Company: Thermo Fisher Scientific
Division: PPD Clinical Research Services
Location: Bangalore, Karnataka, India (Fully Remote)
Job Type: Full-Time
Category: Clinical Research | Clinical Data Management | Biostatistics
Experience Required: Minimum 4+ years in clinical data programming, statistical programming, or clinical data management
Role Overview
A globally recognized Contract Research Organization (CRO) is seeking a highly skilled CDM Programmer II with strong expertise in Python, R, and SAS programming. This fully remote opportunity is ideal for professionals experienced in clinical data management, database programming, and statistical analysis within pharmaceutical or biotechnology environments.
The selected candidate will contribute to database development, edit check programming, data validation, and automation initiatives supporting global clinical trials. This role requires technical proficiency, regulatory awareness, and the ability to collaborate within multi-disciplinary project teams.
Key Responsibilities
Design, build, and test clinical study databases and edit checks.
Develop and optimize programs using Python, R, and SAS for clinical data analysis and reporting.
Perform data extraction, transformation, cleaning, and validation from multiple clinical data sources.
Create and test listings for data review and quality checks.
Conduct statistical analysis, including regression, hypothesis testing, and multivariate analysis.
Develop reusable scripts, macros, and automation tools to improve operational efficiency.
Ensure compliance with Good Clinical Practice (GCP) guidelines and internal SOPs.
Support moderately complex clinical studies under supervision and contribute to simple study leadership activities.
Collaborate with cross-functional teams including data managers, statisticians, and clinical operations.
Document programming processes, validation steps, and analytical outputs.
Participate in process improvement initiatives to enhance data quality and system efficiency.
Education & Experience
Bachelor’s degree in Life Sciences, Biostatistics, Computer Science, Data Science, or related discipline.
Minimum 4+ years of relevant experience in clinical data programming or statistical programming within pharmaceutical, biotech, or CRO settings.
Equivalent combinations of education, training, and directly related experience may be considered.
Technical Skills & Competencies
Strong hands-on expertise in Python, R, and SAS programming.
Solid understanding of relational database systems (RDBMS) and database structures.
Experience with clinical data management systems and EDC platforms.
Strong statistical knowledge including regression modeling and hypothesis testing.
Familiarity with regulatory standards including ICH-GCP.
Excellent analytical, troubleshooting, and problem-solving skills.
Strong organizational skills with the ability to manage multiple projects and deadlines.
High attention to detail and commitment to data integrity and quality.
Effective communication and cross-functional collaboration abilities.
Work Environment
Fully Remote (India-based role)
Standard Monday to Friday schedule
Occasional travel may be required depending on project needs
Virtual office environment with exposure to standard IT and database systems
Why Join This Organization?
Thermo Fisher Scientific is a global leader in life sciences, serving pharmaceutical and biotechnology clients worldwide. Through its clinical research division PPD, the organization supports over 2,700 clinical trials across 100+ countries, partnering with top pharmaceutical companies and emerging biotechs.
Employees gain exposure to global clinical development programs, innovative data technologies, and opportunities for professional growth within a science-driven environment focused on improving patient outcomes.
Equal Opportunity & Accessibility
The organization provides reasonable accommodations to individuals with disabilities during the recruitment and employment process.
As an Equal Opportunity Employer, all qualified applicants will receive consideration without discrimination based on any legally protected status.
Apply via ThePharmaDaily.com
If you are an experienced clinical data programmer with strong Python, R, and SAS expertise seeking a remote CRO opportunity, apply now through ThePharmaDaily.com and advance your career in global clinical data management and biostatistics.
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