Statistical Clinical Programmer

Boehringer Ingelheim
Ridgefield, CT, United States
5 days ago

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Experienced
Experience required
3 years minimum
Working hours
Regular working hours
Languages
English

Tech stack

Data Analysis Clinical Data Repository Data Transformation GXP

Job description

Experteer Overview You support end-to-end data work for clinical trials and related real-world data, transforming and analyzing data to enable decision-making. You collaborate with DP&V colleagues to deliver validated storytelling around data science aspects. The role emphasizes adherence to GxP, SOPs, and cross-functional teamwork within a global organization. This position offers the opportunity to contribute to transformative data-driven clinical development and to grow within a people-driven company culture. Compensation / Benefits * Transform, analyze, and report phase I-IV trial data, registries, and real-world data for specific use cases or assets * Stay current on new data transformation and analysis solutions and innovative tools within Boehringer Ingelheim * Present validated data science storytelling to DP&V colleagues * Ensure data transformation and analysis specifications meet completeness, correctness, SOPs, and GxP requirements * Support colleagues on data science tasks * Participate in cross-functional DP&V internal working groups and lead data science aspects * Promote cross-functional and team-based collaboration within DP&V Tasks * Bachelor’s degree with 3 years of data science experience OR MSC with related discipline * Senior role: Bachelor’s with 5 years in data science OR MSC with 3 years in pharma, CRO, regulatory, or academia * Experience in R or other software languages relevant to business needs * Understanding of clinical trial development process * Knowledge of statistical methodology, trial design, CDISC, and clinical data processing * Understanding and applying data science principles * Proven ability to plan, transform, analyze, interpret, and report clinical data * Fluent English (read/write/speak) and strong cross-cultural communication * Strong teamwork and interpersonal skills, with proactive problem-solving abilities Key requirements * role-specific discretionary bonus * relocation * comprehensive benefits * competitive compensation

Requirements

a * Participate in cross-functional DP&V internal working groups and lead data science aspects * Promote cross-functional and team-based collaboration within DP&V Tasks * Bachelor’s degree with 3 years of data science experience OR MSC with related discipline * Senior role: Bachelor’s with 5 years in data science OR MSC with 3 years in pharma, CRO, regulatory, or academia * Experience in R or other software languages relevant to business needs * Understanding of clinical trial development process * Knowledge of statistical methodology, trial design, CDISC, and clinical data processing * Understanding and applying data science principles * Proven ability to plan, transform, analyze, interpret, and report clinical data * Fluent English (read/write/speak) and strong cross-cultural communication * Strong teamwork and interpersonal skills, with proactive problem-solving abilities Key requirements * role-specific discretionary bonus * relocation * comprehensive benefits * competitive a Participate

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