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Tier-1 brand, mid-level generalist role, metro location and broad skillset increase applicant competition.
Strong clinical trial domain and CDISC/EDC knowledge make skills less transferable across industries.
Explicit 5+ years clinical trial reporting requirement plus mandatory SAS, CDISC and domain skills increases filter strictness.
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Manage multiple clinical trial studies across various Therapeutic Areas, serving as primary liaison for stakeholders.
Own end-to-end report development and delivery including requirements gathering, development using SAS, elluminate Mapp, Qlik, and quality assurance ensuring timely and compliant outputs.
Drive efficient reporting solutions by collaborating with clinical teams, prioritizing deliverables, and maintaining adherence to SDLC and organizational processes.
Bachelor's degree in Computer Science, Mathematics, Statistics, Life Sciences, Programming, Data Management or related analytical discipline.
5+ years of experience in reporting and analytics development focused on clinical trials within the pharmaceutical industry.
Proficiency in SAS, Qlik, SQL/PLSQL and familiarity with elluminate Mapper; strong understanding of relational databases and ETL concepts.
Experience working with clinical data sources and understanding of clinical trial protocols; knowledge of CDISC standards (SDTM) and experience with EDC systems such as RAVE or Oracle Clinical.
Experienced in handling multiple clinical trials reporting projects independently and acting as a key stakeholder interface for requirements and deliverables.
Technical expertise in advanced analytics tools and programming languages, with proven ability to lead complex report development and testing in compliance with SDLC.
Strong domain knowledge in clinical trial data environments, regulatory standards (ICH, FDA), and therapeutic areas to align reporting with clinical objectives.