interpersonal skills.
• Ability to travel up to 75% regularly.

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management and close-out visits (on-site or remote) with regulatory and ICH-GCP compliance.
• Verifies informed consent process and protects patient confidentiality; assesses factors affecting safety and data integrity.
• Assesses site processes; conducts source data review and validates CRF data; drives closure of data queries.
• May perform IP inventory, validation, and labeling per protocol; ensures proper release and storage.
• Maintains ISF accuracy; reconciles with TMF and ensures archiving per local guidelines.
• Documents activities; supports recruitment, retention, and tracking; communicates with project team and sites.
• Manages scope, budgets, and timelines; adapts to changing priorities to meet objectives.
• Acts as liaison with study sites; ensures training and compliance across teams.
• Prepares for Investigator Meetings and attends meetings; contributes to audit readiness.

Skills

Excellent communication, presentation,

Willingness to travel up to 75%

Adaptability

Computer skills

Education

Bachelor's degree or RN in a related field or equivalent

Job description

Syneos Health seeks a Clinical Research Associate - Full-Service to monitor trials across sites, performing qualification, initiation, interim monitoring and close-out activities. You may work on-site or remotely, ensuring regulatory and ICH-GCP compliance.

Responsibilities include verifying informed consent, data integrity, ISF/TMF reconciliation, IP handling, and cross-functional collaboration. Travel up to 75% is required; a BA/BS or RN and strong communication are essential.