As a Bioinformatics Engineer at AccuScan Sciences, you will develop, optimize, and maintain bioinformatics pipelines utilizing AWS infrastructure and Nextflow workflow management systems. Your contributions will directly impact innovative scientific discoveries and product development. You'll collaborate closely with scientists, engineers, and researchers, contributing your technical expertise to streamline processes, maintain automation, and drive our bioinformatics capabilities forward.
Responsibilities:
Design, implement, and develop tests and documentation for established robust bioinformatics pipelines.Optimize computational workflows for high-performance execution and reproducible data analysis.Maintain, monitor, and improve pipeline automation to ensure smooth operational workflows.Manage GitHub repositories, oversee version control, and streamline the software release process.Develop and manage infrastructure on AWS to ensure scalability, reliability, and efficiency.Collaborate with cross-functional teams to integrate bioinformatics solutions.Proactively identify opportunities to enhance infrastructure efficiency and security.Requirements
Qualifications:
Bachelor’s degree or higher in Bioinformatics, Computational Biology, Computer Science, or a related field. with at least 3+ years of working experience out of college.Experience with bioinformatics workflow development and optimization, particularly using Nextflow.Experience developing software following best practices, including comprehensive testing and clear documentation.Proficiency in scripting languages (Python, Bash) and familiarity with container technologies (Docker, Kubernetes).Hands-on experience with AWS cloud computing services (EC2, S3, Batch, Lambda).Excellent communication and collaborative skills.Preferred Qualifications:
Familiarity with CI/CD practices.Experience with infrastructure-as-code (Terraform, CloudFormation).Benefits
Health Care Plan (Medical, Dental & Vision)Retirement Plan (401k, IRA)Paid Time Off (Vacation, Sick & Public Holidays) Read LessThe Head of Business Development will lead AccuScan's external growth strategy, strategic partnerships, and commercial business development activities. This executive will be responsible for identifying, negotiating, and executing partnerships with pharmaceutical companies, biotechnology companies, diagnostic firms, academic medical centers, health systems, and potential distribution partners.
The successful candidate will build and manage a robust deal pipeline while helping shape AccuScan's commercialization strategy for its MRD portfolio. This leader will play a key role in accelerating clinical adoption, expanding global market opportunities, and driving revenue growth.
Key Responsibilities
Strategic Business Development
Develop and execute AccuScan's business development strategy aligned with corporate objectives.Identify, prioritize, and secure strategic partnerships with pharma, biotech, diagnostics, reference laboratories, and health systems. Structure partnership opportunities from initial discussions through deal execution.Build and maintain a robust opportunity pipeline spanning research collaborations and commercial partnerships.Evaluate new market opportunities and adjacent growth areas that expand the AccuScan platform.Manage executive-level relationships with key external stakeholders.Coordinate cross-functional teams to ensure successful partner onboarding and execution.Collaborate with Product Management, R&D, Clinical Development, and Operations to refine go-to-market strategies.Requirements
Required
13+ years of business development, strategic partnerships, or commercial leadership experience in oncology diagnostics, molecular diagnostics, genomics, precision medicine, or life sciences.Demonstrated track record of sourcing, negotiating, and closing complex strategic partnerships.Deep network across pharmaceutical, biotechnology, and diagnostic companies.Strong understanding of oncology, companion diagnostics, MRD testing, and precision medicine markets.Experience leading cross-functional deal teams from opportunity identification through contract execution.Strong financial, commercial, and strategic analysis skills.Excellent executive communication and negotiation abilities.Preferred
Experience with MRD, liquid biopsy, NGS, or molecular diagnostic platforms.Experience supporting commercialization of LDTs, IVDs, or companion diagnostics.Understanding of reimbursement and evidence-generation strategies.Experience with global partnerships, including Europe and Asia.PhD, MD, MBA, or equivalent advanced degree preferred. Read LessThe Associate Director/Director of Clinical Product Development will lead end-to-end development and execution of clinical-stage molecular diagnostics. This role is responsible for translating scientific innovation into clinically validated, regulatory-ready, and commercially viable products, spanning assay development, clinical evidence generation, regulatory strategy, and market access.
This position plays a critical leadership role in advancing molecular diagnostic products from LDT development through clinical validation, MolDx reimbursement, and potential IVD/CE-IVDR pathways, supporting multi-indication oncology programs.
