Clinical Trial Data Analyst

Description:

We are seeking a 𝗖𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝗧𝗿𝗶𝗮𝗹 𝗗𝗮𝘁𝗮 𝗔𝗻𝗮𝗹𝘆𝘀𝘁 to support our mission of advancing healthcare research and patient centered care. In this role, you will manage and analyze clinical trial data, ensuring integrity, compliance and usability. You will also contribute to developing AI ready datasets that fuel Victreats cutting edge treatment navigation solutions.

𝗪𝗶𝘀𝗵𝗹𝗶𝘀𝘁 𝗳𝗼𝗿 𝗖𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝗗𝗮𝘁𝗮 𝗔𝗻𝗮𝗹𝘆𝘀𝘁

*Design and implement data management plans & protocols to ensure high quality data collection and analysis throughout the clinical trial lifecycle.

*You possess deep operational knowledge of the end to end clinical trial data lifecycle, gained from direct experience within a CRO or pharmaceutical sponsor environment.

*Design and implement a data mapping framework that converts clinical trial datasets from multiple sources into a standardized format for our AI tools.

*Perform data validation and cleaning, identify discrepancies and resolve data related issues to maintain data integrity.

*Prepare and manage datasets for integration into AI tools and contribute to real world evidence (RWE) analysis in healthcare.

*Ensure compliance with clinical protocols and regulatory standards.

*Collaborate with clinical operations, biostatistics, and medical teams to align trial data with our custom AI models.

*Conduct statistical analyses and generate reports that communicate findings to stakeholders and enhance decision making processes.

*Utilize advanced data visualization tools to present complex data clearly and concisely to both technical and non technical stakeholders.

𝗪𝗵𝗮𝘁 𝘄𝗲 𝗮𝗿𝗲 𝗹𝗼𝗼𝗸𝗶𝗻𝗴 𝗳𝗼𝗿

*Bachelor’s or Master’s degree in Biostatistics, Biotechnology, Bioinformatics, Public Health or related field.

*Must have deep operational knowledge of the full clinical trial data lifecycle from direct CRO or pharma experience.

*Proficient in statistical analysis software (e.g., SAS, R or Python) and data visualization tools (e.g., Tableau, Power BI)

*Strong understanding of clinical trial processes and regulatory requirements and guidelines/compliance (e.g., ICH, GCP)

*Prior Experience in large scale clinical trial data analysis

*Ability to convert data from diverse clinical trial sources into standardized formats.