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Senior Clinical Research Associate

🔥 16 hours ago

🏄 California, Nevada, +2 more states – Remote

infoinfo

💵 $108.5k - $201.5k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

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.

Logo of Novartis

Novartis

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.

📋 Description

• 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

🎯 Requirements

• 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%

🏖️ Benefits

• 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

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