Clinical Operations Jobs in Pharma & Biotech

The Environmental, Health, and Safety (EHS) Document Control Coordinator will be responsible for the tracking, organization, and storage of all EHS compliance program documentation. This includes a wide variety of evidence of compliance documentation. Job Responsibilities Organization of the online and hard copies of company compliance documentation directly related to environmental, health and, safety regulations. Responsible for the EHS documentation control for multiple job sites company wide. Responsible for ensuring records are accurately retained in an efficient and timely matter as required to ensure quality and integrity of the data. Responsible in part, under the direction of EHS leadership for...

Clinical Associate In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. What You’ll Work On Working under general direction, provides engineering, sales, educational and technical support in response to field inquiries from physicians, health care professionals, patients, and field sales staff, involving EP products. Performs work that involves a high degree of independence. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Exercises...

POSITION SUMMARY The Clinical Project Specialist is responsible for assisting with and/or completing projects related to the GC team and/or the clinical aspects of Natera products. PRIMARY RESPONSIBILITIES Assist in the development of patient consents, GC protocols, SOPs, GC note templates, patient education materials. Write or collaborate on abstracts or papers involving Natera tests. Deliver presentations/posters at scientific meetings and company promotional events as needed; represent company at trade shows and medical conferences (<10% travel). This role works with PHI on a regular basis both in paper and electronic form and has access to various technologies to access PHI...

Help us change lives At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others. Position Overview The Lead Clinical Laboratory Scientist provides leadership support to the technical lab staff. This role is responsible for being the workflow and troubleshooting point person in the technical lab, coordinating and conducting day-to-day activities in the laboratory to...

Help us change lives At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others. Position Overview The Genetic Testing Coordinator I is responsible for coordinating testing and communication between departments. The Genetic Testing Coordinator I will assist with the entire inventory of active tests throughout the testing process. The schedule will be Monday-Friday, 12pm-830pm,...

Per Template The CoreValve Principal Therapy Development Specialist (TDS) provides technical, clinical, educational and sales support to ensure safe adoption and growth of the Medtronic CoreValve System and future catheter-based therapy technologies. The CoreValve Therapy Development Specialist works closely with implanting teams and the Medtronic Catheter-Based Therapies (CBT) and CVG field organizations to drive procedural and practice success. Technical and Clinical Expertise Provide clinical expertise for TAVR implanting centers, including “scrubbing in” for TAVI implant procedures to assist with loading valves onto delivery catheter, and providing technical support in accordance with the instructions for use/trial protocol, and best -practices...

A Clinical Trial Specialist provides operational and regulatory support for the Caris sponsored studies and collaborative Pharma studies ensuring activities are conducted per standard operating procedures and best practice principals. Responsibilities will include, but not limited to, study documentation maintenance, IRB submissions, leading site onboarding activities, driving site engagement through routine status meetings/ touch points, study enrollment/ accrual reporting, specimen tracking, accessioning, and inventory. Job Responsibilities Successfully execute site onboarding process in an effective and timely manner Develop and maintain a thorough understanding of study content, workflows, and procedures to successfully conduct the Site Initiation Visit meeting and offer ongoing...

This position works out of our St. Paul, MN location with our Regulatory Affairs team in the Structural Heart division. As an individual contributor, the function of a Regulatory Affairs Coordinator is to provide administrative support for regulatory processes and procedures. The individual may coordinate and support technical and scientific regulatory activities, research regulations and guidance, and organize and m aintain key information sources. The individual may also coordinate departmental activities, including budget tracking, office arrangements, and team events. Main Responsibilities Track departmental budget sheets, ensure alignment with invoices and payments, and monitor budget spending status. Handles invoice , cover...

Career Category Clinical The Cardiovascular/Metabolic Therapeutic Area is seeking a Clinical Research Medical Director to play a leadership role on one or more studies within the maridebart cafraglutide (AMG 133) global development program in obesity and related metabolic diseases. The position is located in Thousand Oaks, California, but depending on the situation a remote work arrangement will be considered. The role will report directly to the Global Development Lead for the AMG 133 program. Responsibilities Provide clinical/scientific knowledge into the development, design, execution and communication of the global evidence generation plan for the maridebart cafraglutide (AMG 133) phase...

