Clinical Research Coordinator

Clinical Research Coordinator (CRC)Location: Walnut Creek, California

Employment Type: Full-time, Monday–FridayA growing clinical research site is seeking a motivated and detail oriented Clinical Research Coordinator (CRC) to join its team in Walnut Creek, California.

This is an excellent opportunity for someone with hands on clinical research experience who is passionate about patient care, clinical trial delivery and contributing to the development of new treatments.The site conducts clinical trials across multiple therapeutic areas, including cardiology, metabolic and renal diseases, oncology, CNS, pulmonology and vaccines, offering exposure to a diverse range of clinical research studies.Key ResponsibilitiesExecute protocol specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG, etc.Coordinate clinical trials from study start up through completion, ensuring adherence to study protocols, SOPs, GCP guidelines and applicable FDA regulations.Recruit, screen and enrol eligible participants in accordance with study-specific inclusion and exclusion criteria.Conduct informed consent discussions and ensure all participant documentation is accurate and complete.Coordinate study visits, procedures, laboratory collections and follow up appointments.Collect, process and manage biological samples in accordance with study protocols.Maintain accurate source documentation, electronic case report forms (eCRFs) and regulatory study files.Monitor participant safety, document adverse events and escalate concerns to the Principal Investigator as appropriate.Liaise with Principal Investigators, Sub-Investigators, sponsors, CROs and other clinical research stakeholders.Support monitoring visits, audits and inspections, ensuring ongoing compliance and data quality.Provide a positive, professional and patient-focused experience throughout the clinical trial process.RequirementsPrevious experience as a Clinical Research Coordinator, Research Coordinator or in a similar clinical research role.Experience coordinating clinical trials and managing study activities in a clinical research site, hospital or comparable research setting.Working knowledge of ICH-GCP, FDA regulations and clinical trial protocols.Experience with informed consent, patient screening, study visits, source documentation and data entry.Strong organisational skills and the ability to manage multiple studies and competing priorities.Excellent communication and interpersonal skills, with a patient-centred approach.High attention to detail and a commitment to research quality, participant safety and regulatory compliance.What’s on OfferOpportunity to contribute to a diverse portfolio of clinical research studies.A collaborative, patient-focused working environment.Exposure to multiple therapeutic areas and clinical trial phases.Full-time, weekday working hours.Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, employee referral program, employee assistance program, life insurance, disability