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Thermo Fisher Scientific
Thermo Fisher Scientific
H1B Visa SponsorHealthcareLogisticsManufacturing
Thermo Fisher Scientific develops and delivers technologies, laboratory products, and pharmaceutical services that support scientific research and healthcare. Its work spans life sciences research, analytical problem-solving, laboratory productivity, diagnostics, and the development and manufacturing of therapies. The company serves customers through a global team and a portfolio of brands including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. Its careers encompass the scientific, healthcare, manufacturing, logistics, and service operations behind these offerings.
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FSP Clinical Research Associate I/II - Oncology (Remote, Israel)

Monitor oncology clinical trials for Thermo Fisher Scientific through remote and on-site site visits. Support regulatory compliance, data quality, documentation, and audit readiness across study sites.

ILIsraelRemoteFull-timeJuniorMiddleEnglish RequiredClinical Research

Description

  • Coordinate clinical monitoring and site management activities.
  • Conduct remote and on-site visits to evaluate protocol and regulatory compliance.
  • Apply risk-based monitoring methods at investigator sites.
  • Use root cause analysis and problem-solving to identify site process failures and develop corrective and preventive actions.
  • Verify data quality through source document review, source data verification, and case report form review.
  • Review investigational product inventories and related records.
  • Record observations in reports and letters, escalating deficiencies through resolution.
  • Maintain communication with investigative sites between monitoring visits.
  • Support investigator payment activities and investigator meetings.
  • Help identify qualified investigators and initiate clinical trial sites.
  • Complete trial closeout activities and retrieve study materials.
  • Confirm essential documents are complete and perform on-site file reviews.
  • Track study progress and provide trial status reports.
  • Maintain accurate study records in clinical trial management systems and other study platforms.
  • Coordinate communication between investigative sites, the client, and internal project teams.
  • Address company, client, and regulatory requirements, audits, and inspections.
  • Submit accurate expense reports and timesheets.
  • Support project publications, tools, process improvements, and other study-related initiatives.

Requirements

  • Bachelor’s degree in a life sciences discipline, Registered Nursing certification, or an equivalent relevant academic or vocational qualification.
  • At least minimal clinical monitoring experience comparable to two years in a clinical environment involving clinical trials, medical terminology, medical or clinical research, health care, or health sciences, with formal training in medical terminology and anatomy.
  • Valid driver’s license where applicable.
  • Experience in oncology.
  • Basic knowledge of medical or therapeutic areas and medical terminology.
  • Working knowledge of ICH Good Clinical Practice, applicable regulations, and procedural documents.
  • Clear oral and written communication skills, including communication with medical personnel.
  • Strong interpersonal, organizational, and time management skills.
  • Critical thinking, root cause analysis, and problem-solving abilities.
  • Ability to manage risk-based monitoring concepts and processes.
  • Ability to work independently and collaboratively.
  • Proficiency with Microsoft Office and ability to learn relevant software.
  • Strong English language and grammar skills.
  • Willingness and ability to travel frequently, generally 60–80%, with occasional overnight stays.
  • Ability to work in office, laboratory, clinical, and/or home-office settings.
  • Ability to use required personal protective equipment.

Benefits

  • Frequent travel of approximately 60–80%, potentially including extended overnight stays.
  • Remote work arrangement.
  • Standard Monday–Friday schedule.

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