eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud – the foundation of digital trials. Together, the elluminate platform and digital data services give clients self-service access to all their data from one centralized location plus advanced analytics that help them make smarter, faster business decisions. OVERVIEW Senior Biostatisticians will work closely with clients and provide high level consulting services for statistical analysis, reporting, and statistical programming specific activities which may include development of statistics section of protocol, development of statistical analysis plan, randomization schedule, conducting statistical analyses, validating programming and reporting output, and developing statistical analysis report. Senior Biostatisticians will also work on statistical programming for development of analysis datasets, and clinical tables, listings, and graphs specific to trial reporting requirements. Senior Biostatisticians will work as needed assuring that all client work has met or exceeded client expectations. KEY TASKS & RESPONSIBILITIES - Provide consulting of statistics activities related to clinical trials. Fulfill the responsibilities of study statistician as required - Provide mentoring and QC of statistical programmer’s outputs; define analysis data specifications. If required, validate the statistical models used for programming - Act as study statistician - interact with client and with clinical team including programmers, clinical data managers, clinical protocol manager, and other relevant personnel. Ensure that programmers get correct specifications and data at appropriate time - Develop, review, and finalize the statistical analysis plan - Validate the programming deliverables and collaborate with applicable team members to rectify any issues related to statistical reporting and analysis - Develop randomization schedule, specifications, and guidelines - Wherever applicable, provide input in finalization of study specific data quality control plan and ensure appropriate data analysis and reporting - Wherever applicable, develop, validate and finalize the study specific list of table and table shells for clinical study reports and for study specific deliverables - Ensure that all comments from the clinical team with regards to statistical report delivered for study specific deliverables are being addressed appropriately - Analyze the data and contribute to trial progression related decisions by providing necessary input during trial specific deliverables including but not limited to blinded data reviews, and interim analyses - Collaborate with team members for regulatory reviews, representations, and supporting data analyses including the study or compound level exploratory analyses, ad-hoc analyses, and post- hoc analyses - Develop SAS programs to generate analysis datasets, and trial specific reporting including but not limited to tables, listings, graphs, queries, and patient profile reports - Ensure compliance with eClinical Solutions and industry quality standards, guidelines and procedures - Other duties as assigned CANDIDATE’S PROFILE Education & Experience - Master in Statistics, Biostatistics, or equivalent work experience preferred - Excellent knowledge of English - SAS® certification is preferred Professional Skills - 5+ years in Pharmaceutical/Biotechnology industry or equivalent statistical consulting and SAS programming role preferred - Strong experience with clinical study design development, analysis, and sample size determination - Experience with development of randomization schedule including development of IVRS specifications, and guidelines for appropriate usage of randomization schedule - Strong knowledge of ICH guidelines and other guidelines such as GCP, and 21 CFR Part 11 from different regulatory agencies including FDA, and EMEA - Experience in developing statistical analyses reports, and in conducting statistical analyses and reporting for various trial level deliverables including but not limited to blinded data reviews, interim analyses - Knowledge of coding dictionaries (WHO, COSTART, ICD-9, MedDRA) and clinical reporting processes - Knowledge of CDISC® related data models such as SDTM, and ADAM. Ability to develop ADAM model for analysis and reporting of clinical trial. Through understanding of SDTM data structures - Ability and experience of delegating tasks and leading projects. Experience of working on multiple clinical protocols at the same time - Ability to balance conflicting priorities - Excellent verbal and written communication skills - Detail oriented, ability to multitask with strong prioritization, planning and organization skills - Excellent team player Technical Skills - Experience of statistical procedures and latest developments and trends in statistical analysis methodologies. Knowledge of working in different therapeutic areas and related indications - Strong knowledge of statistical programming and ability to use various software systems like SAS, SPSS, and S-Plus. Ability to do statistical computing using R is a plus - Knowledge and ability to use various tools like J-Review, and Spotfire for effective data queries and analysis - Strong experience in various SAS software modules including SAS/STAT, and SAS/Graph - Thorough understanding of developing macros and SAS system - Thorough knowledge of design of experiments and statistical modeling. Experience of developing statistical designs for phase-I, phase-II, and phase-III clinical protocols - Experience of pooled data analysis and in designing specifications for integrating data from multiple trials - Knowledge of Analysis dataset model for development of analysis and programming specifications is a plus. Ability to develop ADAM models based on trial data - Thorough knowledge of analysis of various standard and non-standard safety domains. Knowledge of PK data modeling is a plus - Strong experience in efficacy reporting with regards to development of analysis sets, and treating missing values - Proficiency in Microsoft Office Applications Accelerate your skills and career within a fast-growing company while impacting the future of healthcare. We have shared our story, now we look forward to learning yours! eClinical is a winner of the 2025 Top Workplaces USA Award for Remote Work! We have also received numerous Top Workplaces Culture Excellence Awards celebrating our exceptional company vision, values, and work-life balance. See all the details here: https://topworkplaces.com/company/eclinical-solutions/ eClinical Solutions is a people first organization. Our inclusive culture values the contribution that diversity brings to our business. We celebrate individual experiences that connect us and that inspire innovation in our community. Our team seeks out opportunities to learn, grow and continuously improve. Bring your authentic self, you are welcome here! We are proud to be an equal opportunity employer that values diversity. Our management team is committed to the principle that employment decisions are based on qualifications, merit, culture fit and business need. Pay Range US Pay Ranges $150,000—$175,000 USD

