The Senior Biobank Technician is responsible for the overall coordination, regulatory compliance, quality control, and data management of Biorepository Operations supporting Research Operations in the Phoenix, Arizona Lab.  This position will be responsible for supervising laboratory staff as well as conducting initial processing of blood and plasma samples.

The Customer Care Associate provides world class service to health care providers, patients and the general public. The Customer Care Associate will primarily receive inbound calls and place outbound calls as needed to health care providers, patients and other clients.         Video Credit: TheMuse.com. To view more of our content on the Muse, click here.

As a Senior QA Engineer I - Apttus, you will play a key role in defining, developing, refining, executing quality standards and design controls to successfully deliver business-critical SFDC/Apttus solutions as well as an integration of these systems with partners. You will be a part of the Apttus team supporting our Contract Lifecycle Management and Contract Pricing Module running on Salesforce.com from conception to going live with an emphasis on software quality for exceptional customer experience.You will be responsible for partnering with the Contract Lifecycle Management Product Owner, Development, System Analyst and other stakeholders in the continuous building, expansion, and customization of the CLM/CPM platforms within the Salesforce.com solution.

The Manager, Specimen Processing manages the Specimen Processing department at the Exact Sciences Laboratories. This position is responsible for overseeing the processes related to technology transfer of new assays, new sample types or assay improvements, which may include, but it not limited to, the general supervision and development of all aspects of implementation, space planning, coordination of cross-functional resources (e.g., IT), the development of processes, procedures, and training of laboratory staff while assuring that quality standards are being met consistently, and processes and systems are consistently emulated across all sites. This individual provides expertise and mentoring to laboratory staff and serves as the liaison to internal and external entities, including Exact Sciences Corporate and vendor relationships.  This position is also responsible for incorporating and being part of the oversight group for the sample management system.  The Manager, Specimen Processing will assist with the design, maintenance, and implementation of the Quality Management System (QMS) programs across the Lab and ensures the laboratory and the staff are in compliance with all laws and regulations required by CLIA, CAP, OSHA, CMS, and any other applicable legislative organizations.   The hours for this position are Monday - Friday from 2pm - 10:30pm. 

Through hands-on experience as well as observational and mentorship activities, the IT Intern will have the opportunity to learn about several aspects of Information Technology, Biotechnology and working in a real business environment.  Primary responsibilities will be to provide support services to Exact Sciences employees; primarily in the Madison locations, but remote support for geographically diverse employees.

The Supervisor, Production will supervise, lead, train, and assist a team in reagent manufacturing, dispensing using manual or automated processes, and packaging of final product.  This position will assist in developing and documenting new procedures for Production, as well as updating work instructions and processes streamlining the overall production.  This position will be responsible for equipping, staffing, and establishing systems for operations functions working closely with Production leadership and coordinating efforts. This is a first shift position with the potential for a modified shift in the future to accommodate business growth.   We are offering a $10,000 sign on bonus to new hires for this role. 

The Lead Production Associate requires a variety of skills necessary for Production Operations activities. This role will lead a variety of Production functions, including reagent production, process development, characterization, and validation. The position will work within defined protocols and procedures and may develop and document new procedures for Production. The Lead Production Associate is expected to possess a thorough understanding of laboratory procedures and conduct work within cGMP guidelines.   We are offering a $5,000 sign on bonus to new hires for this role. 

The Medical Education and Grants Specialist develops content, both delivered to and received by a variety of audiences; including healthcare professionals, quality, Market Access and population health experts, researchers, and patients to inform, educate, and elevate disease state and product awareness. This role is responsible for providing direct support to the development and management, from concept to execution, of the company’s Medical Education initiatives with a focus on development of medical materials to support Medical Education efforts. This role liaises with all commercial functions, with a strong and focused partnership on education of clinical and real-world data and Evidence Communications. Medical Education is a core function of the Medical Affairs department.

This position will be part of the Clinical Affairs Team, which is responsible for executing, managing and conducting projects associated with the company clinical study plans.  The Sr. CRA is responsible for site management deliverables on assigned protocols. With minimal supervision, the Sr. CRA manages the clinical monitoring activities of the study and assures site compliance with study protocols and applicable regulations and assists the Clinical Study Manager with study related activities, as required. The Sr. CRA may act as a lead CRA for the Sponsor.   This position will be remote and may be located anywhere in the United States.

The Lead Certified Clinical Laboratory Scientist provides leadership support to the technical lab staff. This person is also responsible for being the workflow and troubleshooting point person in the technical lab.  This position is primarily responsible for coordinating and conducting day-to-day activities in the laboratory to ensure timely and accurate testing. The Lead Certified Clinical Laboratory Scientist works directly with the Clinical Laboratory Supervisor to anticipate and resolve issues related to efficiencies in throughput, staffing, and laboratory processes. This position is also responsible for verifying result release and pending list management and investigation. The Lead is expected to spend at approximately half of their time performing laboratory testing on the bench.

