Senior CRA – Onsite SF Site Monitoring (Contract)

BioPhase Inc.; San Francisco (CA); On-site; USD 110,000 - 150,000; Full time

Job summary

BioPhase Inc. in San Francisco seeks an experienced Senior Clinical Research Associate (CRA) to support trial execution and site monitoring.

You will independently manage monitoring activities and collaborate with internal teams, sites, vendors, and external partners to ensure studies are conducted efficiently and in compliance with regulations. The role requires a Bachelor’s degree in life sciences with 5+ years of clinical research experience, strong GCP/ICH knowledge, multi-site oversight,

Qualifications

• Bachelor’s degree in life sciences or related field; 5+ years of clinical research experience.
• Strong knowledge of GCP, ICH guidelines and regulatory requirements.
• Experience monitoring multiple sites with limited supervision.

Responsibilities

• Independently conduct site initiation, routine monitoring, and close-out activities.
• Oversee assigned sites, study timelines, deliverables, and issue resolution.
• Support study start-up and ongoing site/laboratory management activities.
• Maintain inspection-ready clinical documentation and TMF records.
• Collaborate with cross-functional teams and external partners throughout study execution.
• Support vendor oversight, data/reporting activities, and process improvements.
• Provide guidance and mentorship to less experienced clinical team members.

Skills

Independent monitoring

GCP/ICH knowledge

Multi-site oversight

Communication skills

Travel readiness

Education

Bachelor’s degree in life sciences or related field

Advanced degree or equivalent experience considered

Job description

BioPhase Inc. in San Francisco seeks an experienced Senior Clinical Research Associate (CRA) to support trial execution and site monitoring.

You will independently manage monitoring activities and collaborate with internal teams, sites, vendors, and external partners to ensure studies are conducted efficiently and in compliance with regulations. The role requires a Bachelor’s degree in life sciences with 5+ years of clinical research experience, strong GCP/ICH knowledge, multi-site oversight,