Senior Medical Writer

About Us

Axtria is a global cloud software and data analytics company focused on life sciences. Within Clinical Solutions, we are scaling Axtria Rapid CSR, a GenAI?powered capability that helps medical writers produce high?quality, ICH?aligned CSR sections 3050% faster by orchestrating multi?source clinical inputs (TLFs, protocols, SAPs) with human?in?the?loop validation

Role Overview:

We are seeking an experienced Medical Writer to lead the LLM powered authoring of Clinical Study Reports (CSRs) and clinical trial documents. This is a client-facing role requiring strong scientific writing expertise, regulatory knowledge, and familiarity with emerging GenAI technologies for medical writing automation.

Key Responsibilities:

• Client discovery, scoping, and requirements (business?side)
• Lead requirements elicitation with client Medical Writing/Regulatory teams for CSR authoring (template standards, TA nuances, target sections, review cadence, acceptance criteria, quality bars).
• Translate business goals (timelines, submission strategy, risk tolerance, review workflows) into clear deliverables and negotiate scope, timelines, and costs; manage change requests and approvals.
• Define done for each CSR section (e.g., Safety Evaluation, Efficacy) including scientific tone, numerical consistency, and ICH E3 alignment; maintain a living Requirements & Assumptions log
• Translation to technical work (internal hand?off)

• Convert business requirements into technical briefs for the GenAI Engineer (priority TLFs, required tables/figures, prompt constraints, style rules, traceability links to sources)
• Specify validation frameworks for GenAI outputs (accuracy, completeness, faithfulness, numerical parity with TLFs) and co own evaluation rubrics with engineering.
• Own the backlog for Rapid CSR features during engagements (as Business PO), prioritize bugs/iterations based on medical writing impact and regulatory readiness
• Run structured review cycles (internal QC client SME review stat review) and close comments to final

Location: Pune, Gurugram, Noida, Hyderabad, Bengaluru

Required Skills and Qualification:

• Advanced degree in Life Sciences, Pharmacy, or related field.
• Proven track record (812 years) in CSR authoring and regulatory writing.
• Strong understanding of clinical trial processes and regulatory guidelines.
• Working knowledge of GenAI/LLMs and AI/ML SDLC (prompts, evaluation, HIL review, versioning).
• Comfort with clinical data sources (TLFs, SAP, protocol, narratives) and numerical consistency checks
• Excellent planning, negotiation, and stakeholder management skills.

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Soft Skills:

• Work closely with cross-functional teams, including clinical data engineers, clinical data modelers, front end developers, QA/CSV specialists, clinical SMEs, project managers, and cloud/infrastructure professionals, to understand project requirements and deliver high-quality solutions.
• Maintain thorough documentation of methodologies, processes, and results of the models. Prepare and present detailed reports on assigned projects to stakeholders, including client and internal leadership illustrating the impact and effectiveness of data-driven strategies.

Why Join Us

• Be the bridge between clients and engineering, shape what next?gen CSR authoring looks like.
• Write at scale with GenAI tools, while setting the gold standard for accuracy, traceability, and compliance.
• Work cross?functionally with Clinical Ops, Biostats, and AI Engineering to bring Rapid CSR into production at top biopharma clients