Role Description This clinical field-based role requires strong clinical aptitude and the ability to operate effectively in a fast-paced, team-oriented environment. The Clinical Specialist builds trusted relationships with physicians and hospital staff while providing expert clinical support in the catheterization lab and operating room. Within the Vascular Therapies division, this role supports innovative technologies designed to diagnose and treat vascular conditions, including peripheral artery disease and pulmonary embolism. Our team continues to invest in a robust product portfolio and pipeline, expanding access to life-changing therapies across high-growth markets. We are seeking high-energy, driven professionals who are motivated to build a long-term, impactful career with Boston Scientific. Your responsibilities will include: - Assist in executing proactive regional plans that integrate clinical, sales, and service support to improve market share and enhance customer experience. - Serve as the primary clinical resource for case coverage, basic troubleshooting, specialty product usage, and customer training. - Attend procedures at customer accounts and advise physicians on clinical attributes and techniques associated with peripheral intervention products. - Represent the field organization during designated Boston Scientific clinical lab days. - Educate customers on proper clinical use and value of company products through presentations and demonstrations across multiple platforms. - Provide supplemental training support during product launches and for high-touch specialty products. - Respond to customer needs and product-related concerns by developing practical solutions or partnering with internal teams to deliver optimal outcomes. - Manage consignment inventory, including tracking, semiannual audits, expired product handling, and returns. - Ensure timely collection and reporting of required medical documentation related to procedural device use. - Support the Quality Policy by embedding quality into all aspects of work and maintaining compliance with all applicable quality requirements. Qualifications - Minimum of 3 years’ experience in a clinical, medical device, or related healthcare field or minimum of 6 years in related clinical field. - Bachelor’s degree or equivalent combination of clinical education (courses, certifications) and clinical experience. Requirements - Prior cardiovascular or endovascular clinical experience. - Minimum of 3 years’ experience in a competitive field-based clinical role, or a minimum of 6 years’ experience in a related clinical field. - Demonstrated ability to manage a large number of accounts and travel extensively within a territory. - Strong problem-solving skills and the ability to collaborate effectively while receiving coaching and direction from cross-functional partners. Benefits - The anticipated annualized base amount or range for this full time position will be $75,000 to $115,000, plus variable compensation governed by the Sales Incentive Compensation Plan. - Actual compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, and other relevant business or organizational needs.

Role Description We are seeking a qualified Biostatistician to provide statistical and clinical trial support for a Phase II clinical research effort supporting the Walter Reed Army Institute of Research (WRAIR). The selected candidate will support regulatory-focused statistical analysis activities, including CDISC-aligned deliverables and study closeout support associated with FDA submission requirements. This is a part-time consulting opportunity anticipated to run for approximately 10 months. Responsibilities - Perform statistical analyses in accordance with approved Statistical Analysis Plans (SAPs) - Support development, review, and validation of CDISC-compliant deliverables, including: - SDTM datasets - ADaM datasets - Define.xml documentation - SDRG/ADRG documentation - Generate and validate Tables, Listings, and Figures (TLFs) - Conduct data cleaning, quality control, and statistical validation activities - Support clinical study closeout and regulatory submission activities - Coordinate with clinical research and project teams to support data review and analysis workflows - Prepare technical documentation and contribute to study reports and presentations - Participate in project status meetings and provide progress updates Qualifications - Master’s degree or higher in Biostatistics, Epidemiology, Statistics, Public Health, or related field - Experience supporting clinical research or clinical trial studies - Experience developing or executing Statistical Analysis Plans (SAPs) - Experience with statistical programming and analysis using SAS, R, STATA, or similar tools - Experience generating statistical outputs including Tables, Listings, and Figures (TLFs) - Strong understanding of data validation, quality control, and analytical workflows - Ability to work independently and collaboratively in cross-functional scientific environments - Strong written and verbal communication skills - Able to successfully complete a background investigation and satisfy Government access requirements prior to beginning work Preferred Qualifications - Experience supporting FDA-regulated clinical trials - Hands-on experience with CDISC standards, including SDTM and ADaM - Experience preparing Define.xml, SDRG, and ADRG documentation - Experience supporting regulatory submission packages - Prior experience supporting Department of Defense (DoD), federal health, or military research organizations - Familiarity with clinical data structures, including demographics, adverse events, laboratory, and longitudinal outcomes data Work Location Primary support is associated with WRAIR in Silver Spring, MD. Remote work may be permitted, subject to task requirements and Government approval. Position Type Part-Time Consultant, Approximately 10-Month Period of Performance Pay and Benefits - Pay for this position is $50.00 hourly - Comprehensive benefits package, including: - Medical, dental, and vision insurance - 401(k) plan with company matching - Tax-deferred savings options - Supplementary benefits - Paid time off - Professional development opportunities

