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Theradex Oncology

Full-service oncology CRO with regulatory support

Manager – Validation & Testing

Test Automation EngineeringUpdated on Nov 10
Full-timeRemote in USA$130k - $165k /yr

About the Job

Requirements

  • A bachelor's degree is required; an advanced degree is preferred.
  • At least 8 years of experience in Computer Systems Validation (CSV) and software testing.
  • At least 5 years of experience leading or managing validation, quality assurance, or testing teams.
  • Experience in pharmaceutical, biotechnology, contract research organization, medical device, or other regulated environments.
  • Demonstrated experience designing, implementing, and scaling automated testing frameworks.
  • Experience with relational databases, including SQL Server and Oracle.
  • Strong knowledge of GxP, GAMP 5, 21 CFR Part 11, and ALCOA+.
  • Knowledge of risk-based validation methodologies and a strong understanding of software development life cycle (SDLC) and Agile development methodologies.
  • Ability to understand system integration logic.
  • Ability to communicate technical and testing issues clearly with developers and stakeholders.
  • Ability to manage competing priorities in a fast-paced environment.
  • Strong analytical and problem-solving skills and attention to detail.
  • Ability to work independently and collaboratively in a remote setting.

Responsibilities

  • Lead the automation testing strategy for GxP and non-GxP systems, transitioning from manual testing to scalable, risk-based automated testing.
  • Evaluate, select, implement, and maintain tools and frameworks for functional, integration, regression, performance, application programming interface (API), data, and user acceptance testing.
  • Establish automation standards, coding practices, reusable test components, and test data approaches to improve consistency, coverage, and maintainability.
  • Integrate automated testing into software development life cycle (SDLC) and continuous integration/continuous delivery (CI/CD) processes to support reliable software releases.
  • Identify and prioritize automation opportunities based on business value, system risk, test frequency, and expected efficiency gains.
  • Define and monitor metrics for automation coverage, execution efficiency, defect detection, and test reliability.
  • Ensure automated test solutions used as GxP evidence are controlled, documented, versioned, reviewed, and able to produce complete and reliable execution evidence.
  • Lead risk-based validation for GxP applications, cloud platforms, databases, integrations, and reporting systems in accordance with regulations, industry guidance, and internal procedures.
  • Create, review, and approve validation deliverables, including validation plans, risk assessments, traceability matrices, installation qualification/operational qualification/performance qualification (IQ/OQ/PQ) protocols, test plans, test scripts, and validation summary reports.
  • Assess changes to determine validation impact and required testing for system enhancements and releases.
  • Manage validation deviations, root cause analyses, and corrective and preventive actions, as applicable.
  • Ensure validation and testing strategies address role-based access, segregation of duties, electronic records and signatures, audit-trail functionality, data integrity, and authorized review of audit information.
  • Maintain inspection and audit readiness and support internal, sponsor, and regulatory audits.
  • Oversee manual and automated functional, integration, regression, performance, security, data, and user acceptance testing for GxP and non-GxP systems.
  • Ensure test coverage is traceable to applicable business, functional, technical, quality, and regulatory requirements.
  • Review and approve test plans, scripts, evidence, results, and related validation documentation.
  • Establish testing templates, defect management practices, metrics, and reporting processes.
  • Partner with development and business teams to investigate defects, resolve issues, and support timely releases.
  • Lead, mentor, and develop validation and testing personnel, including training on CSV, GxP compliance, test automation, and quality practices.
  • Allocate resources, manage priorities, and oversee timely delivery of validation and testing activities.
  • Drive continuous improvement across validation, testing, and quality assurance processes while maintaining compliance requirements.
  • Develop and maintain validation, testing, SDLC, and related procedures and standards.
  • Ensure validation and testing records are complete, approved, consistently identified, retained in approved repositories, readily retrievable, and suitable to support inspections and audits.

About the Company

Theradex Oncology

Full-service oncology CRO with regulatory support

Theradex Oncology provides full-service contract research organization support for cancer trials across all indications and modalities, backed by MD oncologists, regulatory experts, and experienced operations teams. It runs trials from start-up to close-out by combining medical oversight, regulatory submissions, clinical monitoring, data management, and site operations. Its distinct advantage comes from deep oncology specialization, decades of hands-on experience with biotech and pharma sponsors, and a track record with NCI-supported studies. Its goal is to help sponsors conduct efficient, compliant trials and generate reliable data to advance new cancer therapies to patients.

Company size
51-200
Company stage
Not listed
Total funding
Not listed
Headquarters
Princeton, NJ
Founded
1982

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