This position works out of our Temecula, CA location in the Abbott Vascular division. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for the treatment of vascular disease. The Project Coordinator will Coordinate projects relating to, but not limited to, divisional labeling for international countries for the Product Lifecycle and Program Management (PLPM) group. What You’ll Work On Design, communicate, and implement an operational plan for completing the project. Monitor progress and performance against the project plan. Take action to resolve operational problems and minimize delays. Identify, develop, and gather the resources to complete the project. This may include...

This position, Project Coordinator, will work out of our San Diego, CA (La Jolla area) location in the Infectious Diseases group in Abbott Rapid Diagnostics. Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe. The crucial information derived from our tests, instruments, and informatics systems is often the first step in patient care decision-making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers. As a Project Coordinator you will Assist Development Assist in the development and implementation of company products and services, coordinating with departmental and cross-functional teams. Estimate...

Biogen’s West Coast Hub, based in South San Francisco, is specifically focused on transforming the lives of patients with severe immune-mediated diseases by developing novel targeted therapies with outsized clinical impact, faster. To accomplish this, we are seeking top talent to join us on our journey. We are seeking a Senior Clinical Trial Specialist (CTS) to assist in the execution of Clinical Trials. The successful candidate will be able to support the conduct of clinical trials with minimal guidance/supervision while ensuring alignment with GCP and Biogen's SOPs. The Specialist provides a high level of administration, coordination and organizational support to...

The Quality Control Scheduler/Coordinator role supports the clinical and commercial Quality Control testing groups associated with internal cell and genetic therapy manufacturing. This role is responsible for developing, monitoring, and maintaining QC testing schedules associated with development, in-process, release, and stability testing of internal manufacturing and process development activities. Key Duties and Responsibilities Builds and Maintains QC Schedules including, but not limited to, routine testing, instrument maintenance, laboratory readiness, and validation activities Collaborates within QC and across functions with key stakeholders such as Manufacturing, PD, and Facilities to integrate testing schedules with overall productions plans. Build and lead KPI dashboards/...

This role is a new 3rd shift team. This team will TRAIN on 2nd shift ( 345pm - 215am M-Th - 10h). Once trained, likely 1Q26, the team will move to 3rd shift (11pm - 730am M-F 8 hr day). Accountabilities · Coordinate packaging activities for all products as assigned · Work closely with the Process Facilitator to ensure department priorities are met · Understand and follow GMP procedures required to package product to specification · Assign packaging operators to predetermined visual staffing plan · Understand the daily packaging schedule to maintain line operation and adjust schedule if required ·...

Purpose We are devoted to discovering and developing new medicines for those patients with unmet medical needs. AbbVie's clinical research operates with a collaborative model that seeks to build the pipeline of discoveries from inside and outside the company's own walls. AbbVie's current therapeutic areas of interest are Antiviral (HCV, HIV and RSV), Immunology, Men's Health, Neuroscience, Oncology, Pain, Renal, and Women’s Health. Within each of these therapeutic areas, we have various products in development. The products will change over time as compounds progress through our development program. A critical component of medicinal product development is clinical research, which involves...

Clinical Associate In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. What You’ll Work On Working under general direction, provides engineering, sales, educational and technical support in response to field inquiries from physicians, health care professionals, patients, and field sales staff, involving EP products. Performs work that involves a high degree of independence. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Exercises...

Operations Support Complaint Coordinator The position of Operations Support Complaint Coordinator is within our Toxicology unit located in Portsmouth, Virginia at Instant Technologies. In this role, you will maintain accurate service issue (complaint) records to include, logging, escalating to the responsible Department Manager/Designee for investigation, routing to finance for crediting or inventory corrections, and for orchestrating any requests and follow up actions needed such as courier claims/tracers. You will also be the main source for communications (internally and externally) relating to service issues, RMA’s, courier returns, and shall ensure service issue records are accurately submitted for final review within...

This position works out of our Alameda, CA location in the Diabetes Care division where we are focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology. As a Coordinator Project Design, you will have the opportunity to provide organizational and project support to the department by working directly with a cross-functional teams, external translation suppliers, as well as internal Design Production Artists to coordinate and execute activities related to the development of packaging and labeling...

