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Manager, Csar - Sas Clinical Data Reporting And Spotfire Programmer

6-8 years
Not Disclosed
10 May 1, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title: Manager, CSAR – SAS Clinical Data Reporting and Spotfire Programmer

Location: India – Hyderabad (On Site)
Job ID: R-212019
Date Posted: April 4, 2025
Category: Research


Job Summary

Amgen is seeking a Manager, CSAR with expertise in SAS programming and Spotfire data visualization to support clinical data reporting activities. This role ensures delivery of high-quality data reports and dashboards aligned with Amgen’s procedures and regulatory requirements. The manager will contribute both strategically and operationally, collaborating with cross-functional teams and supporting system transformation projects in global development operations.


Key Responsibilities

  • Develop and maintain SAS clinical data reports and Spotfire dashboards

  • Collaborate with data management and clinical study teams to meet deliverables

  • Lead and support decision-making through data science insights

  • Provide technical leadership for clinical trial systems and programming platforms

  • Create documentation (SOPs, policies), support audits, and contribute to quality initiatives

  • Support clinical trial platforms such as Rave EDC and Veeva EDC

  • Participate in cross-functional collaborations, delivering study-level and portfolio-level results

  • Drive continuous improvement and process innovation in reporting workflows


Required Knowledge and Skills

  • Strong hands-on skills in SAS programming and Spotfire visualizations

  • Understanding of clinical trial processes, GCP, regulatory filings, and clinical database systems

  • Familiarity with project management, audit compliance, and risk analysis

  • Experience with data-driven decision-making and cross-functional team collaboration


Basic Qualifications

  • Bachelor’s degree in Life Sciences, Computer Science, or a related field with 6–8 years of experience

  • OR Master’s degree with 4–6 years of experience

  • Clinical research experience in biotech/pharmaceutical/CRO setting

  • Expertise in life sciences or a medically related domain


Preferred Qualifications

  • Advanced degree in life sciences, statistics, or computer science

  • Experience managing CROs and third-party vendors

  • Strong organizational, analytical, and problem-solving skills

  • Project planning and oversight of large-scale transformation initiatives