Jobs at Perceptive

Provide nursing care and coordination for clinical imaging and experimental medicine studies: participant assessments, drug administration, cannulation, sample processing, study documentation, QC, and regulatory compliance (ICH-GCP). Support study setup, monitoring visits, and maintain training, emergency competency, and participant safety.

Provides GxP quality assurance oversight for a radiopharmaceutical production and clinical trial imaging facility. Responsibilities include QMS administration, deviation and CAPA review, document control, vendor qualification and audits, internal audits, batch record review and product release, training, quality metrics, risk management, regulatory inspection support, and continuous improvement. Requires GMP pharmaceutical experience, quality systems knowledge, strong communication, and the ability to work independently.

Operate, maintain and troubleshoot two Siemens RDS Eclipse cyclotrons and supporting systems (RNDS, ACS). Provide on-call and night-shift engineering support, manage spare parts inventory, ensure radiation protection and regulatory compliance, maintain documentation and SOPs, and support continuous technical improvement and training.

Supports demand generation and pipeline growth through marketing operations, campaign execution, CRM management, audience development, lead scoring, dashboard creation, event lead management, and performance analytics. The role partners with Growth, Sales, SDR, and Business Development teams to improve targeting, campaign effectiveness, lead quality, funnel conversion, and visibility into commercial performance.

Own UK business development for pre-clinical services, driving new business, strategic account growth, pipeline development, forecasting, proposals, and partnerships across biotechnology, pharmaceutical, and life sciences organizations. The role requires collaboration with scientific and operational teams, consultative selling, complex sales-cycle management, and commercial strategy development.

Lead design, implementation, and production operation of agentic LLM systems for medical imaging clinical trials. Build end-to-end agentic workflows (planning, retrieval, tool use), RAG solutions, evaluation frameworks, scalable backend services, and MLOps pipelines. Provide technical leadership, mentor engineers, ensure observability, compliance, and safety, and translate clinical workflows into validated, production-grade AI systems.

Design, build, and operationalize agentic AI systems for clinical imaging trials: intake/validation (DICOM/non‑DICOM), RAG-grounded workflows, QC checks, evaluation harnesses, MLOps deployment, observability, safety/traceability, and cross-functional enablement across the PDLC.