Contributes to program and study-level feasibility and operational parameters Via gathering and reviewing of evidence, uses, and contributes to project program/study milestones, create site selection criteria, and establish need for patient recruitment and retention strategies and tactics. Collaborates with senior Global Technical Operations staff, CSSM to align on deliverables. (25%) Contributes to program and study-level recruitment and retention plan initiates study-level assessment of patient recruitment needs and considers outreach and recruitment vendor strategies, in collaboration with senior Global Technical Operations staff. May contribute to implementation plans for delivery of recruitment and retention strategies and tactics in compliance with...

Impact patient outcomes. Come for a job, stay for a career. We seek out and hire a diverse workforce at every level We need fresh ideas and inclusive insights to continue to be an innovative industry leader — that’s why we make it a point to seek out, attract and develop employees who are patient-centric, passionate, and who represent the same wide variety of life experiences as our patients. As a DHF (Design History File) Technical Project Coordinator IV, you will develop life-saving medical device products for spine surgery in a fast-paced environment. Key responsibilities include providing project support...

POSITION SUMMARY The Multiple Primary Coordinators (MPC) will oversee the day to day operations of the multiple primary project. This senior level support position will consistently work on complex assignments and perform administrative duties such as coordinating care teams for patients, and acting as a liaison between Natera, patients, patient families, and health care professionals. The MPC will also develop and implement processes and author standard operating procedures related to the MP project. PRIMARY RESPONSIBILITIES Monitors daily operations and resolves sample processing issues to ensure timely and accuracy of information in order to maintain SLA for results. Performs complex assignments...

Multiple Primaries Coordinator - Weekend Coverage POSITION SUMMARY The Multiple Primary Coordinators (MPC) will oversee the day to day operations of the multiple primary project. This senior level support position will consistently work on complex assignments and perform administrative duties such as coordinating care teams for patients, and acting as a liaison between Natera, patients, patient families, and health care professionals. The MPC will also develop and implement processes and author standard operating procedures related to the MP project. PRIMARY RESPONSIBILITIES Monitors daily operations and resolves sample processing issues to ensure timely and accuracy of information in order to...

Clinical Associate In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. What You’ll Work On Working under general direction, provides engineering, sales, educational and technical support in response to field inquiries from physicians, health care professionals, patients, and field sales staff, involving EP products. Performs work that involves a high degree of independence. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Exercises...

This position works out of our Roseville, MN, location in the Electrophysiology division. In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. The Coordinator I, Quality Records position is responsible for organizing and managing records that are submitted to the Records Management department for the Roseville Distribution Center. Tasks include facility-wide records coordination, storage, preservation, and disposition of records according to legal and regulatory requirements. Position is to hire full time employee. Job Duties Prepare physical records for...

The responsibilities for this position may include, but are not limited to WAREHOUSE OPERATIONS Coordinate the receiving and delivery of research materials management (e.g. gSupply, MPLS, Sample, and gPackage), support managing the warehouses and MatOps programs. Support daily operations from the Centralized Service Command Center, gSupply/MPLS warehouse/labs to provide customer service, prioritizing delivery orders Receive the packages by operating the automated conveyor line, coordinate the staging of inbound/outbound materials, transport via fleet vehicles, and maintain inventory stock levels Promote an atmosphere of teamwork and cooperation by assisting the leads and supervisors in recognizing potential conflicts and offering help to a...

Help us change lives At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others. Position Overview The Clinical Lab Associate I, Specimen Processing is responsible for performing the day-to-day operations of the Specimen Processing Department including, but not limited to, lab productivity and process line support, such as accessioning, processing, automation usage, sample racking,...

This position works out of our Alameda, CA location in the Abbott Diabetes Care Division, where we are focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology. The CRA II will assist in the clinical execution and management of all aspects of assigned clinical studies. This includes but not limited to planning and implementation of clinical studies from concept to clinical study report per timelines and quality standards. This is an on-site, 5 days a...

