
10,000+ employees
Founded 1996
🏥 Healthcare
💼 Consulting
🏭 Manufacturing
Healthcare • Consulting • Manufacturing
Novartis is an innovative medicines company dedicated to reimagining medicine to improve and extend people’s lives. With a presence in over 250 million patients worldwide, Novartis focuses on harnessing scientific breakthroughs to develop transformative, high-value treatments in areas such as cardiovascular, renal and metabolic diseases, immunology, neuroscience, and oncology. The company is committed to diversity, equity, and inclusion, and aims to create a positive impact through societal contributions and environmental sustainability efforts. Furthermore, Novartis engages in research collaborations and embraces modern technology platforms to advance their research and development capabilities, making them a leader in the global healthcare industry.
🔥 16 hours ago
🏄 California, Nevada, +2 more states – Remote
💵 $108.5k - $201.5k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
👻 Ghost score 0%
Where this job comes from
Posted on Novartis's careers page, not through a job board
First seen by Remote Rocketship 16 hours ago
Still open on Novartis's site. Checked 49 minutes ago.

10,000+ employees
Founded 1996
🏥 Healthcare
💼 Consulting
🏭 Manufacturing
Healthcare • Consulting • Manufacturing
Novartis is an innovative medicines company dedicated to reimagining medicine to improve and extend people’s lives. With a presence in over 250 million patients worldwide, Novartis focuses on harnessing scientific breakthroughs to develop transformative, high-value treatments in areas such as cardiovascular, renal and metabolic diseases, immunology, neuroscience, and oncology. The company is committed to diversity, equity, and inclusion, and aims to create a positive impact through societal contributions and environmental sustainability efforts. Furthermore, Novartis engages in research collaborations and embraces modern technology platforms to advance their research and development capabilities, making them a leader in the global healthcare industry.
• Manage trusted site relationships and perform on-site and remote monitoring activities for Phase I–IV clinical trials • Serve as the primary site manager and first point of contact between site staff and Novartis • Support collaboration, milestones, and deliverables as a frontline liaison • Monitor according to legislation, ICH/GCP, Novartis standards, monitoring plans, and procedures • Conduct site initiation visits and deliver ongoing training for site personnel • Perform continuous on-site and remote monitoring for protocol, GCP, regulatory, process compliance, data integrity, and patient safety • Facilitate preparation and collection of site- and country-level documents • Identify risks, resolve issues, and escalate concerns as needed • Collaborate with cross-functional teams to drive efficient study execution and process improvements • Deliver timely, high-quality, robust, reliable site data supporting Trial Monitoring goals • Partner with the SSU CRA for seamless transition of site responsibility • Act as a subject matter expert across study activities when required • Support audit and inspection readiness activities and corrective-action implementation • Drive clinical trials forward at the site level with patients at the center
• Minimum of 3 years’ experience in site monitoring • BS/BA degree in a scientific, healthcare, or related field • Excellent knowledge of the drug development process, specifically clinical trial/research • Knowledge 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 skills • Strong communication and presentation skills, oral and written • Fluent in both written and spoken English • Fully valid and unrestricted driver’s license • Ability to be located in the western region of the United States near a major airport, preferably in California, Washington State, Oregon, or Nevada • Ability to travel 80%
• Performance-based cash incentive • Eligibility to be considered for annual equity awards, depending on the level of the role • Health benefits • Life benefits • Disability benefits • 401(k) with company contribution and match • Vacation • Personal days • Holidays • Other leaves • Reasonable accommodations for qualified individuals with disabilities
Apply NowImprove your chances of getting an interview by checking your resume score before you apply.
🔥 16 hours ago
Associate Director overseeing pharmacovigilance operations, vendors, compliance, and safety reporting. Supporting Liquidia’s pulmonary hypertension therapies across clinical trials and marketed products.
🔥 17 hours ago
Senior Clinical Study Manager overseeing clinical trials and health-system pilots for Viz.ai’s AI-powered healthcare platform. Managing sponsors, sites, timelines, enrollment, data quality, and regulatory compliance.
🇺🇸 United States – Remote
💵 $129k - $145k / year
💰 Venture Round - Viz on 2023-12
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
🔥 19 hours ago
Senior Clinical Trial Leader overseeing global oncology trials for Alentis Therapeutics, a clinical-stage biotechnology company developing antibody-drug conjugates and CLDN1-targeting antibodies.
🔥 20 hours ago
Clinical Research Manager coordinating sponsor-dedicated clinical project plans, teams, budgets, and timelines. Supporting ICON’s global development of treatments through high-quality project delivery.
🕒 Yesterday
Senior pharmacovigilance scientist supporting Belite Bio’s retinal disease drug development. Managing safety cases, signal detection, regulatory reporting, and global compliance.
🇺🇸 United States – Remote
💵 $148k - $160k / year
🔥 Funding within the last year
💰 $402M Post-IPO Equity on 2025-12
⏰ Full Time
🟠 Senior
🧪 Clinical Research