Senior Clinical Research Associate

🔥 24 minutes ago

🌾 Iowa, Kansas, +5 more states – Remote

🌾 Iowa – Remote 🌪️ Kansas – Remote 🌾 Nebraska – Remote 🌶️ New Mexico – Remote 🌪️ Oklahoma – Remote 🏰 Missouri – Remote 🤠 Texas – Remote

💵 $108.5k - $201.5k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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Novartis

WebsiteLinkedInAll Job Openings

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 • Support trial initiation, conduct, and timely completion in compliance with ICH/GCP, local regulations, SOPs, and monitoring procedures • 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 • Manage assigned sites and networks according to monitoring plans and Novartis procedures • Conduct site initiation visits and provide ongoing training for site personnel • Perform continuous on-site and remote monitoring for protocol, GCP, regulatory, and 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 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

🎯 Requirements

• Minimum of 3 years’ experience in site monitoring • BS/BA degree in 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 communicator and presentation skills (oral and written) • Fluent in both written and spoken English • Must have a fully valid and unrestricted driver’s license • Willingness and ability to travel by plane or car up to 80% of the time • RLT, CAR T or Oncology experience a plus

🏖️ Benefits

• Performance-based cash incentive • Eligibility to be considered for annual equity awards, depending on role level • 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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