Clinical Trials Data Specialist

Job Summary

Working remotely on a full-time basis, the Junior Clinical Trials Data Specialist will review patient clinical records to determine trial matches, manage workflows, and collaborate with cross-functional teams to create clinical reports.

Key responsibilities

• Review patient clinical records and determine clinical trial matches
• Manage clinical trial workflows independently, adapting to changing priorities
• Collaborate with scientists, pathologists, and product development teams to create customized clinical reports

Required qualifications

• Bachelor's or Master's degree in Genetics, Molecular Genetics, Cancer Biology, or Biological Sciences
• Willingness to work flexible hours and adapt to business needs
• Ability to manage complex tasks efficiently under time constraints
• Self-motivated and able to thrive independently as well as within a collaborative team
• Demonstrated passion for making an impact in a fast-paced, mission-driven environment