Jr. Clinical Trials Data Specialist - Remote

Overview

The Jr. Clinical Trials Data Specialist plays a crucial role in advancing precision medicine by reviewing clinical records and managing workflows to match patients with clinical trials.

In Short

• Review patient clinical records for clinical trial matches.
• Manage clinical trial workflows independently.
• Collaborate with cross-functional teams to create clinical reports.
• Synthesize information from multiple data sources.
• Ensure accuracy and clarity of clinical reports.
• Support ongoing and future team projects.
• Maintain flexibility and responsiveness to shifting workflows.
• Adapt to changing business needs.
• Contribute to a dynamic work environment.
• Perform other duties as assigned.

Requirements

• Bachelor's or Master's degree in relevant fields.
• Willingness to work flexible hours.
• Strong written and verbal communication skills.
• Proficient in critical thinking and problem-solving.
• Ability to manage complex tasks under time constraints.
• Highly detail-oriented and committed to accuracy.
• Self-motivated and able to work independently.
• Passion for making an impact in a mission-driven environment.
• Preferred experience in hematology/oncology clinical records.
• Basic knowledge of generative AI.

Benefits

• Full range of benefits including medical and incentive compensation.
• Restricted stock units offered depending on the position.
• Equal opportunity employer with non-discrimination policies.