Senior Clinical Research Associate

#LI-RemoteInternal job title: Sr CRAJob Description SummaryThis is a field-based and remote opportunity in an assigned geography. Novartis is unable to offer relocation support for this role. Please only apply if this location is accessible for you. This position must be located in the western region of the United States near major airport (preferably in California, Washington State, Oregon, Nevada). Drive clinical trials forward where it matters most - at the site level and with patients at the center. As a Senior CRA at Novartis, you will manage trusted site relationships and perform on-site and remote monitoring activities to support the initiation, conduct, and timely completion of Phase I – IV trials in compliance with International Council for Harmonization / Good Clinical Practices (ICH/GCP), local regulations, Standard Operating Procedures (SOPs), and monitoring procedures. Serving as a key point of contact for investigational sites, you will proactively manage site performance, recruitment, quality, risks, and issue resolution to ensure sustainable trial execution and high-quality data delivery. Assigned to complex trials and/or less experienced sites, you may also act as a Subject Matter Expert, support audit and inspection readiness activities, ensure timely implementation of corrective actions, and collaborate with local and global cross-functional teams to drive process improvements that help bring innovative therapies to patients faster. This position will require 80% travel.

Job descriptionKey responsibilities:Primary site manager and first point of contact between site staff and NovartisFrontline liaison supporting collaboration, milestones, and deliverablesMonitor according to legislation, ICH/GCP, and Novartis standardsManage assigned sites/networks conducting Phase I–IV protocols according to monitoring plans and Novartis proceduresConduct site initiation visits and deliver ongoing training for site personnelContinuous on-site/remote monitoring; protocol, GCP, regulatory and process compliance; data integrity and patient safetyFacilitate preparation and collection of site- and country-level documentsIdentify risks, resolve issues, and escalate concerns as neededCollaborate with cross-functional teams to drive efficient study executionDeliver timely, high-quality, robust, reliable site data supporting Trial Monitoring goalsPartner with SSU CRA for seamless transition of site responsibilityAct as a subject matter expert across study activities when required Essential Requirements:Minimum of 3 years’ experience in site monitoringBS/BA degree. Scientific, Healthcare or other related field.Excellent knowledge of the drug development process specifically clinical trial/researchKnowledge of international standards (GCP/ICH, FDA, EMEA)Ability to manage multiple priorities and manage time efficiently.Excellent Site management capabilities with demonstrated negotiating and problem-solving skillsStrong communicator and presentation skills (oral and written)Fluent in both written and spoken English Desirable Requirements:Cardiology, Oncology, CART, RLT & Immunology experience a plus! The salary for this position is expected to range between $108,500 and $201,500 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a  variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. To learn more about the culture, rewards and benefits we offer our people click here.Driving and air travel are an Essential Function of this Role: Meaning it is fundamental to the purpose of this job and cannot be eliminated. Because driving is an essential function of the role, you must have a fully valid and unrestricted driver’s license to be qualified for this role. The company provides reasonable accommodations for otherwise qualified individuals with medical restrictions if an accommodation can be provided without eliminating the essential function of driving. COVID-19 Vaccine Policy (customer-facing roles only): While Novartis does not require vaccination for COVID-19 or proof of a recent negative test result for COVID-19 at this time, employees working in customer-facing roles must adhere to and comply with customers’ (such as hospitals, physician offices, etc.) credentialing guidelines, which may require vaccination. As required by applicable law, Novartis will consider requests for reasonable accommodation for those unable to be vaccinated. This requirement is subject to applicable state and local laws and may not be applicable to employees working in certain jurisdictions. Please send accommodation requests to Eh.occupationalhealth@novartis.com.