Scientist Bioinformatics, Biology - Clinical Data Operations (m/f/d)- Foundation Medicine GmbH

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Ver: 255

Dia de atualização: 24-10-2024

Localização: Penzberg Bavaria

Categoria: Ciência Labor

Indústria: Biotechnology Medical Practice Hospital & Health Care

Posição: Mid-Senior level

Tipo de empregos: Full-time

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Conteúdo do emprego

Clinical Data Operations Associate (m/f/d)

PENZBERG, GERMANY

Foundation Medicinebegan with an idea—to simplify the complex nature of cancer genomics, bringing cutting-edge science and technology to everyday cancer care. Our approach generates insights that help doctors match patients to more treatment options and helps accelerate the development of new therapies. Foundation Medicine is the culmination of talented people coming together to realize an important vision, and the work we do every day impacts real lives. Foundation Medicine is headquartered in the heart of Cambridge, MA, USA. Since October 2017, Foundation Medicine GmbH in Penzberg has been actively supporting this mission.

Position Summary

The Clinical Data Operations Associate in Data Management performs operational and tactical support and ensures quality control and delivery of patient data to FMI’s Pharmaceutical and Academic research partners. The incumbent is responsible for accurate sample tracking and handling and timely data reporting and data entry that impacts the successful implementation and ongoing execution of FMI clinical partnerships. This role works closely with internal teams at FMI and external partner teams..
  • Provide ongoing study operational support.
  • Setup folder structure for all new studies in study repository/Trial Master File (TMF).
  • Monitor archiving of study documentation in study repository/TMF as study is ongoing and at closure.
  • Track sample processing and deliver study specific sample status reports (SST) to Clinical Program Leads identifying samples that have passed, are on hold, and/or have failed.
  • Monitor query process and query partners/collaborators to obtain missing information.
  • Complete Study Intake information in CRM/Clinical Trial Management System.
  • Manage sample return and destruction process for all Partners/Collaborators.
  • Bachelor’s Degree in a health or science field
  • 1+ year(s) of professional work experience in the science or health industry
  • Familiarity with oncology, clinical research, molecular biology, genetics and/or bioinformatics
  • Successful history of performing tasks under deadline pressure
  • Strong organizational, administrative, and analytical skills
  • Strong prioritization skills
  • Understanding of HIPAA and the importance of patient data privacy
  • You can expect a high degree of independence and a flexible working environment.
  • We stand for sincere and trust-based interaction with each other.
  • Your personal and professional development is very important to us.
  • All the advantages of a familiar work environment while being embedded in a large, global company.
We are looking forward to your application!
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Data limite: 08-12-2024

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