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.
