Clinical Trials Data Specialist

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