Role Description As the Centralized Scheduler Licensed Practical Nurse (LPN), you provide clinical oversight to the Central Scheduling Team to ensure patients are scheduled appropriately and in alignment with organizational policies and procedures. You practice within the full scope of your licensure while supporting continuity, safety, and quality of care for patients and their families. You identify situations that require clinical judgment or decision making and appropriately escalate these concerns to leadership or the clinician. Through your guidance, you help foster a patient-centered scheduling process that promotes efficiency, accuracy, and overall well-being. Position Details: - Location: Remote (MA residents only) - Department: Hematology/Oncology/Infusion (Scheduling for Atrius Health) - Schedule: Full time, 40HRS Weekly M-F 8:30am-5pm If you are a Massachusetts-based resident, you will have the flexibility to work remotely as you take on some tough challenges. Qualifications - Graduate from a state-approved school of practical nursing - Current, unrestricted license to practice as a practical nurse in the Commonwealth of Massachusetts - American Heart Association Basic Life Support (BLS) Requirements - Infusion therapies (e.g., biologics, IV hydration, specialty medications) - Pre-infusion requirements such as labs, prior authorizations, and clinical screening - Experience in ambulatory care, specialty care, or infusion services is preferred - Ability to interpret clinical documentation to ensure appropriate scheduling and patient readiness - Maintains proficiencies in role-specific procedures as defined in organizational LPN competencies - Proficiency with electronic scheduling systems (Epic or similar platforms) - Ability to coordinate complex, multi-step appointments (infusion chair time, nursing coverage, pre-infusion labs) - Solid organizational skills with attention to accuracy and timing - Experience managing high volume scheduling workflows - Excellent verbal and written communication skills - Ability to collaborate effectively with healthcare team - Professional, patient-centered approach when interacting with patients and families - Communicates any pertinent information to the relevant members of the health care team verbally and/or through medical record. Maintains patient confidentiality - Under established protocols or under specific clinician direction, communicates with patients or family regarding specific test results or follow-up plans - Ability to identify scheduling conflicts, clinical concerns, or missing prerequisites - Sound judgment in escalating clinical questions to appropriate providers - Capacity to work independently while maintaining alignment with clinical protocols - Participates in organizational and departmental process improvement activities - Performs other duties as assigned Benefits - $5,000 Sign-on Bonus for External Candidates - Excellent compensation and benefits within 30 days - Generous PTO and paid holidays - Annual reviews and tuition reimbursement - Opportunities for continued career progression - Comprehensive benefits package, incentive and recognition programs, equity stock purchase, and 401k contribution (all benefits are subject to eligibility requirements) - Hourly pay for this role will range from $20.38 to $36.44 per hour based on full-time employment

• Increase proficiency in Trial Master File (TMF) set-up and maintenance (filing), both hard copy and electronic as assigned by project. • Increase proficiency in uploading and maintaining TMF files and folders in George Clinical’s file-sharing system by project as assigned. • Serve as second reviewer for TMF QC. • May function in the TMF Lead Role and assume responsibility for TMF setup, maintenance and oversight. • Assist with/complete end of study TMF filing (including site close out documents), QC and archival. • Further develop skills in preparing and participating in audit responses. • Perform QC of work (documents, emails etc.) prior to sending out to ensure quality product deliverables. • Further develop skills and knowledge of data entry and maintaining files/folders for Clinical Trial Management System by project as assigned. • Further develop skills and knowledge of assisting with data entry support, tracking and submission for investigator payments by project as assigned. • Works with CRA/CTM/PM during site start-up for feasibility, serving as point of contact for sites where applicable. • Assist with presenting final feasibility results to PM team and/or Sponsor. • Assists the sites in preparation, planning, organizing and collecting essential document packets (EDPs).

Role Description The Clinical Site Startup Specialist plays a pivotal role in the successful initiation of clinical trials by overseeing and coordinating all activities related to site startup. This position involves meticulous management, tracking, and facilitation of processes, from site selection through the Site Initiation Visit (SIV) phase. The specialist will be responsible for ensuring seamless execution of various tasks, including: - Regulatory document collection - Site contract and budget negotiations - IRB submissions and approvals - Equipment provisioning - Completion of a comprehensive greenlight checklist for drug release As the owner of the site’s contract and budget, the clinical site startup specialist will also be responsible for processing any amendments that are needed to site budget or contract. Qualifications - Bachelor's degree in a relevant field (life sciences, healthcare, etc.) - Previous experience in clinical trial site startup or a related field (2 years preferred) - Strong negotiation and communication skills - Experience managing clinical trial site contracts and budgets - Detail-oriented with excellent organizational and time-management abilities - Ability to work collaboratively in a team-oriented environment - Knowledge of regulatory requirements and guidelines governing clinical trials - Excellent written, verbal and interpersonal communication skills - Must be willing to travel up to 10% of the time Requirements - Collect, review, and track all required regulatory documents from selected trial sites - Ensure compliance with regulatory standards and guidelines - Engage in negotiations with clinical trial sites for contracts and budgets - Collaborate with the clinical trial manager and legal and finance teams to finalize agreements - Execute amendments to contracts/budgets as needed - Prepare and submit central Institutional Review Board (IRB) application in collaboration with the site and study team - Track local IRB submissions and approvals - Facilitate communication between Perspective, sites and IRBs to obtain timely approvals - Coordinate the provisioning of necessary equipment at trial sites - Ensure that all equipment is compliant with trial protocols and regulations - Execute a comprehensive checklist for drug release in collaboration with relevant stakeholders - Confirm that all site startup activities are completed and meet the required standards before drug release - Maintain open communication with internal and external stakeholders - Collaborate with cross-functional teams to address challenges and ensure a smooth startup process - Maintain accurate and up-to-date records of all site startup activities - Generate reports for management and project teams as needed - File all essential documents in the study eTMF Benefits - Equal employment opportunities to all employees and applicants for employment - Prohibits discrimination and harassment of any type - Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions

• Build pipeline through outbound (LinkedIn, sequencing tools, events) • Engage senior stakeholders (e.g., Clinical Ops, Patient Engagement, Procurement) • Qualify opportunities using structured frameworks (e.g., MEDDIC) • Run the full sales cycle: discovery → demo → proposal → negotiation → contract • Navigate complex enterprise buying processes • Manage timelines, stakeholders, and forecasting in CRM • Build strong relationships with enterprise clients • Identify expansion opportunities (pilots → multi-country rollouts) • Represent Curewiki at industry events (4–6/year) • Work with Growth, Product, and Leadership on strategy and key accounts • Share market feedback to shape product and positioning