Senior Clinical Trials CRA — Remote Site Lead

Parexel; Helena (MT); On-site; USD 75,000 - 100,000; Full time

Job summary

Parexel is seeking a Senior Clinical Research Associate I (Sr. CRA) to oversee site management and monitoring across assigned trials. You will work to ensure patient safety, data quality, and regulatory compliance in collaboration with the SCP and study team.

You will travel frequently (60-80% expected), coach site staff on protocol requirements, and support site initiation, conduct and close-out activities while maintaining strong sponsor relationships and quality standards.

Qualifications

• Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local regulations.
• Minimum 3 years of site monitoring experience in clinical research.
• Oncology or related therapeutic area experience preferred.

Responsibilities

• Ensure proper conduct of trials per SMP, laws, GCP and client standards.
• Manage site activation through database lock with timely, quality deliverables.
• Be primary contact for investigator sites and coordinate with SCP.
• Monitor AE/SAE reporting and site communications; ensure documentation integrity.

Skills

ICH-GCP knowledge

FDA regulations

Oncology monitoring

Site management

Communication skills

Travel willingness

English fluency

Education

Bachelor's degree in life sciences

Job description

Parexel is seeking a Senior Clinical Research Associate I (Sr. CRA) to oversee site management and monitoring across assigned trials. You will work to ensure patient safety, data quality, and regulatory compliance in collaboration with the SCP and study team.

You will travel frequently (60-80% expected), coach site staff on protocol requirements, and support site initiation, conduct and close-out activities while maintaining strong sponsor relationships and quality standards.