Jobs at Discovery Life Sciences

Lead development and execution of LC-HRMS metabolite identification and biotransformation studies. Develop/optimize sample preparation and analytical workflows, operate and troubleshoot instrumentation, interpret complex MS/MS data, prepare scientific reports, and mentor laboratory staff while collaborating with Study Directors and sponsors.

Provide global leadership for pathology within Tissue Biomarker Services, harmonizing processes and standards, leading assay development/validation and clinical trial pathology, serving as Laboratory Director/PI, supporting clients and business development, and building a high-performing global pathology team across regions.

The VP of Pathology will lead a global pathology team, manage resources, optimize processes, and oversee the quality of pathology deliverables, including clinical trials and project evaluations.

The Pathologist will evaluate assays, interpret biomarker data, and support clinical trials, ensuring compliance in a regulated environment.

Serve as primary LabWare LIMS technical owner in a GxP-regulated lab: administer and configure LIMS, develop analysis templates and LabWare Basic scripts, integrate instruments, support validation (IQ/OQ/PQ) and change control, assist audits, manage user access, and maintain compliance with GAMP 5 and 21 CFR Part 11.

Manage and grow relationships with assigned clinical research sites, supervise CRCs, oversee site operations and monitoring, maintain regulatory documentation, partner with Quality and Regulatory teams, implement site performance and corrective action plans, and travel to sites to support study execution and site initiation/closure activities.

The Senior Financial Analyst will drive financial strategy, supporting decision-making and performance optimization, collaborating with teams to deliver insights and analyses.

Operate genomics laboratory workflows performing pre-analytical and analytical testing on various sample types. Maintain quality control, documentation, equipment maintenance, reagent preparation, and regulatory compliance (CLIA/CAP). Troubleshoot assays, support inventory and process improvements, and follow SOPs to ensure accurate data reporting and lab safety.

Manage setup and execution of clinical study projects: prepare proposals, cost/resource planning, coordinate contracts/MTAs/ethics approvals, set up projects per SOPs, supervise LIMS-based data management and invoicing, coordinate stakeholders, ensure on-time/on-budget delivery, and report to management.

Support coordination and management of clinical trials: maintain and archive study documentation, ensure regulatory and ethical compliance, communicate with the research team, prepare study reports, and translate/enter data into the clinical trial platform.

The Business Development Director will develop and close new business, manage client relationships, and coordinate strategic meetings in the preclinical sector.

Manage and validate clinical data in Salesforce and Excel, monitor and follow up on case queues, generate/reconcile reports, communicate with site coordinators and project managers, translate Bulgarian medical documentation, and ensure data privacy and regulatory compliance.

Manage receipt, registration, processing and shipment of clinical trial samples; track enrollment and consent; order tests in TALIMS-1; assist with evaluations and result documentation; maintain patient/sample databases; handle data queries; coordinate with study teams, sites and internal project management.

The Quality Assurance Intern will assist in developing and maintaining the Quality Management System, support QA activities, and participate in supplier qualification and audit preparation.

The Quality Assurance Associate ensures compliance with regulatory requirements, assists in maintaining the Quality Management System, and analyzes quality data trends to improve processes.