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Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Assistant Clinical Research Associate

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeBrisbane QLD, AustraliaNo salary listed

About the Job

Requirements

  • A bachelor's degree in a life science discipline or related field, or Registered Nursing certification or an equivalent relevant formal academic or vocational qualification.
  • Previous experience comparable to 0 to 2 years; an equivalent combination of appropriate education, training, and directly related experience may also qualify.
  • Basic medical or therapeutic-area knowledge and understanding of medical terminology.
  • Ability to attain and maintain working knowledge of ICH Good Clinical Practice, applicable regulations, and company procedural documents.
  • Effective oral and written communication skills and excellent English language and grammar skills.
  • Excellent interpersonal and customer-service skills.
  • Good organizational and time-management skills, attention to detail, and proven ability to handle multiple tasks efficiently and effectively.
  • Flexibility and adaptability, and ability to work in a team or independently as required.
  • Well-developed critical-thinking skills, including a critical mindset, in-depth investigation for root-cause analysis, and problem solving.
  • Proficient computer skills, good knowledge of Microsoft Office, and ability to learn and use appropriate software and modern technology.
  • Ability to extract pertinent information from study documents, electronic study-data systems, clinical trial management systems, and dashboards.
  • Australian citizenship or permanent residency is required.

Responsibilities

  • Complete assigned study and site-management activities in accordance with the task matrix, standard operating procedures, and study requirements.
  • Complete required study-specific training and become proficient in study systems.
  • Support site start-up activities, including pre-study assessments, site documentation, informed consent form customization, and vendor qualification.
  • Coordinate site readiness by managing system access, site-staff training, study supplies, and meeting logistics.
  • Review and maintain essential documents, site information, and study trackers to ensure data accuracy and regulatory compliance.
  • Support remote monitoring activities, including electronic medical record and electronic health record reviews, centralized monitoring, document reconciliation, and follow-up on missing study data.
  • Assist with site payments, invoice follow-up, and reconciliation of case report forms, queries, deviations, serious adverse events, and other study records.
  • Collaborate with clinical research associates, Clinical Leads, sites, and cross-functional teams to support study execution throughout the study lifecycle.
  • Complete administrative responsibilities, including timesheets, expense reports, and other assigned tasks.
  • Perform additional site-management or client-specific responsibilities as assigned.

About the Company

Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Thermo Fisher Scientific makes and sells the instruments, chemicals, consumables and lab services that drug companies, hospitals, universities and industrial labs use for research, testing and production. Its products cover work from gene sequencing and protein analysis to diagnostic tests and lab freezers, and its distribution arm ships supplies to labs worldwide. Drug developers also hire it to run clinical trials and to manufacture medicines under contract. It earns money from consumables that labs buy again and again, along with instrument sales, service contracts and outsourcing fees. The company traces its roots to Thermo Electron, founded in 1956, which merged with Fisher Scientific in 2006, and it is based in Waltham, Massachusetts.

Company size
10,001+
Company stage
IPO
Headquarters
Waltham, MA
Founded
1956

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