• Support pre-award feasibility projects • Provide pre-award feasibility analysis and input for pre-award RFPs, including competitive analysis, historical recruitment analysis, standards of care, drug analysis, epidemiology analysis, site and country analysis. • Review clinical protocols, study assumptions, client information and study plans for US and global trials. • Present and explain feasibility analysis to BD/Clients, including the process, recommendations, and rationale. • Interface with colleagues, consultants and partners and collaborate with internal and external sources to gather and share feasibility information. • Undertake feasibility site outreach for pre award opportunities. • Participate and/or contribute to BDM and client calls. • Provide support to post-award feasibility projects • Undertake post-award, rescue, and standalone feasibility deliverables in alignment with study and client requirements. • Where appropriate, engage with patient advocacy groups and site networks to support study feasibility, recruitment, and successful delivery. • Support the analysis of the collected site data to provide accurate site identification, enrollment modeling and study strategy (ies)

Role Description New England Life Care currently has an opening for a Clinical Resource Nurse to be a lifeline, as-needed for our patients during the overnight hours. These nurses must reside in either New Hampshire, Maine, or Massachusetts. We would like these nurses to eventually be licensed in MA/NH/ME, although not an initial requirement. NELC will reimburse any costs associated with attaining additional licenses outside of the home license. The RN in this position is responsible for providing patient and VNA triage as well as subsequent coordination of care services. In addition, the RN in this position is competent in the duties of the Infusion Nurse as described by NELC, Inc. Responsibilities - Accepts patient phone calls and provides appropriate triage interventions, determines if a nursing visit is needed based on the unique situation of the patient. - If necessary, the resource nurse will coordinate a nursing visit (with NELC or Home Health Agency (HHA) nurse) in the appropriate time frame to meet the healthcare needs of the patient. - Accurately performs initial and ongoing patient assessments of home infusion/enteral therapy patients. - Provides comprehensive initial and ongoing patient and caregiver education relating to the prescribed home infusion/enteral therapy. - Effectively communicates with the scheduling team to facilitate adequate and timely PRN nursing visits. - Effectively communicates ongoing patient requirements, concerns, and/or changes in patient status / level of care to appropriate members of NELC multidisciplinary teams and on-call staff, as well as the HHA staff involved in meeting the patient’s home health needs. - Actively participates as a member of the patient’s care management team to identify and provide care coordination and/or guidance to care team, providers, and patients referred to NELC for infusion/enteral therapy, providing updated patient information as needed. - Comprehensively documents all interactions with patient and members of the healthcare team in the patient record and/or electronic progress notes. - Demonstrates competency in the use and troubleshooting of all equipment and/or supplies dispensed by NELC. - Demonstrates competency in home infusion medication administration, side effects, goals of therapy, and patient care expectations to include aseptic administration and monitoring of all therapy types provided by NELC. - Reviews needs and abilities of the patient and caregivers, participates in development and implementation of a patient specific training plan when appropriate as needed to assist Out-patient Resource team. - Assists in coordinating services with other home health agencies. - Acts as resource between NELC and all care providers. This includes, but is not limited to, the medical staff, care coordination team, and social services as needed. Qualifications - Associate degree or diploma in Nursing required. - BS in Nursing preferred. - Two (2) years intravenous therapy experience in hospital or homecare required. - Oncology experience preferred. - CRNI preferred. - R.N. license in good standing in the state(s) where providing care / services required. - Current BLS Certification required. Requirements - Valid driver’s license required. - Excellent driving record required. - Knowledge of HIPAA Privacy and Security Regulations preferred. - Knowledge of the Joint Commission accreditation process and overall JC standards preferred. - Excellent patient assessment skills required. - Working / practical knowledge of home infusion therapy administration / equipment use preferred. - Ability to communicate effectively with all customers and members of the healthcare team verbally and in writing. - Good interpersonal skills required. - Good organizational skills required. - Ability to work independently as well as a part of a team required. - Working / practical knowledge of microcomputer systems including patient documentation systems, Microsoft Office (Word, Excel, Outlook). - Dependability in attendance and job performance required. Benefits - Remote / Work From Home Position - Room for growth and potential for advancement - Generous employer-matched 403(b) savings program - Paid time off - And much more!

Benefits: - 401(k) - Bonus based on performance - Dental insurance - Flexible schedule - Health insurance - Opportunity for advancement - Vision insurance We are seeking a Per Diem Registered Nurse (RN) to support client intake, clinical compliance, caregiver competency oversight, and ongoing client management on an as-needed basis. This role provides flexible scheduling based on client volume and agency needs. This is not a bedside hospital position. Schedule & Structure • Per diem / as-needed basis • Flexible scheduling • Hours vary depending on client intake volume and regulatory needs • Ideal for RNs seeking supplemental income or schedule flexibility Key Responsibilities Client Intake & Assessments • Conduct initial and ongoing client assessments (in-home or virtual) • Evaluate client needs, risks, and service appropriateness • Develop, review, and update individualized care plans Compliance & Clinical Oversight • Ensure compliance with Minnesota home care regulations • Support documentation standards and audit readiness • Participate in surveys and quality improvement activities Caregiver Competency & Training • Conduct competency evaluations and skills assessments • Review and sign off on required documentation • Provide clinical guidance to caregivers and CNAs Clinical Support • Provide phone guidance for urgent care questions • Assist with changes in condition • Document and escalate issues appropriately Required Qualifications • Active Minnesota RN license • Minimum 3 years of nursing experience • Strong assessment and documentation skills • Ability to work independently • Reliable transportation for local travel Preferred Qualifications • Home care or hospice experience • Familiarity with Minnesota home care regulations • Experience supervising caregivers Optional Line You May Add (Very Important for Clarity) Compensation is structured per visit or hourly based on service provided. Flexible work from home options available.