Abbott

Therapist

• Develop and maintain relationships with key physicians and site-specific stakeholders to achieve clinical trial enrollment objectives
• Streamline patient screening processes at participating sites
• Conduct referral and educational activities to support therapy development
• Define strategies to drive enrollment at clinical trial sites and meet enrollment targets
• Establish regular touchpoints with site investigators and research teams
• Elevate trial visibility and reinforce enrollment
• Support site teams with tools and best practices to qualify trial candidates
• Identify and address enrollment barriers
• Coordinate with cross-functional teams to ensure clinical site productivity
• Implement escalation plans for clinical trial sites
• Develop relationships with cardiologists, surgeons, and other key stakeholders
• Gather patient-pipeline data, track enrollment progress, and identify trends
• Facilitate clinical trial awareness activities and organize referral meetings
• Use analytical tools for referral activity planning
• Raise clinical trial awareness through newsletters, banners, and social media
• Coordinate communications to prioritize enrollment activities and support excellent procedural outcomes
• Maintain current product and clinical trial knowledge and participate in education programs
• Take evening and weekend calls occasionally for time-sensitive patient and customer needs

Senior Therapy Development Specialist

• Develop and maintain relationships with key physicians and site-specific stakeholders to achieve clinical trial enrollment objectives
• Streamline patient screening processes at participating sites
• Conduct referral and educational activities to support therapy development
• Define strategies to drive enrollment at clinical trial sites within the assigned territory
• Establish regular touchpoints with site investigators and research teams
• Support site teams with tools and best practices to qualify trial candidates
• Identify and address enrollment barriers and coordinate with cross-functional teams to ensure clinical site productivity
• Implement escalation plans for clinical trial sites
• Develop relationships with cardiologists, surgeons, and other key stakeholders
• Gather patient-pipeline data, track enrollment progress, and identify trends
• Organize referral meetings with general cardiologists and primary care physicians
• Use analytical tools for referral activity planning
• Raise clinical trial awareness through newsletters, banners, social media, and neighboring-hospital outreach
• Coordinate communications to prioritize enrollment activities and ensure excellent procedural outcomes
• Maintain current product and clinical trial knowledge and participate in education programs
• Perform occasional related duties, including evening and weekend calls for time-sensitive patient and customer needs
• Collaborate with the clinical study team, medical director, program and project management, clinical study personnel, commercial team, investigators, research coordinators, physician assistants, and nurses
• Execute responsibilities within corporate policies and standard operating procedures

Clinical Operations

• Independently create and maintain Clinical Evaluation Plans, Clinical Evaluation Reports, SSCPs, regulatory responses, and related documentation
• Identify, evaluate, and summarize clinical evidence from clinical investigations, literature, post-market surveillance, risk, and post-market clinical evaluations
• Analyze results for product applications and submissions
• Create, manage, or participate in deliverable timelines using project management tools
• Communicate timelines, project risks, and mitigation strategies with cross-functional teams and medical writers
• Interpret clinical, scientific, risk, and literature data for product applications
• Lead or support regulatory responses to Notified Body questions
• Facilitate document communication among Regulatory Affairs, R&D Engineering, Clinical Engineering, A&P, Marketing, Library Services, Quality Engineering, Post-market Surveillance, Clinical Affairs, Risk Management, Program Management, CROs, medical writers, and physician reviewers
• Provide strategic guidance on regulatory requirements related to clinical data and evaluations
• Support internal and external audits, audit responses, root cause analysis, corrective and preventive actions, effectiveness monitoring, and quality metrics
• Independently make decisions on CER-related regulatory issues
• Execute projects within budgetary guidelines

Senior Medical Writer / Senior Project Manager, Clinical Evaluation

• Create and maintain Clinical Evaluation Plans, Clinical Evaluation Reports, Summary of Safety and Clinical Performance documents, regulatory responses, and related documentation.
• Identify, evaluate, and summarize clinical evidence from clinical investigations, literature, post-market surveillance, risk, and post-market clinical evaluations.
• Analyze results for product applications and submissions.
• Create, manage, or participate in deliverable timelines using project management tools.
• Communicate timelines, project risks, and mitigation strategies with cross-functional teams and medical writers.
• Interpret clinical, scientific, risk, and literature data for product applications.
• Participate in or lead regulatory responses to Notified Body questions.
• Facilitate communication and document exchange among internal stakeholders and external vendors.
• Provide strategic guidance on regulatory requirements related to clinical data and evaluations.
• Support internal and external audits, audit responses, root cause analysis, corrective and preventive actions, effectiveness monitoring, and quality metrics.
• Act independently on CER-related regulatory issues.
• Execute projects within budgetary guidelines.

