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Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Clinical Trial Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • A bachelor's degree is required; a degree in health or medical science or nursing is preferred.
  • Previous experience providing the knowledge, skills, and abilities to perform the job, comparable to 0 to 1 year.
  • Ability to work in a team or independently as required.
  • Flexibility to reprioritize workload to meet changing project timelines.
  • Ability to attain and maintain a solid understanding of applicable country regulations, International Council for Harmonisation Good Clinical Practice guidelines, and organization/client standard operating procedures and work practice documents.
  • Good English language and grammar skills, and proficient local language skills as needed.
  • Good digital literacy and proficiency in Microsoft Office, including Word, Excel, and PowerPoint, with the ability to learn clinical trial database systems.
  • Effective oral and written communication skills.
  • Judgment and decision-making skills.
  • Ability to accurately follow project work instructions.
  • Australian citizenship or permanent residency is required.

Responsibilities

  • Perform department, internal, country, and investigator file reviews as assigned, and document findings in appropriate systems.
  • Ensure allocated tasks are performed on time, within budget, and to a high-quality standard; proactively communicate risks to project leads.
  • Provide system support, including Activate and the electronic Trial Master File, and ensure system databases are current.
  • Perform administrative tasks on assigned trials, including timely processing of documents sent to the client electronic Trial Master File, performing electronic Trial Master File reviews, distributing mass mailings and communications as needed, and providing documents and reports to internal team members.
  • Support scheduling of client and internal meetings as needed.
  • Review and track local regulatory documents as needed.
  • Maintain vendor trackers.
  • Support the start-up team in regulatory submissions.
  • Work directly with sites to obtain documents related to site selection.
  • Collaborate with teammates and appropriate clinical personnel to achieve project goals and address site issues and risks.

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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