Field CRA – Cell Therapy Trials (Mid-Atlantic)

AstraZeneca plc; Oregon; Hybrid; USD 112,000 - 168,000; Full time

Job summary

AstraZeneca plc in the United States seeks a Clinical Research Associate (CRA) responsible for monitoring and site management across allocated sites, ensuring study delivery aligns with ICH-GCP and AstraZeneca SOPs. This field-based role favors candidates in the Mid-Atlantic region but requires nationwide travel as needed.

Key duties include site initiation, monitoring visits (on-site and remote), data review, regulatory maintenance, and collaboration with Local Study Teams to ensure timely

Qualifications

• 3+ years of CRA or similar clinical research experience.
• Excellent knowledge of ICH-GCP guidelines; GMP/GDP basics.
• Strong written and verbal communication skills.

Responsibilities

• Contributes to site selection and investigator qualification.
• Monitors studies per Monitoring Plans and ensures data accuracy.
• Maintains regulatory documentation and site training records.

Skills

CRA experience

ICH-GCP knowledge

Communication skills

Regulatory knowledge

Travel ability

Education

Bachelor's degree in Life Sciences

Tools

CTMS

eTMF

Regulatory submission tools

Job description

AstraZeneca plc in the United States seeks a Clinical Research Associate (CRA) responsible for monitoring and site management across allocated sites, ensuring study delivery aligns with ICH-GCP and AstraZeneca SOPs. This field-based role favors candidates in the Mid-Atlantic region but requires nationwide travel as needed.

Key duties include site initiation, monitoring visits (on-site and remote), data review, regulatory maintenance, and collaboration with Local Study Teams to ensure timely