Senior Clinical Data Engineer for Trials

Otsuka Pharmaceutical Co., Ltd; Palo Alto (CA); On-site; USD 146,000 - 156,000; Full time

Job summary

ReCor Medical seeks a Senior Clinical Programmer to design, develop, and maintain clinical data management systems supporting regulatory submissions and data integrity across trials.

The role requires 5+ years in clinical data programming, proficiency in R, Python, SQL, SAS, and CDISC SDTM/ADaM. You will collaborate with cross-functional teams and help ensure FDA readiness through robust data processing and reporting.

Qualifications

• Bachelor’s degree in computer science, statistics, life sciences or related field; or Master’s with relevant experience.
• Proficiency in R, Python, SQL, SAS; strong understanding of clinical data standards (CDISC SDTM, ADaM).
• Experience preparing programming deliverables for regulatory submissions; strong communication skills.

Responsibilities

• Design and develop apps, scripts, and tools for clinical data collection, processing, and analysis.
• Maintain data standardization practices (CDISC SDTM/ADaM) across trials.
• Collaborate with clinical operations, biostatistics, and regulatory affairs teams.
• Generate reports and visualizations for clinical studies and regulatory submissions.
• Create and maintain data integration pipelines between clinical systems and databases.
• Provide guidance to junior programmers on data processing methodologies.

Skills

R

Python

SQL

SAS

CDISC SDTM ADaM

Regulatory understanding

Communication skills

Education

Bachelor's degree in computer science, statistics, life sciences

Master's degree with 3 years experience

Tools

Power BI

Tableau

Git

Cloud platforms

Job description

ReCor Medical seeks a Senior Clinical Programmer to design, develop, and maintain clinical data management systems supporting regulatory submissions and data integrity across trials.

The role requires 5+ years in clinical data programming, proficiency in R, Python, SQL, SAS, and CDISC SDTM/ADaM. You will collaborate with cross-functional teams and help ensure FDA readiness through robust data processing and reporting.