• The Clinical Research Program Specialist plays a key role in the lifecycle of SI-BONE’s clinical studies. • Works with the team to plan, design, and implement clinical research projects. • Collaborates cross-functionally to gather input from other key departments including regulatory affairs, medical affairs, marketing, and R&D. • Manages clinical study sites and coordinates activities to ensure overall compliance with the protocol and clinical objectives. • Conducts clinical site monitoring, both remote and onsite. • Maintains a high level of professional expertise through reading literature, attending society meetings, and interfacing with physician customers. • Collaborates with study team to draft materials including case report forms, site presentations, and other documents as applicable. • Responsible for performing all duties in compliance with all applicable worldwide regulatory requirements as included in the scope of the SI-BONE Quality Manual.

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 As the Clinical Nurse Coordinator (LPN), you'll support care navigation across the continuum of cancer by facilitating guideline-aligned treatment, symptom tracking, and member re-education. You'll collaborate with RNs, providers, and interdisciplinary teams to ensure care plans, referrals, and authorizations are coordinated and care transitions are smooth. As the LPN of a growing department, you'll also assist with clinical trial participation, manufacturer assistance programs, and identify grants or foundations to provide insight and guidance to the team and our members. You'll review active infusion medications to coordinate with external resources for infusion services, help with claim reviews, and manage administrative tasks, all while maintaining your own caseload of members and following up per each member's unique cadence. You'll be an integral expansion of other team members' responsibilities by emphasizing coordination, documentation, member engagement, and resource navigation within an LPN scope of practice. How You'll Contribute - Maintain regular contact with assigned oncology members via phone, text, email, and video calls to provide follow-up and support. - Assist and coordinate with the RN in member care delivery by communicating with providers and pharmacies and facilitating referrals to third-party infusion services for cost containment. - Identify, coordinate, and facilitate referrals to infusion services, clinical resources, or supportive care programs. - Address social determinants of health (SDOH) affecting members' access to care, adherence, and overall well-being. - Provide education and guidance on treatment logistics, medication access, and community or program resources, reinforcing physician-directed care. - Provide emotional support and connect members to counseling, support groups, survivorship resources, and other supportive services. - Collect, document, request, and send member information in the EHR per HIPAA; escalate clinical concerns to the RN as appropriate. - Track member interactions and support the RN in meeting enrollment, engagement, and quality metrics. - Collaborate with the RN and interdisciplinary team to ensure members receive timely, coordinated oncology care. Qualifications - LPN/LVN license in good standing within a compact state, plus willingness to obtain licensure in other states as needed. - A minimum of 4 years' LPN/LVN experience, plus clinical experience in oncology and infusions are required. - Experience with care navigation, treatment support, and/or complex case management is strongly preferred. - Must live in either PST, MST, or CST and flex your work schedule to support members in every US time zone, which means working some evening and weekend hours. - Ability to speak, write, and communicate fluently in Spanish is strongly preferred. - Utilization Review and/or Care Management preferred. - Experience working 100% remote as a nurse is highly preferred. - Ability and willingness to travel occasionally, which will include overnight stays for corporate gatherings, conferences, and health fairs. - Ability to attend and professionally engage in video meetings. - Proficient technological skills, meaning you can effectively and efficiently use computers, peripheral equipment, and applications/systems, including Microsoft products. - Autonomous self-starter who is comfortable with ambiguity. - Creative mindset and ability to appropriately challenge the status quo. - Superb written and oral communication skills. - Ability to overcome obstacles with a ‘yes if...' approach. - Ability to effectively balance competing deadlines without losing focus on the bigger picture. - Reliable internet and power with a designated area to conduct work with minimal interruptions. Benefits - Market competitive salary, plus potential annual merit increases and bonuses contingent on the company's fiscal performance. - Generous time off and paid holidays because we value recharging. - Exceptional healthcare coverage, with the majority of medical, dental and vision premiums covered by us. - 401k with generous employer match.