Senior Oncology CRA - Remote Site Monitoring

1001 Syneos Health, LLC; Oregon; Hybrid; USD 85,000 - 120,000; Full time

Benefits offered by this job

Health benefits (Medical, Dental, VIsn

Company 401k match

Commission/bonus eligibility

PTO and sick time

Job summary

Syneos Health is seeking a CRA II/Sr CRA - Oncology (Homebased US only) to monitor clinical sites, ensure compliance with ICH-GCP and protocol requirements, and support subject safety and data integrity. The role involves significant travel (up to 75%), collaboration with cross-functional teams, and potential training of junior staff.

The candidate should hold a Bachelor’s degree or RN, possess strong communication skills, and be proficient with clinical data systems and regulatory guidance.

Qualifications

• Bachelor’s degree or RN and relevant regulatory knowledge.
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Excellent 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, site initiation, interim monitoring, site management and close-out visits (on-site or remote).
• Evaluates site performance and recommends site-specific actions; communicates issues to project team.
• Maintains knowledge of ICH/GCP Guidelines and applicable regulations; adheres to SOPs.
• Verifies informed consent and protects confidentiality of subjects/patients.
• Manages data capture and query resolution; ensures protocol adherence.
• Supports IP inventory, reconciliation; ensures proper labeling/importing per protocol.
• Ensures site is trained and compliant with applicable requirements; attends Investigator Meetings.
• May train junior staff and liaise with sponsor and country staff.

Skills

Communication skills

Travel flexibility

GCP knowledge

Education

Bachelor’s degree or RN

Job description

Syneos Health is seeking a CRA II/Sr CRA - Oncology (Homebased US only) to monitor clinical sites, ensure compliance with ICH-GCP and protocol requirements, and support subject safety and data integrity. The role involves significant travel (up to 75%), collaboration with cross-functional teams, and potential training of junior staff.

The candidate should hold a Bachelor’s degree or RN, possess strong communication skills, and be proficient with clinical data systems and regulatory guidance.