AI Clinical Scientist (Clinical Strategy & Evidence)

JobDescription / Summary Deep Intelligent Pharma (DIP) is an AI-native organization supporting globalpharmaceutical and biotech partners. We combine clinical judgement, scientificexpertise and AI-enabled workflows to accelerate evidence synthesis andclinical development decision-making. As an AI Clinical Scientist (Clinical Strategy &Evidence) , you will work closely with senior scientific experts on realclient programmes. This is not a clerical support role—you will contributeclinical reasoning and structured analysis to strategy discussions and keyR&D decisions. KeyResponsibilities · Interpret and synthesise clinical evidence (efficacy,safety, endpoints, unmet need, standard of care) and translate it intoactionable insights. · Support clinical development strategy (indication strategy,Target Product Profile thinking, protocol-level considerations, developmentpathway planning). · Conduct literature search, evidence mapping and structuredevidence synthesis using AI-assisted workflows. · Collaborate cross-functionally across discovery,preclinical, clinical and regulatory planning stakeholders. · Prepare scientific materials (briefs, slide decks,summaries) and support meetings with global clients and internal experts. · Maintain clear documentation and high-quality outputsaligned with project expectations and timelines. Requirements(Must Have) This role requires clinical judgement and interpretation of patient-care evidence; therefore, formal medical training and supervised clinical practice experienceare essential. · Accredited medical degree (MBBS/MD or equivalent) in Clinical Medicine from a recognized institution. · Completed structured hospital-based postgraduate clinicaltraining (e.g., residency/housemanship/standardised residency training/full clinicalrotations), with verifiable patient-care and clinical decision-makingexperience. · Strong analytical thinking and ability to communicateclinical rationale clearly and logically. · Proficient in English to review scientific literature, writeevidence summaries, and communicate with stakeholders. · Understanding of clinical research fundamentals; knowledgeof clinical trials and ICH-GCP is an advantage. Preferred/ Nice to Have · Clinical research experience (IIT or sponsor trials),exposure to medical monitoring, safety review, or protocol review. · Publications, guideline/consensus involvement, orevidence-based medicine (EBM) training. · Interest or experience in applying AI tools to literaturereview, evidence synthesis, or workflow automation.