Home-Based CRA II: Oncology & Ophthalmology Trials

Syneos Health/ inVentiv Health Commercial LLC; Illinois; On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Company car/allowance

Health benefits

401k match

Stock Purchase Plan

Job summary

Syneos Health is seeking a CRA II for Oncology and Ophthalmology, home-based in the Midwestern region. The role focuses on site qualification, monitoring and management while ensuring compliance with ICH-GCP and regulatory requirements.

You will support source data verification, consent processes, and data integrity across an array of sites. Responsibilities include coordinating with site staff and sponsor teams, conducting site visits remotely or on-site, and managing trial documentation.

Qualifications

• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Excellent communication, presentation and interpersonal skills.
• Must demonstrate good computer skills and be able to embrace new technologies.
• US ONLY: deployment to sites requiring access to facilities; comply with privacy notice.
• Ability to manage 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) with regulatory and protocol compliance.
• Verifies informed consent and protects patient confidentiality while assessing safety and data integrity.
• Reviews site processes, conducts source data review, and ensures accurate data entry and query resolution.
• Manages IP inventory and ensures proper labeling, handling, and release of IP per protocol.
• Maintains ISF/TMF alignment and supports recruitment, retention and tracking observations.
• Prepares for investigator meetings and participates in sponsor/region training and audits.

Skills

Excellent communication

Good computer skills

Willingness to travel up to 75%

Education

Bachelor's degree or RN

Job description

Syneos Health is seeking a CRA II for Oncology and Ophthalmology, home-based in the Midwestern region. The role focuses on site qualification, monitoring and management while ensuring compliance with ICH-GCP and regulatory requirements.

You will support source data verification, consent processes, and data integrity across an array of sites. Responsibilities include coordinating with site staff and sponsor teams, conducting site visits remotely or on-site, and managing trial documentation.