Technical Product Manager

• Own end-to-end technical product execution for a product/experience stream from concept through launch and continuous improvement
• Translate outcome-based strategy into epics, user stories, acceptance criteria, and release-ready backlog
• Define and maintain scope, decision rights, and accountability boundaries across teams
• Lead cross-functional operating cadence across Product, Commercial, Systems Engineering, Architecture, Program Management, and R&D
• Partner with Engineering and Architecture on technical trade-offs balancing speed, quality, compliance, and business value
• Co-own release readiness with the Program Manager, including dependency management, risk escalation, and launch quality
• Embed quality and compliance guardrails through shift-left testing, clear controls, and traceable decisions
• Drive stream-aligned delivery metrics and OKRs to improve predictability, throughput, and customer impact
• Support reusable platform and shared experience-service adoption with Platform & Delivery teams
• Maintain documentation and communication of technical product decisions and rationale
• Orchestrate alignment across the Products & Experience operating model and coordinate with Technical Leads, Architects, and Program Managers

Director, Technical Product Owner

Manager

• Lead planning and execution of complex EHR and system integration projects
• Manage project scope, schedule, requirements, issues, and risks
• Share project management best practices and identify process improvements
• Present integration progress, performance, and KPI reports to stakeholders
• Translate technical concepts for cross-functional audiences
• Establish and maintain relationships with internal and external stakeholders, including executives
• Evaluate emerging technologies, integration tools, and industry best practices
• Develop strategies and solutions for EHR interoperability and data exchange
• Provide advanced technical guidance on integration standards and practices
• Conceptualize, document, and present integration solutions to senior management
• Support the company Quality Management System
• Maintain regular and reliable attendance
• Travel between Exact Science locations and spend approximately 10% of working time traveling

Senior Integration Manager

• Lead the planning and execution of complex EHR and system integration projects, ensuring alignment with organizational goals and regulatory compliance
• Manage project scope, schedule, requirements, issues, and risks; share best practices and identify process improvements
• Present integration progress, performance, and KPI reports to stakeholders, translating technical concepts for cross-functional audiences
• Establish and maintain relationships with internal and external stakeholders, including executives
• Evaluate emerging technologies, integration tools, and industry best practices to enhance integration capabilities and scalability
• Evaluate technical process and concept recommendations using business strategy and performance considerations
• Develop strategies and solutions for system interoperability and data exchange between EHR platforms
• Provide advanced technical guidance on integration standards and practices to product development teams
• Conceptualize, document, and present integration solutions to senior management
• Uphold company mission and values and comply with Quality Management System policies and procedures
• Maintain regular and reliable attendance
• Act with an inclusion mindset and model inclusive behaviors

• Lead planning and execution of complex EHR and system integration projects
• Manage project scope, schedules, requirements, issues, and risks
• Share project management best practices and identify process improvement opportunities
• Present integration progress, performance, and KPI reports to stakeholders
• Translate technical concepts for cross-functional audiences
• Establish and maintain relationships with internal and external stakeholders, including executives
• Evaluate emerging technologies, integration tools, and industry best practices
• Evaluate technical process and concept recommendations using business strategy and performance knowledge
• Develop strategies and solutions for system interoperability and data exchange between EHR platforms
• Provide technical guidance on integration standards and practices to product development teams
• Conceptualize, document, and present integration solutions to senior management
• Support the company’s Quality Management System policies and procedures
• Uphold company mission and values and model an inclusion mindset
• Maintain regular and reliable attendance

• Lead planning and execution of complex EHR and system integration projects
• Manage project scope, schedule, requirements, issues, and risks
• Share project management best practices and identify process improvement opportunities
• Present integration progress, performance, and KPI reports to stakeholders
• Translate technical concepts for cross-functional audiences
• Establish and maintain relationships with internal and external stakeholders, including executives
• Evaluate emerging technologies, integration tools, and industry best practices
• Evaluate technical process and concept recommendations using business strategy and performance considerations
• Develop strategies and solutions for system interoperability and data exchange between EHR platforms
• Provide advanced technical guidance on integration standards and practices to product development teams
• Conceptualize, document, and present integration solutions to senior management
• Support company mission, values, and Quality Management System policies and procedures
• Maintain regular and reliable attendance
• Model an inclusion mindset
• Travel between Exact Science locations and travel up to 10% of working time