Key Responsibilities
Define and lead product development strategy aligned with clinical, regulatory, and commercial objectivesDrive development of end-to-end workflows (sample-to-report), including assay, bioinformatics pipeline, and operational scalabilityOversee development and optimization of clinical assays, including: Analytical performance (sensitivity, specificity, error modeling)Workflow scalability and automationOversee clinical validation studies, ensuring generation of data packages suitable for regulatory submissions and payer evidence requirementsSupport transition from research to CLIA/CAP LDT and future IVD/kit formatsEnsure product readiness for commercialization and operational scaleBuild and lead a high-performing clinical product development teamMentor team members and establish best practices for clinical product developmentRequirements
Education & Experience
PhD or equivalent in molecular biology, genetics, oncology, or related field10+ years of experience in diagnostics or biotech, with strong focus on clinical product developmentProven experience leading development of oncology diagnostics, preferably tumor tissue sequencing assays and/or ctDNA based assays for somatic mutation detectionExperience with tumor tissue sample processing from FFPE block, H&E staining, DNA extraction to sequencingDeep understanding of liquid biopsy, oncology diagnostics and NGS-based assay developmentFamiliarity with assay validation frameworks (CLIA/CAP, analytical validity, clinical validity, clinical utility)Demonstrated success in clinical validation and regulatory/reimbursement submissionsPrior experience with MRD detection approaches is a plus Read LessThe Scientist, Reagent Manufacturing & Quality Control (QC), is responsible for the production, characterization, and release testing of enzymes and critical reagents to support internal R&D activities and external diagnostic kit manufacturing, including in vitro diagnostic (IVD) products. This role is instrumental in ensuring that reagents meet performance, quality, and regulatory requirements.
The position is highly hands-on and requires execution of controlled manufacturing processes, analytical testing, and rigorous documentation practices to support design control, traceability, and regulatory compliance. The scientist will work cross-functionally to support assay development, verification/validation activities, and manufacturing readiness.
Key Responsibilities
IVD Reagent Manufacturing
Prepare and manufacture buffers and reagents under controlled processes to support IVD product development and commercial manufacturingExecute batch production with full traceability, including raw materials, lot tracking, and process documentationSupport scale-up and technology transfer activities for reagent manufacturingProtein Expression & Purification
Perform recombinant protein expression and purification using validated workflows Ensure batch-to-batch consistency and reproducibility of critical reagentsSupport process characterization and robustness studies required for design and validationQuality Control (QC) & Release Testing
Perform QC and release testing of enzymes and reagents against defined specifications Generate, review, and approve QC data packages to support lot releaseIdentify and investigate out-of-specification (OOS) or out-of-trend (OOT) resultsDesign Control & Validation Support
Support reagent characterization studies for design verification and validation (V&V)Contribute to defining reagent specifications, acceptance criteria, and stability protocolsAssist with preparation of technical documentation for regulatory submissions (e.g., CE-IVDR technical files)Documentation, Traceability & Regulatory Compliance
Maintain complete and accurate documentation in accordance with QMS requirements (e.g., ISO 13485, CE-IVDR)Ensure compliance with Good Manufacturing Practices (GMP) and controlled documentation systemsSupport deviation investigations, root cause analysis, CAPA, and change control processesContribute to audit readiness (internal, notified body, and regulatory inspections)Laboratory Operations & Equipment Management
Operate, maintain, and qualify laboratory equipment used in reagent manufacturing and QC testing Maintain calibration, maintenance, and equipment logs in compliance with QMS requirementsManage inventory of raw materials, critical reagents, and consumables with appropriate controlsCross-Functional Collaboration
Collaborate with assay development, clinical, regulatory, and manufacturing teams to ensure reagent performance meets product requirementsSupport integration of reagents into validated IVD workflowsParticipate in risk assessments (e.g., FMEA) related to reagent performance and manufacturing processesRequirements
Required Qualifications
B.S. or M.S. in Biochemistry, Molecular Biology, Protein Chemistry, or related field Minimum 3+ years of experience in reagent manufacturing, protein production, or QC testing in a regulated or semi-regulated environment Hands-on experience with protein expression and purification workflows Familiarity with analytical and QC methods (e.g., HPLC, qPCR, UV-Vis spectroscopy) Understanding of assay-critical reagent performance and variability driversWorking knowledge of documentation standards and quality systemsStrong attention to detail, data integrity, and traceabilityAbility to execute within a controlled quality system and follow SOPs strictly Strong problem-solving and troubleshooting capabilitiesEffective communication in cross-functional and regulated environments Familiarity with reagent stability studies and shelf-life determinationPreferred Qualifications
Experience in IVD product development, particularly under CE-IVDR or ISO 13485 environmentsExperience supporting design control, verification/validation (V&V), and technical documentationExperience with enzyme manufacturing for molecular diagnostics (e.g., NGS, PCR-based assays)Prior exposure to audits or regulatory inspections Read LessAccuScan Sciences is simultaneously executing multiple high-priority, interdependent programs across five workstreams. This level of operational complexity has exceeded the capacity of ad hoc or single-project management and now requires centralized program leadership to strengthen execution discipline, cross-functional coordination, and timeline accountability.
