Senior Clinical Research Associate – Field Based

🕒 June 26

🐊 Florida – Remote

🐊 Florida – Remote

💵 $108.5k - $201.5k / year

⏰ Full Time

🟠 Senior

🔬 Research Analyst

🦅 H1B Visa Sponsor

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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

• Lead assigned sites as the primary point of contact throughout study delivery • Build strong relationships to ensure site performance, quality, and milestone achievement • Manage Phase I to Phase IV trials per monitoring plans and company procedures • Conduct site initiation visits and deliver ongoing training for site personnel • Perform remote and on-site monitoring to ensure compliance and patient safety • Maintain accurate documentation and update all clinical systems in a timely manner • Identify risks, resolve issues, and escalate concerns as needed • Collaborate with cross-functional teams to drive efficient study execution • Support timely data query resolution and ensure data accuracy • Act as a subject matter expert across study activities when required

🎯 Requirements

• Minimum of three years of clinical site monitoring experience • Minimum of Bachelor’s degree in science, healthcare, or a related field • Strong understanding of clinical research and drug development processes • Knowledge of ICH/GCP and 21 CFR regulatory requirements • Ability to manage multiple priorities and work independently • Strong site management, communication, and problem-solving skills • Fluency in English, written and spoken, Spanish highly desired • Ability to drive and travel extensively, up to 80%, in a company vehicle

🏖️ Benefits

• Health, life and disability benefits • 401(k) with company contribution and match • Generous time off package including vacation, personal days, holidays and other leaves