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

Beschreibung

• 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.