Senior Field CRA - Remote Site Monitoring (West US)

Novartis AG

Sacramento (CA)

Remote

USD 109,000 - 202,000

Full time

8 days ago

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Benefits offered by this job

Health, life and disability benefits
401(k) with company match
Generous time off package

Job summary

Novartis AG is seeking a Senior Clinical Research Associate (Sr CRA) for a field-based, remote opportunity mainly in the western United States. The role requires 80% travel and focuses on monitoring Phase I–IV trials, ensuring data integrity, patient safety, and regulatory compliance.

You will manage site relationships, conduct ICH/GCP compliant monitoring, and collaborate with cross-functional teams to drive trial success.

Qualifications

  • Minimum 3 years’ experience in site monitoring.
  • BS/BA degree in Scientific, Healthcare or related field.
  • Strong knowledge of drug development, ICH/GCP and FDA/EMEA.
  • Excellent communication, time management and problem-solving skills.
  • Fluent English, both written and spoken.

Responsibilities

  • Serve as primary site manager and main point of contact for site staff and Novartis.
  • Monitor according to ICH/GCP, SOPs and regulatory requirements.
  • Conduct site initiation visits and provide ongoing training for site personnel.
  • Perform on-site and remote monitoring to ensure data quality and patient safety.
  • Collaborate with cross-functional teams to drive efficient study execution.
  • Identify risks, resolve issues, and escalate as needed.

Skills

Site monitoring
Communication
English fluency
Time management
Problem solving

Education

BS/BA in Scientific/Healthcare or related field

Tools

CTMS knowledge
EDC systems

Job description

Novartis AG is seeking a Senior Clinical Research Associate (Sr CRA) for a field-based, remote opportunity mainly in the western United States. The role requires 80% travel and focuses on monitoring Phase I–IV trials, ensuring data integrity, patient safety, and regulatory compliance.

You will manage site relationships, conduct ICH/GCP compliant monitoring, and collaborate with cross-functional teams to drive trial success.

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