This position works out of our Alameda, CA location in the Diabetes Care division where we are focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology. As a Coordinator Project Design, you will have the opportunity to provide organizational and project support to the department by working directly with a cross-functional teams, external translation suppliers, as well as internal Design Production Artists to coordinate and execute activities related to the development of packaging and labeling...

We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. The Logistics Coordinator position is responsible for providing operational and administrative support to both to the Logistics Operations shop floor, and Manager, Logistics Operations. The position plays a critical role in the daily/weekly activity planning, shipment processing and shipment status documentation and communication. The role works closely with the International...

POSITION SUMMARY The Human Resources Coordinator is responsible for a combination of routine and non-routine technical and administrative HR work. Performs some level of emerging professional HR responsibilities. Has a professional understanding of the HR discipline but limited authority to execute independently. Typically work as part of a team and operate under direct supervision. Supports multiple HR practices primarily by providing administrative duties that can range from employee data entry and validation, filing and clerical tasks, event and meeting logistics and coordination, HR process administration, answering HR-related questions for employees, running HRIS reports and record management, and assisting other...

Multiple Listings The SSU CRA is a site relationship management role to ensure sustainable trial start-up at Site. The Study Start-Up CRA is accountable for site selections as well as study-specific start-up activities and deliverables of assigned sites for Phase I-IV GDD trials within the country in adherence with monitoring procedures and processes in accordance with ICH/GCP, local regulations and SOPs. Proactive site preparation and early identification of real site needs and issues and close handover to execution CRA for all sites is key (from issue management to risk identification). This position can be based remotely anywhere in the U.S....

Clinical Study Monitor – Companion Diagnostics (CDx) The Clinical Study Monitor – Companion Diagnostics (CDx) is responsible for overseeing the day-to-day execution and monitoring of clinical studies involving in vitro diagnostic (IVD) devices, with a focus on companion diagnostics developed in collaboration with pharmaceutical and consortia partners. This role ensures that clinical performance studies are conducted in accordance with the protocol, applicable regulations (e.g., IVDR, GCP, FDA), and company SOPs. The Study Monitor will work closely with cross-functional teams including study team members, Quality and Clinical Affairs to support study site compliance and data quality. This position is ideal...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Purpose Through the application of scientific and medical training, clinical expertise,...

Our location Lake Forest, IL has an opening a Project Coordinator position. This person will be responsible to manage the development and implementation process of the company's products and services involving departmental or cross-functional teams focused on the delivery of new or existing products. What You’ll Work On Estimates project levels of effort and resource requirements by using standard estimating techniques and tools, and by working with appropriate staff to understand scope of effort. Prepares project plans, schedules and budgets by using project management tools such as Microsoft Project and by working with appropriate staff to understand tasks necessary to...

The Senior Clinical Trial Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. / Objective Serves as a primary source of medical accountability and oversight for multiple clinical trials Matrix management responsibilities across the internal and external network Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities Provides medical and scientific expertise to cross-functional BMS colleagues Position Responsibilities Medical Monitoring Contributes to and is a key member of a high performing Study...

OBJECTIVES/PURPOSE Provide Executive Coordinator support to Global Quality Compliance and Enterprise Systems and Global Audit and Supplier Quality Manages schedules (eg – periodic time analysis, appointment scheduling, schedule conflict management) Manages administrative deliverables (eg – travel arrangements, expense reporting, meeting agendas/presentations/materials/minutes, prepares reports, organization charts) Supports tracking and reporting on department projects Must be able to handle details of a highly confidential nature with discretion. Active participation in routine team meetings/projects and meeting minutes/distribution Engages across Global Quality (Above Site groups) Supports Global QUEST meetings – Scheduling/Calendaring and meeting support, as well as any other global Quality meeting as needed...

About This Role The Project Coordinator is responsible for coordinating function-specific operating activities for Strategy, Portfolio Operations, & Quality (SPOQ) Leadership Team, while providing direct operational support to the Head of R&D Quality & Compliance (RDQC). This role will be the primary point of contact for the Head of R&D Quality & Compliance and will be responsible for supporting daily activities of the RDQC LT. Core areas of activity will be cost center management (supporting budget tracking and planning), resource management (including staff planning for program support), collaboration on contracts (management and planning), project management support, and organizing leadership team...

