CRA II/Sr CRA I/Sr CRA II – Multiple Therapeutic Areas

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🐊 Florida – Remote

🐊 Florida – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 15%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

🏥 Healthcare

Biotechnology • Pharmaceuticals • Healthcare

Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.

📋 Description

• Perform and coordinate all aspects of the clinical monitoring and site management process • Conduct remote or on-site visits to assess protocol and regulatory compliance • Manage required clinical trial documentation • Manage procedures and guidelines from different sponsors and monitoring environments • Serve as a site processes specialist • Ensure trials follow approved protocols, ICH-GCP guidelines, applicable regulations, and SOPs • Protect subjects' rights and well-being and ensure data reliability • Ensure audit readiness • Develop collaborative relationships with investigational sites • Perform frequent drives to site locations and travel, generally 60–80%, potentially including extended overnight stays • Work in office, laboratory, clinical, and/or home office environments • Handle potential exposure to biological fluids and infectious organisms using required personal protective equipment

🎯 Requirements

• Bachelor's degree in a life science related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification • Approximately 1 year of experience as a clinical research monitor or completion of PPD Drug Development Fellowship • 1–2 years of traveling on-site monitoring experience • Valid driver's license where applicable • Therapeutic experience in at least one of: Oncology, Ophthalmology, Neurology, Cardiology, Rare Disease, Respiratory, Obesity, and/or Pulmonary • Live within 60 miles of the nearest major airport • Able to travel up to 80% • Legally authorized to work in the United States without sponsorship • Able to pass a comprehensive background check, including drug screening • Proven clinical monitoring skills • Understanding of medical/therapeutic area knowledge and medical terminology • Working knowledge of ICH GCPs, applicable regulations, and procedural documents • Critical thinking, root cause analysis, and problem-solving skills • Ability to manage Risk Based Monitoring concepts and processes • Good oral and written communication skills • Customer focus, listening skills, attention to detail, and ability to identify underlying issues • Organizational and time management skills • Effective interpersonal skills • Flexibility and adaptability • Ability to work independently or as part of a team • Solid knowledge of Microsoft Office and ability to learn appropriate software • Good English language and grammar skills • Good presentation skills

🏖️ Benefits

• Fully remote work mode • Standard Monday–Friday work schedule • Opportunity to work with global teams and support clinical trials across multiple therapeutic areas • Professional experience through clinical monitoring and site management • Exposure to diverse sponsors and monitoring environments (FSO, FSP, Government) • Up to 80% travel-related work opportunities

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