Remote Jobs at GRAIL

- Bachelor's degree in science, engineering, or other technical area - Minimum of 5 years of experience working within a medical device, pharmaceutical, or biotech quality management system - Experience working with in vitro diagnostic medical device regulations and standards (e.g., ISO 13485, ISO 14971, 21 CFR 820, IVDR)

Candidates should possess a BS/BA degree, preferably in science, healthcare, or a related field, with an advanced degree in science, public health, or allied healthcare being strongly preferred. A minimum of 20 years of experience in partnership development and account management, focusing on substantive, revenue-generating accounts, is required. Additionally, 15 years of experience working with payer and policy executives is necessary, including deep knowledge of reimbursement pathways, system …

- Experience in clinical trial management, preferably in a fast-paced environment - Ability to work in ambiguity and proactively seek resources to solve problems - Proactive in seeking and utilizing resources to effectively solve problems - Ability to be flexible and creative in problem-solving - Ensuring clinical trials are executed within compliance of regulations and of the highest quality - Ability to identify areas of improvement to drive efficiency within Clinical Operations - Strong leade…

- Reside within the territory (Tucson, AZ, New Mexico, and El Paso, TX) - Field-based role requiring >85% time on in-person visits to targeted physician practices, planning/supporting events, and executing company initiatives - Market builder mindset with urgency and passion to engage physicians and staff, change cancer screening practices, and integrate MCED technology into workflows - Deep understanding of the Laboratory Developed Test (LDT) market, competitive landscape, and current cancer sc…

- Reside within the Charlotte/Raleigh, NC territory and surrounding areas - Ability to spend the majority of time (>85%) making in-person visits to targeted physician practices, planning and supporting events, and executing company initiatives - Market builder mindset with urgency and passion to engage physicians and staff - Deep understanding of the Laboratory Developed Test (LDT) market, competitive landscape, and current cancer screening options

- Bachelor of Science, or an equivalent combination of training and experience - Working knowledge of local, state, and federal laboratory regulations - At least three years of CAP/CLIA certified Laboratory Supervisory experience or equivalent - Exceptional understanding of CAP, CLIA and NYSDOH regulations - Strong communicator with ability to maintain open communication with internal employees, managers and customers as needed - Able to integrate and apply feedback in a professional manner - Ab…

- PhD in Life Sciences, Molecular Biology, Biochemistry, Bioengineering, or a related field - Proven experience in technology transfer of assays and launching new products in a regulated diagnostic laboratory - Direct, hands-on experience with end-to-end clinical workflows (pre-analytical, analytical, and post-analytical) - Strong knowledge of high-throughput laboratory automation and advanced instrumentation - Deep understanding of clinical laboratory regulatory standards, including CLIA, CAP, …

- Experience leading and implementing global audit management programs (internal, external, supplier) in compliance with QMS for product development lifecycle functions (e.g., manufacturing, clinical labs, supply chain) - Ability to interface with all organizational levels, conduct audits, report findings, and manage audit lifecycle to completion - Expertise in developing, managing, and executing inspection readiness programs, including logistics, SME training, mock inspections - Knowledge of ma…

- 15+ years of progressive People Partner experience

- Bachelor’s degree required; advanced degree preferred (MBA/MPH) - 8+ years total experience with 3+ in HCP/clinical marketing in diagnostics, biotech, or medtech - Primary Care and/or Oncology experience is a plus - Knowledge of lab-based diagnostic testing and lab-developed tests is a plus - Experience developing content and messaging for a clinical audience, including agency and creative talent management to execute - Proven ability to collaborate and work cross-functionally to drive results…

- Bachelor’s degree required; advanced degree strongly preferred (MS, MPH, PhD, PharmD, or MBA with strong scientific acumen) - 10+ years total experience with 5+ years in HCP/clinical marketing or Medical Affairs roles within diagnostics, biotech, or medtech; oncology or primary care experience a plus - Demonstrated leadership of national congress portfolios, KOL/peer-to-peer programs, and clinical content development in a regulated environment - Deep familiarity with MLR processes and claims g…

- B.S. / M.S. in a quantitative field (e.g., Computer Science, Engineering, Mathematics, Physics, Computational Biology) with 8+ years of related industry experience, or Ph.D. with at least 5 years of related industry experience or equivalent - Extensive experience developing with relational databases, data modeling principles, data pipeline tools, and workflow engines (e.g., SQL, DBT, Apache Airflow, AWS Glue, Spark) - Extensive experience with DevOps practices, including CI/CD pipelines, conta…

- BS/BA or equivalent in Engineering, Physics, Chemistry or Life Sciences with 2+ years of experience - Strong interpersonal, organizational, and troubleshooting skills

- Ability to work on-site from GRAIL’s Durham, NC facility approximately 3 days a week - Experience with Quality Management System (QMS) processes including CAPA investigations, NCR reporting, QMR, QMI, and Quality Indices - Knowledge of regulatory requirements including ISO 13485, ISO 14971, 21 CFR 820, IVDR, CAP/CLIA/NYSDOH, ISO 15189, and related standards - Strong critical thinking skills and good judgment to solve complex problems - Effective communication skills to report status and recomm…

- Minimum of 10 years of experience in regulatory, development, clinical affairs, quality, or program management within the IVD, medical device, or pharmaceutical industries - Regulatory affairs and IVD device experience preferred - An advanced degree may count toward years of experience - Direct experience with FDA regulatory submissions required - Experience with regulatory submissions in the EU, Japan, China, Canada