Clinical Research Associate II, Bilingual, Oncology

🕒 June 5

🐊 Florida – Remote

🐊 Florida – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 45%

What it means: how likely this posting is sitting open without active hiring.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

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation • Monitor investigator sites with a risk-based monitoring approach • Escalate observed deficiencies and issues to clinical management, following all issues through to resolution • Ensure that required essential documents are complete and in place, according to ICH-GCP and applicable regulations • Provide trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required

🎯 Requirements

• Must live in the South/ SE region of the US and have a minimum of 1 year travel monitoring experience in Oncology • Must be Bilingual (English/ Spanish) • Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 year as a clinical research monitor) or completion of PPD Drug Development Fellowship • Valid driver's license where applicable

🏖️ Benefits

• Frequent drives to site locations • Frequent travel, generally 60-80% but more for some individuals • Extended overnight stays required • Personal protective equipment required such as protective eyewear, garments and gloves