About the Role:We are looking for a highly experiencedClinical Data Management or Biostatistics Programming Consultantto serve as adomain expertin oncology clinical trials. In addition to guiding traditional data review practices, you will play a critical role in shaping anAI-based tool for clinical data review , helping define logic, workflows, and quality standards informed by real-world practices.Location: Pune, India (Remote flexibility available) Engagement Type: Part-time / Project-based Contract (3–6 months, extendable)About the Company:Dizzaroo Pvt Ltdis a fast-growing AI-first startup dedicated to transforming the pharmaceutical and life sciences industry. With deep roots in clinical research and drug development, we focus on building intelligent tools to optimize processes across the drug development lifecycle—from discovery to commercialization. Our mission is to combine domain expertise with cutting-edge AI to solve real-world problems at scale. Key Responsibilities:Act as thesubject matter expertin oncology clinical data review to guide development of an AI-powered review platform. Design and document aClinical Data Review Plan (DRP)aligned with oncology trial standards. Interpret and reviewCDISC SDTM datasets , ensuring accurate and relevant data mapping. Collaborate with AI/ML engineers totranslate clinical knowledge into review logic, quality rules, and validation checks . Write and testSQL and/or R scriptsto support interim data reviews and tool validation. Provide strategic input intorisk-based monitoring and centralized review methodologies . Required Qualifications:Master’s degree inBiostatistics, Data Science, Public Health, Life Sciences , or related fields. Minimum3 yearsof relevant experience inclinical data management or statistical programming , with at least2 years in oncology trials . Strong familiarity withCDISC SDTM datasets . Hands-on programming experience inSQL and/or R . Understanding of industry-standarddata review processes and workflowsin sponsor or CRO settings. Preferred Qualifications:Experience in building or contributing toData Review Plans (DRP)orData Management Plans (DMP) . Familiarity withPinnacle 21, SAS , or other data validation tools. Prior collaboration with AI or software teams in health/life sciences projects. Strong documentation and communication skills. What You Get:A chance towork at the intersection of clinical science and cutting-edge AI , contributing to a transformative product. Flexible remote work arrangement withcollaborative, intellectually curious peers . Direct influenceon tool design, logic, and performance. Competitive consulting fee andpotential for longer-term collaboration . Opportunity tobuild portfolio and visibilityin the AI-healthcare ecosystem. Engagement Details:Duration:3–6 months(extendable) Estimated Commitment:10–20 hours/week Location:Pune-based preferred; remote candidates welcome Compensation:Competitive and commensurate with experience How to Apply:Please send yourCVand a shortcover lettersummarizing your relevant experience to dhirajg@.
Job Title
Consultant – Clinical Data Review AI Tool Development (Oncology Trials)