The Director, Program Management will provide centralized program and portfolio leadership to translate AccuScan’s strategy into executable plans, drive multi-workstream execution, and ensure leadership has timely visibility into milestones, risks, dependencies, resources, decisions, and progress. This role will establish the governance structure, operating cadence, and reporting discipline required to support OKR achievement and delivery against critical timelines.
KEY RESPONSIBILITIES
Requirements
QUALIFICATIONS
Required
MBA, PhD, or advanced degree in business, life sciences, genomics, diagnostics, engineering, healthcare administration, or a related field.Minimum 10 years of relevant experience in program management, portfolio management, product development, diagnostics, genomics, life sciences, clinical operations, laboratory operations, or regulated healthcare environments.Demonstrated experience in program or portfolio management within diagnostics, genomics, life sciences, or a related technical or regulated industry.Strong experience managing project managers, workstream leads, or cross-functional execution teams.Proven ability to drive multi-workstream execution across product, clinical, regulatory, business development, operations, quality, IT, commercial, and leadership stakeholders.Strong capability in end-to-end planning, milestone tracking, risk management, resource planning, and dependency management across complex programs.Experience establishing program governance, operating cadence, reporting structures, executive updates, decision forums, and escalation mechanisms.Excellent written and verbal communication skills, with the ability to synthesize complex issues into clear executive-level updates, recommendations, and decision requests.Proficiency with common project management and productivity tools such as Microsoft Office, Teams, Planner, SharePoint, Excel, PowerPoint, or equivalent systems.
Preferred:
COMPETENCIES
PHYSICAL DEMANDS AND WORK ENVIRONMENT
We are proud to be an equal opportunity employer committed to fostering an inclusive and diverse workplace. We welcome and encourage applicants from all backgrounds to apply. We do not discriminate on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, pregnancy, childbirth, or any other status protected by applicable federal, state, or local law. If you need an accommodation during the application process, please contact our Human Resources team.
Benefits
Read LessAccuScan Sciences is a biotechnology company developing whole-genome-sequencing-based liquid biopsy tests for minimal residual disease detection and precision oncology applications. Our work sits at the intersection of genomics and precision oncology, with a focus on advancing diagnostic capabilities that can help inform patient care and clinical decision-making.
As Project Manager, you will help drive cross-functional programs that support the development and operational readiness of complex diagnostic initiatives. This role plays an important part in keeping teams aligned around shared goals, maintaining momentum across interconnected workstreams, and supporting effective coordination among scientific, operational, regulatory, and quality-focused stakeholders.
ResponsibilitiesMaintain integrated project plans across cross-functional teams.Monitor deliverables and dependencies aligned to product objectives.Ensure adherence to development timelines and escalate risks as needed.Facilitate cross-functional project meetings and track action items.Manage the timeline for Clinical operations.Coordinate cross-functional activities required for inspection preparedness.Align laboratory operational readiness with accreditation and inspection timelines.Proactively identify project risks and mitigation strategies.Maintain clear communication across stakeholders.Serve as central point of coordination for project-level reporting.Requirements
Qualifications· Bachelor’s degree required; PMP or equivalent certification is a plus.
· 3+ years of project or program management experience in biotech, diagnostics, or life sciences
· Experience with cross-functional milestone tracking and coordinating cross-functional teams required.
· Experience working with laboratory operations, regulatory, and quality teams required.
· Eligibility to work in the United States required.
· Experience supporting clinical development programs in oncology or molecular diagnostics preferred.
Benefits
Read LessAccuScan Sciences is a liquid biopsy biotechnology company developing whole-genome sequencing solutions for minimal residual disease detection in oncology. The team is focused on turning complex clinical and genomic insights into products that can support more informed cancer care and broaden the impact of precision diagnostics.
In this role, you will shape product strategy for a growing oncology portfolio, helping connect scientific innovation, clinical evidence, and market needs. You will work across internal teams and external stakeholders to guide how products are defined, positioned, and advanced in regulated global markets.
ResponsibilitiesDefine the product roadmap for MRD assays across multiple indications.Translate clinical data into product requirements, claims, and market positioning.Support regulatory and reimbursement strategies, including work related to MolDx, IVDR, and PMDA.Drive global market strategy.Coordinate cross-functional execution from development through launch.Engage key opinion leaders, partners, and consortia to inform product direction.Requirements
8+ years of product management experience in oncology diagnostics or molecular diagnostics.Experience launching regulated IVD or LDT products across global markets.Strong knowledge of MRD and liquid biopsy, with experience in clinical evidence strategy.Experience working with MolDx, IVDR, and PMDA.Proven ability to interface effectively with key opinion leaders, commercial leadership, regulatory teams, reimbursement teams, and external partners.Must be eligible to work in the United States.A PhD or MBA is a plus. Read LessAccuScan Sciences is a biotechnology company developing whole-genome-sequencing-based liquid biopsy tests for minimal residual disease detection and precision oncology applications. Our work sits at the intersection of genomics and precision oncology, with a focus on advancing diagnostic capabilities that can help inform patient care and clinical decision-making.
