Senior Clinical Research Associate - CNS/Rare Disease - West Coast - Remote

What You Will Do Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects. Typically involved in all stages of the clinical study, including identifying potential sites, performing study start‑up activities, collecting regulatory documents, negotiating contracts and budgets, training sites to collect data properly, reporting safety‑related events, managing the site’s activities during study maintenance, and closing down research activities at the end of the study. Conduct study initiation visits (SIVs). While most site management is performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety‑related events, and adhering to all applicable regulatory requirements. What You Will Bring 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. Experience 5+ years of experience as a Clinical Research Associate. 4‑year university degree or Nursing degree. Experience in CNS/Neurology is required; Psychiatry and Rare Disease are strongly preferred. Candidates must reside on the West Coast. Willingness to travel regionally required. Equal Opportunity Employer Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed. 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.