Clinical Research Associate (CRA) All Levels - West Coast

Evestia Clinical•Washington, MA

6d•Hybrid

About The Position

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.

Requirements

Degree in life sciences, nursing, pharmacy, or a related field; equivalent education and clinical research experience may be considered
Previous experience in clinical research, clinical operations, healthcare, or a related field is preferred; experience requirements will vary by level
For experienced CRA candidates, previous independent monitoring experience and the ability to perform applicable site visit types
Working knowledge of Good Clinical Practice (GCP), clinical trial regulations, and research ethics
Understanding of medical terminology, human physiology, and clinical trial processes
Strong written, verbal, and presentation skills
Proficiency with information technology and clinical trial systems
Excellent customer service, communication, and relationship-building skills
Demonstrated flexibility, adaptability, and attention to detail
Ability to work effectively in a team environment and independently as needed
Organizational and time management skills, with the ability to prioritize tasks and meet project timelines
Ability to travel nationally and internationally as required
Ideally based on the West Coast or within reasonable access to West Coast clinical trial sites

Responsibilities

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, escalate, 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