Role Description At EIM, we are reimagining healthcare education to humanize patient care in every community. We offer accessible lifelong learning to healthcare professionals transforming their communities. The Clinical Education Administrative Coordinator will play a pivotal role in the success of EIM's mission. Responsibilities - Assists Manager in creating agendas, scheduling meetings, taking relevant notes, and sending follow-up reminders to both EIM and UP teams. - Confirmation of clinical education sites and specialty settings after procurement of contracts across all healthcare education disciplines in a timely manner. - Accurate and efficient data entry and management of all clinical sites and personnel in the Clinical Education Management Systems. - Creation and management of Clinical Education timelines and reminders. - Build and maintain positive relationships with teammates and external stakeholders using effective in-person and virtual, email, and phone communication. - Assists Manager/Director in identifying areas of improvement and project needs across clinical education team as it relates to data management. - Assists Director of Clinical Operations and Clinical Education Managers in identifying and correcting data entry errors using appropriate quality control measures set by Director/Managers. - Track pertinent data and create relevant reports for internal and external stakeholders. - Manage clinical education internal and external contact lists. - Collaboration with Director of Clinical Operations and Clinical Education Managers as needed. - Maintenance of clinical education playbooks. - Other duties as assigned. Qualifications - College Degree or 1-3 years of relevant experience. - Must be action and goal oriented. - Ability to communicate effectively and professionally. - Must be agile and have an ability to learn on the fly. - Ability to thrive in a diversified working environment and deal with ambiguity. - Must possess strong interpersonal savvy. - Ability to establish and maintain effective working relationships with clinical education team. - Must be extremely well organized and detail-oriented. - Must be able to work effectively under pressure. - Ability to operate a computer and basic office equipment and demonstrate ability to learn new computer programs and have high technical aptitude. - Ability to take meeting notes and action items in a fast-paced setting. - Proficiency with Microsoft Office, Google, and other productivity enhanced applications. - Demonstrates a helpful, positive, and collaborative attitude. - Must be flexible and capable of multi-tasking. - Must take initiative and be a self-starter. Company Description Confluent Health, LLC and its affiliates are equal opportunity employers committed to building a diverse and inclusive workforce. We do not discriminate based on race, color, religion, sex, sexual orientation, gender (including pregnancy, childbirth, or related medical conditions), gender identity or expression, national origin, marital status, age, disability, veteran status, or other applicable legally protected characteristics. If you need assistance or would like to request an accommodation due to a disability, please contact us at careers@goconfluent.com.

• Manage all clinical operational and quality aspects of allocated studies, of moderate to high complexity, in compliance with ICH GCP. • In accordance to project specific requirements, may assume Lead CTM responsibilities on regional level, Clinical Study Manager (CSM) responsibilities or take on additional responsibilities, e.g. process improvements, manage complex programs, have wider management or project coordination responsibilities. • Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan. • Contribute to the development of the Master Action Plan (MAP) for providing clinical related documents. • Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central). • May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required. • Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings. • Collaborate with the clinical team and other departments as needed to meet deliverables of the project. • Regularly communicate with the team and leads team meetings to ensure that timelines, resources, interactions, and quality are maintained. • Responsible for the implementation and training of standardized clinical monitoring processes within the study and according to corporate standard policies. • Responsible for the timely archiving of documents and study materials for the department. • Ensure achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical activity timelines and metrics, providing status updates to the project manager, regularly reviewing projects using tracking and management tools, implementing recovery actions, reviewing monitoring visit reports, and managing CRF collection and query resolution. • Continuously monitor clinical trials to assess performance and ensure contractual obligations are met. • May routinely conduct Accompanied Field Visits (AFVs) and be accountable for project financials. • Communicate with study sites regarding issues such as protocol, patient participation, case report form completion and other study-related issues. • May coordinate all start-up activities, and ensure that essential document quality meets the expectation of Regulatory Compliance Review. • Ensure timely regulatory submissions (if appropriate) are addressed. • Reviews and follows up on all questions raised by ethics committees. • Provide input into preparation of forecast estimates for clinical activities. • Responsible for clinical resource management, assignment, delegation of clinical responsibilities and identification of additional resource requirements.