FSP Clinical Research Associate I/Clinical Research Associate II

🔥 11 minutes ago

🇮🇱 Israel – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 15%

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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 clinical monitoring and site management activities • Conduct remote and on-site investigator site visits to assess protocol and regulatory compliance • Manage sponsor procedures and guidelines across different monitoring environments • Ensure trials follow approved protocols, ICH-GCP guidelines, applicable regulations, and SOPs • Protect subjects’ rights and well-being and ensure data reliability and audit readiness • Monitor investigator sites using risk-based monitoring, including root cause analysis and corrective/preventive actions • Ensure data accuracy through source document review, source data verification, and CRF review • Assess investigational product inventory and records • Document observations in reports and letters and escalate deficiencies through resolution • Maintain contact with investigative sites between monitoring visits • Participate in investigator payment processes and investigator meetings • Help identify qualified investigators and initiate clinical trial sites • Perform trial closeout and retrieve trial materials • Ensure essential documents are complete and conduct on-site file reviews • Track trial status, provide progress updates, and maintain study systems such as CTMS • Facilitate communication among investigative sites, the client company, and internal project teams • Respond to company, client, and regulatory audits or inspections • Complete expense reports and timesheets • Assist with project publications, tools, process-improvement initiatives, and other project work

🎯 Requirements

• Bachelor's degree in a life sciences related field, or Registered Nursing certification, or equivalent relevant formal academic/vocational qualification • Equivalency may be considered through a combination of appropriate education, training and/or directly related experience • 1–2 years of experience as a Clinical Research Associate / Monitor • Valid driver's license where applicable • Basic medical/therapeutic area knowledge and understanding of medical terminology • Working knowledge of ICH GCPs, applicable regulations, and procedural documents • Good oral and written communication skills, including communication with medical personnel • Good interpersonal skills • Customer focus, listening skills, attention to detail, and ability to perceive underlying issues • Good organizational and time management skills • Flexibility and adaptability • Critical thinking, root cause analysis, and problem-solving skills • Ability to manage risk-based monitoring concepts and processes • Ability to work independently and in a team • Solid knowledge of Microsoft Office and ability to learn appropriate software • Good English language and grammar skills • Ability to travel frequently, generally 60–80%, including possible extended overnight stays • Ability to work in office, laboratory, clinical, and/or home office environments • Ability to use required personal protective equipment and work around biological fluids and potentially infectious organisms

🏖️ Benefits

• Fully remote work mode • Standard Monday-Friday work schedule • Remote and on-site work flexibility • Frequent travel expenses implied by required site travel • Personal protective equipment provided/required for applicable exposure conditions

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