Clinical Research Associate; CRA; West Coast

EPIC.
Evestia Clinical is a biotech-focused global CRO delivering authentic expertise and personalized support. We partner with clients to provide expert guidance through complex clinical trials in specialized areas, including Rare Disease, Oncology, Neurology, and Immunology. Here, you become a vital part of a global team delivering life-changing impact through clinical excellence.

We are building something
EPIC.
Evestia Clinical is a biotech-focused global CRO delivering authentic expertise and personalized support. We partner with clients to provide expert guidance through complex clinical trials in specialized areas, including Rare Disease, Oncology, Neurology, and Immunology. Here, you become a vital part of a global team delivering life-changing impact through clinical excellence.
Our foundation is built on principles that define our identity.
Innovation drives us to seek new solutions, while Excellence ensures high standards in every project. This is balanced by genuine Care
, fostering a supportive culture for both our patients and our people. Above all, we champion Partnership
, believing that working together—with trust and flexibility—is the key to our collective success.
Our approach is agile and personalized, empowering you to find creative solutions. We offer a welcoming culture that values belonging, ensuring you have the environment needed to thrive and grow. If you are ready to change lives worldwide, join our team.

Evestia Clinical is looking for Clinical Research Associates at all levels to join our team on the West Coast. In this role, you will help ensure that the rights, safety, and well‑being of clinical trial participants are protected and that the clinical data collected are accurate, complete, and verifiable according to source documents and applicable requirements.
Depending on experience, you may contribute to clinical trials from study start‑up and site initiation through routine monitoring, close‑out, and study completion. This is an opportunity to develop your career within a collaborative, global clinical research environment focused on quality, compliance, and meaningful patient impact.

• Perform site management and monitoring activities appropriate to your level of experience, including site qualification, initiation, interim monitoring, and close‑out visits
• Participate in clinical trials from development and planning through study closure
• Ensure assigned clinical trial sites comply with the study protocol, applicable regulations, ICH/GCP, and Evestia Clinical or sponsor SOPs
• Review source documentation and clinical data to assess accuracy, completeness, and consistency
• Monitor participant safety, informed consent processes, investigational product accountability, and protocol compliance
• Identify, document, elevate, and support the resolution of issues, including protocol deviations and data queries
• Maintain key performance metrics in accordance with company standards, project requirements, and established timelines
• Prepare monitoring reports and other required study documentation accurately and within expected timelines
• Work collaboratively with Clinical Team Leads, Project Managers, sponsors, investigators, site personnel, and cross‑functional project teams
• Build and maintain effective relationships with clinical research sites and study stakeholders
• Complete required administrative activities, including expense and time reporting, within company guidelines
• For more experienced candidates, provide mentoring, guidance, and subject matter support to less experienced team members
• Perform any other duties as assigned

• Degree in life sciences, nursing, pharmacy, or a related field; equivalent education…