Full-time jobs in San Diego, CA

About the role

This position will be responsible for managing the biomarker operation of Artiva’s clinical studies by coordinating sample-related operations with Clinical Operations, contract executions, and communication between the Translational Science group with external contract research organizations (CRO) and internal lab personnel. The successful candidate will have strong communication and project management skills.

What you'll bring

• Understanding and experience with drug development and clinical trial process
• Must thrive working in a fast-paced innovative environment while remaining flexible, proactive, and efficient.
• Excellent communication, project management and interpersonal skills.
• Able to develop important relationships with key internal stakeholders and external entities.
• Bachelor’s or Master's degree in biology, immunology, or related fields and/or project management experience is required with a minimum of 6 - 8 years’ experience within the biotechnology or pharmaceutical industry
• Demonstrated experience of managing biomarker sample operation of clinical trials, working with CROs to execute biomarker study plan.
• Excellent communication skills, verbal and written
• Communication skills
• Time Management
• Risk Management
• Operations Management
• Finance

Benefits