Medical Director

• Provide medical and scientific support for new product development from concept through commercialization
• Provide medical support to the Office of the Chief Medical Officer, including representation at medical conferences, sales meetings, and physician/hospital interactions
• Develop medical assessment documents, scientific reviews, medical opinions, and clinical evidence summaries
• Serve as a clinical subject matter expert on laboratory medicine, diagnostic testing practices, healthcare workflows, and customer needs
• Ensure clinical and medical requirements are incorporated into product design and design-control activities
• Evaluate clinical risks and provide recommendations for safe and effective product development
• Participate in medical oversight for product performance, post-market surveillance, and patient safety
• Review product complaints, Medical Device Reports (MDRs), adverse-event trends, and other post-market data
• Conduct or support Health Hazard Evaluations (HHEs), medical risk assessments, and benefit-risk analyses
• Partner with Quality and Regulatory Affairs to investigate product performance issues and determine corrective actions
• Strengthen medical risk-management and product-safety monitoring processes
• Provide medical input into clinical study design, protocol development, and clinical risk mitigation
• Review clinical data and product performance information for regulatory submissions and post-market activities
• Support interactions with the FDA and international health authorities
• Support compliance with global regulations, quality standards, and medical-device reporting requirements
• Recommend enhancements to product monitoring, safety assessments, and risk-evaluation methodologies
• Assess the clinical significance and patient, provider, and laboratory impact of product-performance findings
• Present medical assessments, risk evaluations, and scientific recommendations to leadership and cross-functional stakeholders
• Represent Medical Affairs at scientific meetings, customer interactions, physician engagements, industry conferences, and internal business meetings

Associate Medical Director, Medical Affairs

General

• Provide primary support to ADD customers and field personnel for complex instruments, including onsite integration, assay training, and troubleshooting
• Resolve instrument and reagent issues onsite and remotely, documenting information in the complaint handling system
• Lead complex instrument and reagent integrations at customer sites
• Collaborate with project managers to execute technical plans
• Conduct entrance interviews, assess customer needs, and manage expectations
• Plan and oversee integration processes
• Provide onsite operations training to customers
• Manage integration timelines and conduct exit interviews
• Deliver onsite and remote technical support for hardware, software, and reagent issues
• Troubleshoot performance concerns to improve customer self-sufficiency
• Document complaints and resolutions in the CAPA system
• Identify product and process gaps to support continuous improvement
• Act as a Subject Matter Expert for internal teams
• Provide feedback on product performance and customer usability
• Support account management in critical situations
• Maintain technical proficiency and follow work processes, safety guidelines, and documentation standards
• Manage projects, time, and customer accounts in line with organizational priorities and sales objectives
• Influence customer satisfaction in a high-visibility role
• Operate independently and collaborate across teams and functions
• Drive CAPA effectiveness through accurate documentation and resolution of customer concerns
• Uphold integrity and transparency in customer and internal interactions

Technical Applications Specialist, East Region

• Provide primary support to ADD customers and field personnel for complex instruments, focusing on onsite integration, assay training, and troubleshooting
• Resolve instrument and reagent issues onsite and remotely, documenting information in the complaint handling system
• Lead complex instrument and reagent integrations at customer sites with project managers
• Conduct entrance interviews, assess customer needs, and manage expectations
• Plan and oversee integration processes
• Provide onsite operations training to customers
• Manage integration timelines and conduct exit interviews to present results and secure customer buy-in
• Deliver onsite and remote technical support for hardware, software, and reagent issues
• Troubleshoot performance concerns to improve customer self-sufficiency
• Document complaints and resolutions in the CAPA system
• Identify product and process gaps to support continuous improvement
• Act as a subject matter expert for internal teams and influence sales, service, and support strategies
• Provide feedback on product performance and customer usability to drive design improvements
• Support account management in critical situations across sales and service teams
• Maintain technical proficiency and follow work processes, safety guidelines, and documentation standards
• Manage projects, time, and customer accounts in alignment with organizational priorities and sales objectives
• Operate independently with broad discretion and collaborate across teams and functions
• Drive CAPA effectiveness through accurate documentation and resolution of customer concerns
• Uphold integrity and transparency in customer and internal interactions

