This is a fully remote position, open to applicants in Argentina.

📋 Description

• Support the Data Management Study Lead in creating eCRF, Data Validation Specifications, and Study Specific Procedures.

• Evaluate clinical and third-party data according to edit specifications and data review strategies.

• Generate clear, accurate, and concise inquiries to investigational sites.

• Communicate efficiently with colleagues, clinical data scientists, and functional management.

• Execute project tasks such as organizing and archiving study documentation, as well as sending queries to investigator sites for resolution.

• Ensure adherence to study timelines.

⛳️ Requirements

• Bachelor's degree in a relevant discipline, such as Life Sciences or Healthcare.

• Fundamental understanding of clinical data management within the pharmaceutical or biotechnology sectors.

• Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar).

• Strong attention to detail and capability to thrive in a high-paced environment.

• Exceptional communication abilities and capacity to work collaboratively with cross-functional teams.

• Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is advantageous.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellbeing programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellbeing resources.

• Opportunities for learning and development through structured training and career pathways.