The Enabling Facilities (EF) group within the Chemical Engineering Research & Development (CERD) Department is seeking a highly motivated individual to work in a fast-paced job that provides a high degree of practical technical, mechanical and planning responsibility. The Equipment Development and Facility Engineering (EDFE) Mechanical Coordinator position will report to the Associate Director, Engineering and will be a member of the MACS EF Team at the Rahway, NJ facility. EF is responsible for development of new technologies/capabilities, execution of capital and non-capital improvement projects, and the automation system assets spanning production, utility systems and associated infrastructure. EDFE's role within...

This position works out of our Alameda, CA location in the Abbott Diabetes Care Division, where we are focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology. The CRA II will assist in the clinical execution and management of all aspects of assigned clinical studies. This includes but not limited to planning and implementation of clinical studies from concept to clinical study report per timelines and quality standards. This is an on-site position, 5 days...

The Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical development and studies, including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director May Be Responsible For Evaluating pre-clinical and translational work for the purpose of generating early clinical development plans and Investigational New...

The Director (Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre-clinical to post-licensure). The Director will manage the entire cycle of clinical development for late-stage studies, including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. Specifically, The Director May Be Responsible For Planning clinical trials (design, operational plans, settings) based on these clinical development strategies Monitoring and managing the conduct of ongoing or new clinical...

POSITION SUMMARY The Clinical Trial Manager will be responsible for managing all aspects of clinical trials from start-up through close-out. The Clinical Trial Manager should have experience in managing all aspects of the trials independently, and is expected to provide functional expertise to ensure that study timelines, costs and quality metrics are met and the study is conducted in compliance with the study protocol, SOPs, and applicable regulatory requirements. PRIMARY RESPONSIBILITIES Manage the execution and conduct of all aspects of very complex clinical studies to ensure that timelines, cost, and quality metrics are met Responsible for selection of vendors/CROs and...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Organization Overview To provide stability program support to the Lilly Concord...

Associate Surveillance Coordinator Our location in Columbus, OH currently has an opportunity for an Associate Surveillance Coordinator . This role is responsible for coordination and execution of surveillance testing programs to assure the safety and compliance of Abbott Nutrition products and protect brand reputation by managing potential chemical hazards in food. You will work to implement testing strategies with regulatory and quality requirements across the global Abbott laboratory network. Accountability includes coordination of internal surveillance programs for ingredients and finished product with oversight from Project Manager. You will provide insight and awareness on potential data trends. WHAT YOU’LL DO...

The Publication Coordinator will work closely with Publication Managers, agency partners and internal and external publication stakeholders to assist with tracking, database entry, reports, updates, budgets and communication of Scientific Communications and Information Sciences (SCIS) projects and outputs. Responsibilities With minimal supervision Attend publication team meetings for planning knowledge and assist Publication Manager with note taking and meeting summary. Assist the Publication Manager in development and maintenance of publication plan slide decks. Assist with congress plan activities including development/maintenance of presentation trackers, document trafficking, author travel request management, archival of final versions and QR code process. Manage document flow...

The Director - Precision Medicine Initiatives is a senior sales role primarily responsible for establishing growth within an assigned geographic area through new account acquisition focusing on Pathology and the Hospital Laboratory Operation. The responsibilities include identifying, prospecting, and closing new business at potential accounts, mentoring the Account Managers and Molecular Oncology Specialists within the territory by acting as the Subject Matter Expert in the development of existing accounts, leading, coordinating and positioning the Account Managers and Molecular Oncology Specialists in the overall growth strategy for the territory and driving overall new growth in all accounts. The ideal candidate will...

Quality Systems Document Coordinator This position works out of our Tipp City, OH location in the Abbott Nutrition division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® – to help them get the nutrients they need to live their healthiest lives. Tipp City, Ohio, is one of Abbott’s newest nutrition manufacturing facilities with technology that enhances production efficiency and product quality. Join us...

Clinical Associate In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. What You’ll Work On Working under general direction, provides engineering, sales, educational and technical support in response to field inquiries from physicians, health care professionals, patients, and field sales staff, involving EP products. Performs work that involves a high degree of independence. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Exercises...