Technical Applications Specialist – East Region

Clinical Specialist

• Provide advanced engineering, sales, educational, and technical support for complex EP product inquiries
• Act as a senior clinical interface between the medical community and the business
• Build and sustain credible business relationships with customers
• Identify and report customer needs, product performance, and sales opportunities
• Provide engineering, sales, education, and clinical support for complex field inquiries
• Maintain thorough knowledge of EP products, related technical knowledge, trends, and competitors
• Develop, lead, and facilitate EP product trainings and programs for healthcare professionals
• Provide market feedback and guidance on next-generation products
• Provide regional EP procedural case coverage
• Back up EP Sales Representatives with sales support, training seminars, clinical studies/data collection, troubleshooting, and new product in-service training
• Mentor and provide leadership for less experienced Clinical Specialists
• Develop engineering, sales, and technical skills related to Arrhythmia Management strategy
• Assist Training and Education with advanced seminars and educational materials
• Assist Sales with advanced product demonstrations
• Stay current on technical developments, regulatory requirements, company and competitor products, markets, objectives, and industry trends
• Resolve problems and help prevent recurrence
• Monitor performance and report status to the manager
• Perform related assigned responsibilities

Senior Clinical Specialist

• Provide advanced engineering, sales, educational, and technical support for complex EP product inquiries
• Serve as a senior clinical interface between the medical community and the business
• Build and sustain credible business relationships with customers
• Identify and report customer needs, product performance, and sales opportunities
• Provide complex field inquiries support and maintain thorough knowledge of EP products, technologies, trends, and competitors
• Develop, lead, and facilitate trainings and programs on EP products for healthcare professionals
• Provide market insight and feedback for next-generation products
• Provide regional EP procedural case coverage
• Back up EP Sales Representatives with sales support, regional training, clinical studies/data collection, troubleshooting, and new-product in-service training
• Mentor and provide leadership for less experienced Clinical Specialists
• Develop engineering, sales, and technical skills related to Arrhythmia Management
• Assist Training and Education with advanced seminars and educational materials
• Assist Sales with advanced product demonstrations
• Remain current on expertise areas, regulatory requirements, company and competitor products, markets, objectives, and industry trends
• Resolve problems and facilitate prevention of recurrence
• Perform related assigned responsibilities

• Provide technical, clinical, and programming assistance primarily in support of 1–2 Territory Managers
• Assist Territory Managers with after-hours call support and activities
• Integrate into accounts, build trust and relationships, and establish strong customer rapport
• Provide complex programming and case support
• Conduct PCP work and educational in-services as directed
• Contact, visit, and engage clients and potential clients regarding company products
• Address client questions and concerns
• Provide medical professionals with sales support, product information, training, staff education, in-services, and technical troubleshooting
• Develop and maintain in-depth knowledge of assigned accounts, customers, and competitor activity
• Evaluate and develop sales strategies for capital equipment opportunities
• Collect and study information about new and existing products and monitor competitor sales, prices, and products
• Provide operating-room and non-operating-room guidance on directions for use of implantable devices
• Attend trade shows and conferences as needed
• Identify customer training and in-service needs to increase usage, comfort, and understanding of Abbott Chronic Pain Therapies
• Comply with FDA regulations, regulatory requirements, company policies, operating procedures, processes, and task assignments
• Maintain positive and cooperative communication and collaboration with employees, customers, contractors, and vendors
• Travel 25% within or outside the assigned region
• Perform other related duties as assigned

Senior Therapy Development Specialist

Senior Therapy Development Specialist

Senior Medical Writer / Senior Project Manager, Clinical Evaluation

Senior Medical Writer / Senior Project Manager, Clinical Evaluation

Director, Technical Product Owner

Senior Integration Manager

Senior Integration Manager

Senior Integration Manager

Senior Integration Manager

Associate Medical Director, Medical Affairs

Technical Applications Specialist, East Region

Technical Applications Specialist – East Region

Senior Clinical Specialist

Senior Clinical Specialist

Clinical Specialist I, CPT