
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
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.
🕒 May 14
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10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
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.
• Monitors investigator sites with a risk-based monitoring approach • Conducts monitoring tasks in accordance with the approved monitoring plan • Participates in the investigator payment process • Ensures audit readiness and develops collaborative relationships with investigational sites • Keeps in contact with investigative sites to confirm that the protocol is being followed
• Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent • 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.
• Health insurance • Paid time off • Remote work options
Apply Now🕒 May 13
CRA II at ICON conducting clinical trial monitoring and ensuring compliance while collaborating with site staff. Analyzing clinical data and contributing to innovative treatments and therapies.
🕒 May 12
Lead CRA overseeing complex clinical studies ensuring compliance with clinical protocols and regulations. Collaborate cross-functionally to manage site selection, monitoring, and training within life sciences.
🇺🇸 United States – Remote
💰 $24M Grant on 2020-07
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🦅 H1B Visa Sponsor
🕒 May 12
Clinical Research Associate supporting clinical trials and regulatory submissions for Kuros Biosciences. Overseeing study tracking tools and ensuring compliance with clinical regulations.
🕒 May 8
CRA at ICON conducting clinical trial monitoring and collaborating with investigators. Responsible for ensuring protocol compliance and high-quality clinical data.
🕒 May 8
Clinical & Endpoint Research Associate coordinating site evaluations and travel. Working closely with Clinical Trial Managers and ensuring data quality for clinical studies.
🇺🇸 United States – Remote
💵 $60k - $70k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🦅 H1B Visa Sponsor