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Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Research Physician 2

Physicians & SurgeonsConfirmed live in the last 24 hours
Part-timePrague, CzechiaNo salary listedIn-person

About the Job

Requirements

  • A valid medical degree and registration within the country of practice are required.
  • A medical license in good standing with an unrestricted ability to practice at the place of work is required, where applicable.
  • A valid International Council for Harmonisation Good Clinical Practice certificate is required.
  • General medical practitioner diagnosis and treatment proficiency is required; no prior clinical research experience is required.
  • A good understanding of medical terminology, drug safety, and interpretation of laboratory reports is required.
  • Computer proficiency, including confidence using Microsoft Office and sponsor-related programs and portals, is required.
  • Good administration skills and attention to quality and detail are required.
  • The candidate must be able to work under pressure and meet deadlines.
  • The candidate must understand commercial and financial concepts and their business impact.
  • The candidate must work well with others, assist in other areas as needed, learn new processes and systems quickly, think, read, learn, reason and interpret effectively, work independently, and prioritize and multitask.

Responsibilities

  • Conduct clinical trials according to ICH GCP, local regulations, study protocols, and company processes.
  • Ensure the medical wellbeing and safety of participants through safe study performance and execution.
  • Maintain clinical oversight and quality for registered studies and deliver study targets, including recruitment, enrollment, and participant retention.
  • Carry out clinical evaluation and assessment of participants to determine eligibility for enrollment in studies.
  • Review enrollment progress, pre-screening and screening success rates, screen failure rates, participant safety, and retention.
  • Interpret protocols and Investigator’s Brochures and participate in initiatives to strategize for patient recruitment.
  • Protect participant welfare and safety through ethical conduct, giving this highest priority throughout all aspects of each study.
  • Fulfill and comply with medical duties according to protocols, SOP/COP, ICH GCP, and local regulations.
  • Report safety threats that may affect stakeholders or participants, and handle complaints or quality incidents according to site processes.
  • Record information meticulously and manage source documentation.
  • Participate in audit preparations and site inspections.
  • Oversee management of investigational medical products.

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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