The Integrations Program Administration Manager will drive continuity across multiple integrations as Exact Sciences continues to add products, technologies, and businesses to its infrastructure. This position will provide tactical, project, and program management support for the execution of integration strategies during the closing and integration phases of mergers, acquisitions, commercial partnerships, and technology-based deals. A successful candidate will have a high level of organization, attention to detail, and be able to work collaboratively across all levels of the organization to manage the complexity of integration-based activities.

The Bioinformatics Scientist II is a creative person who will conduct the development of data mining algorithms and tools using proprietary data and databases for scientific research and cancer biomarker discovery. The position offers exciting opportunity and significant growth potential within an innovative and dynamic genomic diagnostics company. The candidate should be experienced with next-generation sequencing data analysis, algorithm development, and bioinformatics programming with Python. Strong computational, mathematical, logical skills, and proven project experience with large genomic datasets are essential.  This position will interact with the teams in the R&D, Information Technology, and Clinical departments. Good oral and written communication skills are required.

We are looking for an experienced Privacy professional to join the Exact Sciences Privacy Office to partner with the laboratory and commercial business to embed privacy-by-design while creating policies and procedures to mitigate privacy risk. You'll work across marketing, technology, innovation, and R&D, to mention a few, to drive enterprise privacy initiatives, help create privacy-focused culture, educate stakeholders on why privacy matters, and how we can use data in an ethical way to build trust with our patients and consumers.   This position can be located in our Redwood City, CA office or remote. 

The Senior Research Associate I, with some guidance from more experienced scientists, works on projects which are moderate to complex in scope. The Senior Research Associate I participates in planning of projects and experiments and is responsible for the execution of experiments and analysis of data.  Working in a team setting, the Senior Research Associate I will primarily be involved in Research and Development projects actively participating in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products.   This Sr. Research Associate I will help to explore new technologies, ideas and concepts in application of early cancer detection.

The Client Services Representative will provide best-in-class service to internal and external clients of Paradigm Dx. Work with a wide variety of external parties to educate them on the product and assist in the ordering process, including oncologists, nursing staff, pathology departments, and patients. Ensure that all activities are performed within confines of CAP/CLIA/HIPAA regulations and guidelines for patient safety and protection. This is a one year, onsite opportunity.   https://www.linkedin.com/in/jennastoltz/

The Senior Research Associate I, with some guidance from more experienced scientists, works on projects which are moderate to complex in scope. The Senior Research Associate I participates in planning of projects and experiments and is responsible for the execution of experiments and analysis of data.  Working in a team setting, the Senior Research Associate I will primarily be involved in Research and Development projects actively participating in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products.

 The Staff Accountant position is responsible for maintaining general ledger accounts and business transactions of the organization, applying Generally Accepted Accounting Principles (GAAP). This includes creating financial transactions and creating financial reports from that information. This includes evaluating transactions for proper classification and making decisions regarding the posting of the transactions. The Staff Accountant also reconciles accounts to ensure their accuracy. In addition, the Staff Accountant assists with establishing policies and procedures for financial reporting and helps maintain the Company’s Sarbanes-Oxley (SOX) 404 compliance.

The Associate Director, Health Systems Operations is responsible for leading the Sales Excellence function to support the success of the health systems priorities and initiatives. This role will develop the support strategy and ensure successful implementation of processes, systems, and initiatives to meet business objectives. This role will work cross-functionally to identify best practices, solutions, and alignment with strategic initiatives.

The Senior HRIS Analyst will support our HR Systems primarily, but not limited to, Workday (Human Capital Management). A key responsibility of this role is to develop and continuously improve HR system processes to increase user adoption, ensure compliance with policy and regulations, and improve business performance.   This role will work closely with the Human Resources and Payroll teams to continually enhance and support HCM systems and processes. General working knowledge of all HR disciplines (Benefits, Recruiting, Compensation, Learning, Talent, and HR Self-Service) is critical to success in this role.   As part of the HR team, this role will collaborate regularly with team colleagues, HR stakeholders, and other business partners to ensure that business processes are optimized to align with the technology and provide an excellent user experience with the systems supported.   The Senior Analyst – Workday Security will be an important part of our Workday ecosystem team. This position will be responsible for evolving the security architecture and configuration. This role is critical to maintaining the scalability, efficiency, and accessibility of our system for all user groups globally. The role will be focused heavily on supporting the changes that will come during the evaluation phases of changing or updating our system and adding new functionality, as well as troubleshooting and any required security reporting.

The Associate Lead, Laboratory Processing (known internally as Laboratory Processing Workflow Coorinator) performs the functions of Specimen Processing under the guided direction of the Specimen Processing Supervisor, Lead or designee.  The Specimen Processing Workflow Coordinator follows laboratory policies and procedures and maintains accurate data reporting practices to ensure consistent and diligent execution of specimen processing. In this support position the Specimen Processing Workflow Coordinator ensures daily lab operations are effective and efficient by providing direction and guidance to employees during their assigned duty station.   The hours for this position are Tuesday - Friday from 6:00am - 4:30pm.