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Job Description
Precision for Medicine is seeking a Clinical Scientist to perform early and continuing scientific review of clinical data. This role supports overall data quality and consistency by applying the protocol and oncology standards. The Clinical Scientist will work remotely from Poland, Hungary, Serbia, Romania, or Slovakia.

Responsibilities:
  • Reviews subject data for accuracy per protocol and oncology standards.
  • Maintains relationships with project team members.
  • Collaborates with Medical Monitors and other departments on data capture trends.
  • Provides input into project documentation.
  • Supports the development and UAT of data outputs.
  • Assists with scientific, clinical, oncology-related questions.
  • Provides status updates and escalates issues.
  • Identifies quality risks and recommends corrective actions.
  • Conducts UAT of programming output.
  • Reviews clinical trial data sources for consistency and accuracy.
  • Issues and resolves queries in EDC systems.
  • Communicates data quality issues and implements actions.
  • Provides study-specific training for project teams.
  • Develops monitoring and data review tools.
  • Participates in team meetings.
  • Reviews dictionary coding.
  • Establishes task tracking metrics.
  • Ensures eTMF documentation is managed.

Requirements:
  • Bachelor’s degree in science or healthcare.
  • Proficiency in medical terminology.
  • Two years in clinical operations, data management, or related discipline.
  • Experience in oncology clinical research.
  • Experience as a Clinical Research Associate (CRA) or Study Coordinator/Research Nurse preferred.
  • Oncology therapeutic experience.
  • Experience in phase I, II and III oncological trials preferred.
  • Experience with electronic data capture systems (EDC) and data visualization tools preferred
  • Computer proficiency
  • Working knowledge of FDA & ICH/GCP regulations and guidelines.

The role offers:
  • Remote work opportunity
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