Senior Clinical Research Associate: Global Trials

Syneos Health/ inVentiv Health Commercial LLC; Indianapolis (IN); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Company car/allowance

Health benefits

401k matching

Stock purchase plan

Bonus program

Flexible PTO

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate to perform site qualification, initiation, monitoring and close-out visits, either on-site or remotely. The role emphasizes regulatory compliance and data integrity across sponsor-delivered studies.

The candidate should hold a Bachelor's degree or RN and be proficient with ICH‑GCP guidelines, data capture systems and ability to travel up to 75% of the time. Our team supports global patient access and therapeutic delivery.

Qualifications

• Bachelor's degree or RN in a related field
• 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, initiation, monitoring, site management and close-out visits (on-site or remote) ensuring compliance with regulatory and ICH‑GCP requirements.
• Verifies informed consent process and protects patient confidentiality.
• Conducts source document review and data verification; drives query resolution to closure.
• May perform IP inventory, reconciliation and review storage and security as per protocol.
• Maintains ISF/TMF and supports audit readiness and site training requirements.
• Supports recruitment and data tracking; communicates with project team and sites to meet timelines.

Skills

Communication skills

Presentation skills

Interpersonal skills

Willingness to travel

GCP knowledge

Education

Bachelor's degree or RN

Job description

Syneos Health is seeking an Experienced Clinical Research Associate to perform site qualification, initiation, monitoring and close-out visits, either on-site or remotely. The role emphasizes regulatory compliance and data integrity across sponsor-delivered studies.

The candidate should hold a Bachelor's degree or RN and be proficient with ICH‑GCP guidelines, data capture systems and ability to travel up to 75% of the time. Our team supports global patient access and therapeutic delivery.