Job Description

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. We are hiring a Clinical Research Coordinator (CRC) to support daily activities of early phase oncology clinical trials. Key responsibilities include patient interaction, data collection, and maintaining compliance with Good Clinical Practice (GCP). The CRC will manage multiple protocols, oversee protocol execution, and ensure timely, accurate conduct. Essential Responsibilities Communicate regularly with Study Sponsor’s, CRO’s, staff, etc. regarding protocol status. Monitor day‑to‑day conduct of studies in accordance with protocols, SOPs, and GCP. Create and review study documents to assure protocol compliance. Maintain files using standardized labeling and filing procedures. Implement initial protocol and amendments, and train staff involved in patient care. Maintain an up‑to‑date contact list. Assist with patient screening and eligibility determination. Facilitate the informed consent process. Prepare and manage source documents according to SOPs. Identify protocol deviations and work with leadership to implement corrective actions. Assist data coordinator team with case report form completion and query resolution. Work with Principal Investigator to complete and submit Serious Adverse Event reports. Perform protocol‑specific closeout activities jointly with the data coordinator. Provide documentation for all deviations, protocol or SOP‑related. Ensure all team members understand and adhere to assigned protocols. Required Education and Experience High School Diploma or GED. 2 years of clinical research experience. Basic understanding of oncology clinical trials, particularly Phase1 studies. Strong attention to detail and accuracy in data collection and documentation. Ability to manage multiple tasks and meet deadlines in a fast‑paced environment. Excellent organizational and time‑management skills. Strong written and verbal communication skills. Professional interaction with patients, study staff, and external stakeholders. Working knowledge of GCP and regulatory requirements. Proficiency in Microsoft Office Suite and clinical trial management software. Preferred Education and Experience Experience working in an oncology setting. Physical & Travel Requirements Sitting for extended periods of time. Prolonged use of computer, keyboard, and mouse. Benefits and Perks Competitive hourly base salary of $43–$53 per hour. Bidirectional work schedule: Monday–Friday 8:00 am–5:00 pm. Location: START LosAngeles, CA. 401(k) retirement savings plan with employer match. Eligibility for an annual performance bonus. Generous paid time off and paid holidays. Comprehensive medical, dental, and vision coverage. Optional insurance options, including company‑paid life and disability insurance. Employee Assistance Program (EAP) providing confidential support. Flexible FSA and HSA plans. Supportive environment valuing balance, wellbeing, and flexibility. We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. #J-18808-Ljbffr

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