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.