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Tier-1 pharma, mid-level 5+ clinical analytics role in Hyderabad creates high candidate competition.
Strong clinical trial and CDISC domain requirements make cross-industry transfers difficult.
Requires 5+ years in pharmaceutical clinical reporting plus SAS, CDISC, and SDLC experience, enforcing strict shortlisting.
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Manage multiple clinical study reporting projects across various Therapeutic Areas as the primary stakeholder contact.
Own end-to-end report development and delivery, from gathering requirements to developing SAS, Qlik, and Elluminate Mapp reports ensuring adherence to timelines and quality standards.
Drive efficient and compliant clinical reporting and analytics solutions while collaborating globally and prioritizing deliverables critical to business needs.
5+ years experience in pharmaceutical industry clinical trial reporting and analytics.
Degree in Computer Science, Mathematics, Statistics, Life Sciences, Programming, Data Management, Scientific or Analytic discipline.
Proficiency in SAS, Qlik, SQL/PLSQL; experience with Elluminate Mapper is an advantage.
Strong understanding of relational databases, ETL, clinical data sources (e.g. EDC, labs, IVRS/IRT), and knowledge of CDISC standards (SDTM) preferred.
Experienced in collaborating with clinical stakeholders and interpreting clinical trial protocols to define reporting requirements.
Demonstrates strong technical expertise in clinical data analytics tools and SDLC processes for high-quality report development.
Able to work flexibly with global teams across time zones and prioritize reporting efforts aligned with study and business priorities.