AI agents for Healthcare, Pharma & Life Sciences.
52 jobs an AI agent can take off your team's plate — built, run, and supported by AI Labor Company.
Payer Operations & Claims (Commercial Health Plans, Blues, Regional Plans)
Gene & Cell Therapy CDMOs
- Patient scheduling coordination and chain of custody documentation for autologous CAR-T manufacturing
- EMA/FDA inspection readiness program for BLA/MAA-supporting manufacturing site
- Batch record review and disposition decision workflow for viral vector drug substance lots
- Tech transfer protocol documentation and process qualification batch campaign planning
- Clinical supply chain cold chain deviation investigation and patient impact assessment
- BLA/MAA module 3.2.A.2 facilities and equipment section authoring and maintenance
- Client-facing release testing COA compilation and sponsor QP certification package
FDA Regulatory Affairs (NDA/BLA/ANDA Submissions)
- FDA AdCom meeting preparation and briefing document quality review
- FDA Complete Response Letter gap analysis and resubmission planning
- ANDA paragraph IV certification strategy and patent litigation risk assessment
- REMS program design and FDA REMS submission package development
- eCTD compilation and publishing validation for NDA Module 5 clinical study reports
- Type A meeting request preparation and response management for clinical hold resolution
CROs Running Phase II/III Oncology Trials
- SAE narrative drafting and expedited safety reporting to FDA and EMA within 7/15 days
- Protocol deviation classification and CIOMS reporting to sponsor within 24 hours
- Risk-based monitoring signal detection and on-site visit prioritization
- eTMF completeness inspection readiness across 50+ active trial sites
Medical Devices Entering EU MDR / US FDA 510(k)
Pharmacy Benefit Managers (PBMs) & Specialty Pharmacy
- Prior authorization clinical criteria review and determination for specialty biologics
- Manufacturer rebate contract management and quarterly rebate invoicing reconciliation
- Drug utilization review (DUR) alert configuration and override documentation for retail network
- Biosimilar step therapy conversion outreach and clinical exception management
Integrated Delivery Networks (IDNs) & Health Systems
- Nurse float pool scheduling optimization and agency staffing minimization
- Charge capture reconciliation between OR documentation and Epic Resolute billing
- Prior authorization submission and follow-up for high-cost imaging and surgical procedures
- Payer contract load and fee schedule validation into Epic Tapestry
HEOR / Real-World Evidence (RWE) Shops
- RWE study protocol development and SAP finalization for Medicaid outcomes study
- Real-world safety signal detection and PSUR evidence contribution for European pharma client
- Comparative effectiveness analysis and indirect treatment comparison for HTA submission
- Budget impact model validation and payer scenario analysis for health technology submission
- CRO Phase-III clinical trial monitoring & EDC build
- Gene therapy viral vector manufacturing & quality release
- Manufacturing process validation & tech transfer (PV/TT)
- Companion diagnostic (CDx) co-development & IVD regulatory strategy
- Regulatory submission authoring & eCTD compilation
- Pharmacovigilance & ICSR case processing (E2B R3)
- Specialty pharmacy hub services & patient support program (PSP) ops
- Medical affairs publication planning & KOL engagement
- Clinical data management & CDISC SDTM/ADaM mapping
- HEOR modeling & payer dossier development
- Phase I SAD/MAD PK study conduct & PK/PD modeling
- Digital therapeutics (DTx) clinical evidence generation & FDA Breakthrough Device interactions
- Sterile manufacturing batch record review & release testing QC
- GxP-validated CSV & computer system validation (CSV/CSA)
- Biostatistical analysis & TLF package generation
- SaMD (Software as a Medical Device) 510(k) & IEC 62304 lifecycle documentation
- Medical device 510(k) premarket submission preparation