Clinical Data Scientist / Trial Lead

Role : Clinical Data Scientist / Trial Lead

Key Responsibilities

Lead clinical data management activities across assigned clinical trials, ensuring high-quality data acquisition, database design, and data integrity.

Act as a technical resource for Data Management (DM) and Risk-Based Monitoring (RBM) standards, tools, and reporting.

Collaborate with cross-functional teams, external vendors, and internal stakeholders to ensure timely, compliant, and efficient data management processes.

Ensure study-specific documentation is complete and maintained in the Trial Master File (TMF).

Support data cleaning, integrity monitoring, e-data processing, and database release according to SOPs and industry best practices.

Qualifications

Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Clinical Research, or related field.

3+ years of experience in Clinical Data Management within the pharmaceutical or CRO industry.

Strong knowledge of EDC systems, clinical trial processes, and regulatory compliance (ICH-GCP).

Experience in Risk-Based Monitoring (RBM), data cleaning, and data visualization tools.

Excellent analytical, communication, and problem-solving skills.