Jobs at Discovery Life Sciences

Execute proteomics sample preparation and accessioning for platforms including Olink, Luminex, and mass spectrometry. Maintain reagent stocks, follow SOPs and safety procedures, document results, troubleshoot experiments with senior staff, and support multiple projects while developing independence and writing SOPs.

Support study candidate identification and data integrity by reviewing EMRs, performing data entry and reconciliation in Salesforce, scheduling tissue collection appointments, tracking data delivery deadlines, and sending shipment summaries. Role is onsite in Huntsville.

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.

Support development, validation, and execution of cell biology, immunology, and hematopoietic toxicity assays using human biospecimens. Perform cell culture, flow cytometry, ELISA, CFC assays, maintain lab records, troubleshoot protocols, and collaborate across multidisciplinary teams. Assist with SOP maintenance, sourcing materials, and presenting project updates.

Execute specimen logistics by collaborating with project managers and clinical sites to prioritize and ship samples, manage freezer farm and inventory, prepare and label shipments, follow SOPs and safety procedures, and support packing, receiving, and storage at specified temperatures.

Coordinate clinical site initiation, training, and biospecimen collection activities. Support monitoring visits, verify and maintain study documentation, track site performance, communicate between sites and internal teams, prepare reports, and help improve processes to ensure protocol compliance.

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.

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 laboratory operations by maintaining equipment qualification and documentation, coordinating calibration and service, managing inventory and reagents, supporting audits and CAPA, preparing routine solutions, coordinating proficiency testing, maintaining training records, and assisting continuous improvement of lab processes in a regulated environment.

Drive FP&A activities including complex financial modeling, revenue and pipeline valuation, budgeting and forecasting, variance and scenario analysis, CAPEX evaluation, and cross-functional financial business partnering to support strategic decisions and reporting to senior leadership.

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.

Coordinate flow cytometry lab operations: accession and track specimens using LIMS, manage inventory and shipments, perform basic equipment QC/calibration, support vendor service visits, and ensure regulatory and EHS compliance.

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

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.

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.

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.

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.