Senior Clinical Research Associate - CNS/Oncology - West Coast

What You Will Do Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects. This role involves all stages of the clinical study, including: Identifying potential sites to participate in the research effort. Performing study start‑up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets. Training sites to collect data properly and report any potential safety‑related events. Managing the site’s activities during study maintenance. Closing down research activities at the sites once the study has concluded. Conducting study initiation visits (SIVs). Ensuring compliance with obtaining informed consent, reporting potential safety‑related events, and adhering to all applicable regulatory requirements. What You Will Bring to the Role Excellent interpersonal, oral, and written communication skills in English. Superior organizational skills with attention to detail. Ability to work with little or no supervision. Proficiency in Microsoft Office, CTMS, and EDC systems. Your Experience 5+ years of experience as a Clinical Research Associate. 4‑year university degree or Nursing degree. Experience in CNS and Oncology required. Candidate must reside on the West Coast. Willingness to travel regionally required. Equal Employment Opportunity We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law. #J-18808-Ljbffr Worldwide Clinical Trials Holdings, Inc.