RAM Reporting Programmer II

Description

Summary: Seeking a detail-oriented RAM Reporting Programmer II to develop and deliver clinical data reporting solutions, ensuring high-quality data outputs for effective decision-making in a collaborative and data-driven environment. Highlights: 1. Contribute to cutting-edge science and innovation in clinical trials 2. Develop and deliver critical clinical data reporting and analytics solutions 3. Collaborate with diverse teams in a fast-paced, data-driven environment Job Description We are committed to saving and improving lives through cutting\-edge science and innovation. Within Global Clinical Data Integration (GCDI), the Reporting Mapping (RaM) team plays a critical role in enabling clinical trials through high\-quality data, reporting, and analytics solutions. Role Overview We are seeking aRAM Reporting Programmer IIto support the development and delivery of clinical data reporting solutions across global clinical trials. In this role, you will contribute todata validation, reporting standardization, and operational delivery, ensuring high\-quality clinical data outputs that enable effective data review and decision\-making. This position is ideal for atechnically strong and detail\-oriented professional who thrives in a collaborative, fast\-paced, and data\-driven environment. Key Responsibilities ✅ Reporting Development Delivery * Develop and maintain clinical reports and listings, including: * PDAM NG reports and validations * SDV and integrated reporting outputs * EDC and CDB listings * Deliver reporting solutions aligned with study timelines and requirements ✅ Data Quality Validation * Implement programmed data validation logic and discrepancy checks * Ensure data accuracy, consistency, and integrity across clinical systems * Support data review and issue resolution processes ✅ Clinical Trial Support * Contribute to reporting activities across the clinical trial lifecycle: * Study startup * In\-life execution * Closeout and database lock * Support initiatives such as CDDR, ECOA integrations, and Zero Gravity (ZG) reporting ✅ Standards Continuous Improvement * Maintain and enhance reporting libraries and standards (e.g., PDAM NG) * Contribute to process optimization and standardization efforts * Participate in validation and deployment of reusable reporting components ✅ Operational Execution * Manage service requests (SRs) and support reporting deployments * Troubleshoot technical issues and ensure production stability ✅ Collaboration * Partner with Clinical Data Scientists, Data Management teams, and global stakeholders * Review and clarify requirements (e.g., Data Validation Plans) to ensure accurate delivery Required Qualifications Education * Bachelor’s degree in Computer Science, Engineering, Life Sciences, or related field (or equivalent experience) Technical Skills * Experience with one or more: * SQL * SAS * CQL (Clinical Query Language) * Exposure to clinical reporting and data platforms, such as: * Veeva CDB * JReview * Cognos (InForm) * Power BI and data visualization tools * English speaking advanced skills. Functional Knowledge * Understanding of clinical data lifecycle processes * Familiarity with data validation methodologies and Data Validation Plans (DVPs) Preferred Qualifications * Experience in pharmaceutical or clinical research environments * Experience working with external data integrations * Knowledge of standardized reporting frameworks and libraries Skills Competencies * Strong analytical and problem\-solving capabilities * High attention to detail and quality focus **Required Skills:** Adaptability, Applied Engineering, Clinical Data Cleaning, Clinical Data Management, Clinical Quality Assurance, Clinical Reporting, Clinical Research, Clinical Trials, Collaborative Care, Customer\-Focused, Data Analysis, Database Development, Data Processing, Data Quality Assurance, Data Review, Data Validation, Data Visualization, Detail\-Oriented, Electronic Data Capture (EDC), Health Data Interoperability, Learning Agility, Mechatronics, Pharmacovigilance, PL/SQL (Programming Language), Process Optimization **Preferred Skills:** Current Employees applyHERE Current Contingent Workers applyHERE Search Firm Representatives Please Read Carefully Merck Co., Inc., Rahway, NJ, USA, also known as Merck Sharp Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre\-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. **Employee Status:** Regular **Relocation:** No relocation **VISA Sponsorship:** No **Travel Requirements:** No Travel Required **Flexible Work Arrangements:** Hybrid **Shift:** Not Indicated **Valid Driving License:** No **Hazardous Material(s):** no **Job Posting End Date:** 07/16/2026\*A job posting is effective until 11:59:59PM on the dayBEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFORE the job posting end date. **Requisition ID:** R401203