Senior Clinical Research Associate - Remote & Site Mgmt

Syneos Health/ inVentiv Health Commercial LLC; Chicago (IL); On-site; USD 85,000 - 120,000; Full time

Benefits offered by this job

Company car/allowance

Health benefits

401(k) match

Employee stock purchase plan

Paid time off

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate dedicated to sponsor-driven monitoring. The role involves site qualification, initiation, monitoring, and close-out activities, with the flexibility of remote activities where appropriate.

The ideal candidate holds a Bachelor's degree or RN and possesses strong GCP knowledge, data integrity focus, and exceptional communication skills. Travel up to 75% is required, with opportunities across US sites and sponsor collaborations.

Qualifications

• Bachelor's degree or RN in a related field or equivalent.
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Good computer skills and ability to adapt to new technologies.
• Excellent communication, presentation and interpersonal skills.
• Ability to travel up to 75% on a regular basis.

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management and close-out visits (on-site or remote) ensuring regulatory, ICH‑GCP and/ or GPP compliance.
• Verifies informed consent processes and protects subject confidentiality and data integrity.
• Reviews ISF and TMF, guides site staff on query resolution, and ensures timely data capture and ISF/TMF alignment.
• Manages IP inventory, storage, labeling, and distribution per protocol; ensures proper handling of blinded or randomized information.
• Prepares for Investigator Meetings and sponsor visits; participates in global project meetings and trainings.

Skills

Excellent communication

Willingness to travel

Regulatory knowledge

Education

Bachelor's degree or RN

Job description

Syneos Health is seeking an Experienced Clinical Research Associate dedicated to sponsor-driven monitoring. The role involves site qualification, initiation, monitoring, and close-out activities, with the flexibility of remote activities where appropriate.

The ideal candidate holds a Bachelor's degree or RN and possesses strong GCP knowledge, data integrity focus, and exceptional communication skills. Travel up to 75% is required, with opportunities across US sites and sponsor collaborations.