Raycaster

| About Raycaster Raycaster builds AI agents for life sciences. Backed by leading life sciences investors and YC, we’re already working with Agilent, Yokogawa Life Sciences and many leading instrument, CRO, CDMO, and biotech companies. Our platform helps teams move faster with audit-ready deliverables and compliant automation. The role (what you’ll do) We’re looking for a clinical trial operations expert (background in CRO, sponsor, or site) to design and validate workflows that support patient engagement, trial enrollment, and site coordination. You’ll help us translate real-world processes into repeatable workflows that our platform can automate and scale. Map end-to-end workflows in clinical trial enablement (pre-screening, recruitment, enrollment, site engagement, patient support). Define requirements for compliance (21 CFR Part 11, HIPAA, GDPR) and patient-facing communications. Work with Raycaster’s AI engineers to build and test “copilot” workflows. Provide subject-matter expertise on CTMS, EDC, IRT, and other systems integration. Help benchmark time savings, efficiency gains, and patient/PI satisfaction impact. You might be a fit if you have 3+ years in clinical operations, patient recruitment, or trial management (CRO, pharma, or site). Familiarity with CTMS/EDC systems and regulatory requirements for patient-facing tools. Experience leading initiatives that improved patient engagement, recruitment, or retention. Comfortable working at the intersection of clinical science, digital tools, and operational workflows. Why Join Us Shape how AI gets applied to real patient-facing workflows in clinical research. Collaborate with a fast-growing team building the first agentic platform for life science providers. Opportunity to see your workflows turned into production-ready copilots used by global CROs and sponsors.

| About Raycaster We build AI agents for life sciences. Backed by leading life sciences investors and YC, we’re already working with Agilent, Yokogawa Life Sciences and many leading companies to automate their regulated, complex processes to accelerate drug development. The role (what you’ll do) Partner with CMC teams to map current workflows end-to-end (inputs, systems, approvals, artifacts). Decompose tech-transfer packages (method revs, redlines/rationales, representative chromatograms, acceptance tests) into steps an AI can execute with citations. Capture validation/stability/release processes (accuracy/precision/linearity/LOQ, OOT rules, spec checks, CoAs) and translate them into checklists, schemas, and templates. Define data and document requirements (e.g., LIMS/CDS exports, S3/SharePoint/Vault locations), edge cases, and “fail-closed” rules (no source → no claim). Review AI-generated drafts for scientific correctness and compliance expectations (21 CFR Part 11). Create clear SOPs/playbooks for each automated workflow; iterate with engineers to reach “ready for pilot” quality. You might be a fit if you have 3 years in CMC/Analytical Development or QC, ideally touching Phase 2/3 or tech transfer to CRO/CMO/CDMO. Hands-on with HPLC/LC-MS (Ion-Pair, HILIC, AEX), method/SOP authoring, and interpreting system-suitability & chromatograms. Built or reviewed validation packets (ICH Q2(R1/R2)), stability trending/OOT, release specs/CoAs, and change control narratives. Operated in non-GMP → GMP handoffs; practical understanding of 21 CFR Part 11 expectations (audit trail, e-sig routing, data integrity). Familiarity with at least some of: Veeva Vault (or MasterControl), ELN/LIMS (Benchling, LabWare, SampleManager), CDS (Empower/Chromeleon), Jira/ServiceNow. Comfort collaborating with engineers; you enjoy turning tacit know-how into templates, schemas, and acceptance criteria. Nice to have ASO, mRNA/LNP, peptides, or oligo experience; Phase 3/registration exposure. Awareness of CSV (computerized system validation), ALCOA+, and doc control practices. Light data skills (reading CSVs, understanding units/columns) and curiosity about AWS/S3/Athena-style data lakes. Why this is interesting You’ll help design the cutting edge of audited AI workflows that save teams hours per artifact while keeping reviewers in control. Your fingerprints will be on how modern CMC gets done.