Job Summary
The Senior Clinical Research Associate (CRA) plays a pivotal role in the management and oversight of moderately complex clinical studies. Working within Artiva, a publicly traded biotechnology firm based in San Diego, California, the CRA will contribute to advancing clinical trials for various conditions, enhancing the company’s innovative research initiatives.
Responsibilities
- Assist in the planning and implementation of clinical trial protocols.
- Monitor site activities to ensure compliance with regulatory requirements.
- Facilitate communication between various stakeholders involved in clinical trials.
- Support the collection and management of clinical data.
- Evaluate and address site performance issues and implement corrective actions as necessary.
Qualifications
- Proven experience in clinical research, ideally in a similar clinical research associate role.
- Strong understanding of Good Clinical Practice (GCP) and regulatory guidelines.
- Excellent organizational and communication skills.
- Ability to work effectively both independently and as part of a team.
Artiva Biotherapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