As Project Manager, you will help drive cross-functional programs that support the development and operational readiness of complex diagnostic initiatives. This role plays an important part in keeping teams aligned around shared goals, maintaining momentum across interconnected workstreams, and supporting effective coordination among scientific, operational, regulatory, and quality-focused stakeholders.
ResponsibilitiesMaintain integrated project plans across cross-functional teams.Monitor deliverables and dependencies aligned to product objectives.Ensure adherence to development timelines and escalate risks as needed.Facilitate cross-functional project meetings and track action items.Manage the timeline for CLIA certification and CAP accreditation readiness.Coordinate cross-functional activities required for inspection preparedness.Align laboratory operational readiness with accreditation and inspection timelines.Proactively identify project risks and mitigation strategies.Maintain clear communication across stakeholders.Serve as central point of coordination for project-level reporting.Requirements
Qualifications· Bachelor’s degree required; PMP or equivalent certification is a plus.
· 3+ years of project or program management experience in biotech, diagnostics, or life sciences
· Experience with cross-functional milestone tracking and coordinating cross-functional teams required.
· Experience working with laboratory operations, regulatory, and quality teams required.
· Eligibility to work in the United States required.
· Experience supporting CLIA/CAP accreditation, LDT development, or regulated laboratory environments preferred.
· Experience supporting clinical development programs in oncology or molecular diagnostics preferred.
Benefits
Read LessPOSITION OVERVIEW
We are seeking a highly motivated Research Scientist to lead technology research efforts focused on the development of novel genetic and epigenetic molecular assays. This role offers an excellent opportunity for a hands-on molecular biologist to apply deep technical expertise in a dynamic, fast-growing biotechnology company.
The successful candidate will work closely with senior scientific staff and cross-functional R&D teams to drive experimental design, execution, and data interpretation in support of innovative assay development.
RESPONSIBILITIES
Under the guidance of senior scientific staff, propose, design, and execute experimental studies to advance new molecular assay technologiesAnalyze and interpret experimental data with strong scientific rigor and critical thinkingPrepare and present research findings to management and the broader R&D organizationCollaborate effectively with cross-functional R&D teams to support project execution and development timelinesMaintain accurate, detailed, and compliant experimental documentation through high-quality laboratory notebooks and data recordsManage multiple priorities with flexibility to meet time-sensitive project milestones and organizational objectivesStay current with scientific literature, emerging technologies, and advances in the fieldContribute to intellectual property development, including invention disclosures and patent filingsRequirements
QUALIFICATIONS
Ph.D. in Molecular Biology or a related field with 1–2 years of post-doctoral or industry experience, orBenefits
Health Care Plan (Medical, Dental & Vision)Retirement Plan (401k, IRA)Paid Time Off (Vacation, Sick & Public Holidays) Read LessAccuScan Sciences is seeking a dedicated Research Associate to join our innovative team. In this role, you will support various research projects focusing on assay development and clinical validation. You will assist in experimental design, data collection, and analysis while collaborating with scientists to advance our MRD assay.
Responsibilities:
Receive and process specimen shipmentsPrepare samples for routine testing and analysisConduct testing under supervision of a senior staffPerform routine technical procedures and functions according to departmental Standard Operating ProceduresContribute to molecular biology and genomics workflow development and improvementsEnsure accurate and consistent recording of experiment methods, materials and results; keep a high-quality laboratory notebookMonitor, operate and troubleshoot equipment to ensure proper functionality Maintain a clean, orderly, and safe lab environmentAssist with safety, hazardous waste, and facilitiesDemonstrate the ability to make technical decisions regarding testing and problem solvingPerform other duties as neededAdjust work schedule to meet time-sensitive project milestonesRequirements
Qualifications:
Bachelor’s degree in a life science or equivalentOne year of experience working in a lab settingKnowledge of basic laboratory safety and protocolSkilled in working with basic laboratory equipmentStrong understanding of standard molecular biology techniques (such as PCR, gel electrophoresis, and DNA/RNA isolation)Proficiency with basic computer skills, including data entry, spreadsheets, and document preparationPreferred Qualifications:
Experience in a research laboratory setting.Experience with next-generation sequencing (NGS) technologies.Benefits
Health Care Plan (Medical, Dental & Vision)Retirement Plan (401k, IRA)Paid Time Off (Vacation, Sick & Public Holidays) Read Less