Senior CRA: Trial Coordination & Site Oversight

Artiva Biotherapeutics Inc.; San Diego (CA); On-site; USD 110,000 - 135,000; Full time

Benefits offered by this job

Medical, Dental, Vision

401(k) Retirement Plan

Paid Time Off

Year-end holidays

Bonus.ly recognition program

Job summary

Artiva Biotherapeutics Inc. in San Diego seeks a Sr. Clinical Research Associate to support moderately complex clinical trial activities, ensuring GCP compliance and site start-up through close-out.

You will join a collaborative team, coordinate site activities, manage essential documents, review monitoring visits, and help drive vendor oversight with a focus on data quality and patient safety.

Qualifications

• Bachelor's degree or higher.
• 3+ years in Pharma/Biotech/CRO with at least 1 year site experience.
• GCP regulations and SOP knowledge.
• Proficiency with Word, Excel, and PowerPoint.

Responsibilities

• Organizes study team activities with agendas and minutes.
• Manages Site Essential Documents across start-up, maintenance, and close-out.
• Prepares study documents (consents, site instructions, MOA, pharmacy binder).
• Tracks essential documents in appropriate systems.
• Monitors patient status at investigative sites and maintains status databases.
• Reviews trip reports, data queries, site visit metrics, and overall site performance.
• Performs routine monitoring at limited sites; participates in site initiation and close-out visits.
• Ensures data quality and resolves eligibility/protocol deviations.
• Assist in investigator/vendor meetings and feasibility assessments.

Skills

Communication skills

Travel readiness

Site monitoring experience

GCP knowledge

SOP proficiency

Documentation detail

Education

Bachelor's degree or higher

Tools

MS Office

SQL/DB basics

Job description

Artiva Biotherapeutics Inc. in San Diego seeks a Sr. Clinical Research Associate to support moderately complex clinical trial activities, ensuring GCP compliance and site start-up through close-out.

You will join a collaborative team, coordinate site activities, manage essential documents, review monitoring visits, and help drive vendor oversight with a focus on data quality and patient safety.