• Review, understand, and assess clinical data before it is reviewed by Medical/Client. • Communicate and present the relevant trends and findings of the clinical review to the Study Team and the Client. • Ensure that the clinical database and regulatory projects maintain the highest level of integrity. • Collaborate with Client, subcontractors, and Study Team members to meet project timelines and Client expectations for clinical data review. • Review CRFs, data quality review plans, and other clinical study reports as needed. • Propose methods to improve collaboration, efficiency, and excellence in data-related review deliverables to the Chief Scientific/Medical Officer, Clinical Operations and Biometry. • Partner with Study Team in the development of data review plans for individual clinical studies. • Provide continuous review and interpret relevant clinical data, applying clinical expertise to derive meaningful insights. • Analyze and track potential safety events within a given trial and across trials for assigned programs. • Contribute to discussions with Study Team and/or Client regarding modifications in the study and/or strategy based on clinical review.

Why Orthofix? Guided by our organizational values – Take Ownership | Innovate Boldly | Win Together – we collaborate closely with world-class surgeons and other partners to improve people’s quality of life. At Orthofix, we want team members who build relationships and share knowledge, challenge the status quo, and deliver results every day to help us achieve our vision to be the unrivaled partner in Med Tech. Our global team of over 1,600 employees brings to market highly innovative, cost-effective, and user-friendly medical technologies that heal musculoskeletal pathologies for patients and the healthcare professionals who treat them. Looking to change people’s lives? Look no further. JOB PURPOSE The Clinical Specialist II provides clinical, technical and product knowledge support to existing and potential customers. Builds and maintains solid customer relationships and provides pertinent and precise training at all levels. You are a product expert and will advise surgeons and staff during surgery, on all aspects of the systems technology. ESSENTIAL FUNCTIONS AND RESPONSIBILITIES The following are the essential functions of this position. This position may be responsible for performing additional duties as tasks as needed and assigned. - Manage designated accounts within specified territory by providing on-site consulting, guidance and assistance to physicians and Operating Room (OR) personnel to ensure product and tools accuracy in usage. - Educate/train physicians and relevant hospital personnel on the use of the company’s navigation technologies, associated equipment and instruments at installations, trade shows and labs to insure procedural efficiency. - Develop effective training resources for hospital staff to facilitate training of associated staff on product. - Work with key surgeons to obtain product feedback to communicate to product development teams for continuous technical enhancement. - Analyze, resolve, and repair issues through detailed analysis and in-depth understanding of the product. - Provide prompt customer support by use of comprehensive case collecting process, ensuring client satisfaction. - Provide independent support for all Cranial and Spine related cases with accurate knowledge and answer relevant queries in a timely manner. - Confidently lead evaluations, labs, demos, and installations to demonstrate value in product and associated tools. - Successfully and effectively train new Clinical staff on processes and procedures and other associated job-related responsibilities. - Keep abreast of developments regarding 7D (SeaSpine) and competitive Image Guided Surgery products and services through ongoing training and individual research and development. - Support sales efforts by coordinating closely with the Area Sales Manager to leverage your clinical expertise in developing sales opportunities. - Partner with other cross functional teams in selling the clinical benefits of the company’s products, drive continuous account growth and case volume. MINIMUM QUALIFICATIONS The requirements listed below are representative of the education, knowledge, skill and/or ability required for this position. Education/Certifications: - Bachelor’s Degree (B.A.) in Nursing and other relevant fields Experience, Skills, Knowledge and/or Abilities: - Two (2) to five (5) years of experience in medical device/navigation; or related experience. - Experience in MRI & CT, intra-operative imaging, stereotactic navigation, optics, or robotics. - Hands on experience in a hospital or OR setting. - Experience in informatics – PACS, DICOM, networking. - Strong interpersonal and communication skills - Strong communication of technical subjects to a wide range of audiences - Quick analytical thinking and problem-solving skills - Independent worker, strong work ethic, and self-motivated - Strong computer literacy - Ability and willingness to travel throughout the United States - Off-hours, weekend, and holiday support at times - Flexible day-to-day availability and schedule PREFERRED QUALIFICATIONS The education, knowledge, skills and/or abilities listed below are preferred qualifications in addition to the minimum qualifications stated above. Education/Certifications: - B.S. in Biomedical or Clinical based field. Additional Experience, Skills, Knowledge and/or Abilities: - Knowledge of video integration and routing - Competency in leading evaluations - Proficient with ETQ documentation - Ability to successfully train new Clinical Specialist hires - Prior experience in sales or customer services is an asset - Proficient in the use of PC software applications, including Microsoft Office. PHYSICAL REQUIREMENTS / ADVERSE WORKING CONDITIONS The physical requirements listed in this section include, but are not limited, to the motor/physical abilities, skills, and/or demands required of the position in order to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to allow qualified individuals with a disability to perform the essential functions and responsibilities of the position. - The position requires frequent or continuous standing, walking, bending, stooping, kneeling, or crouching and pushing and/or pulling. - There is frequent heavy lifting of 40lbs or more. - Continuous and frequent travel is also required. DISCLAIMER The duties listed above are intended only as representation of the essential functions of this position. The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or a logical assignment to the position. The job description does not constitute an employment agreement between the employer and employee and is subject to change at the sole discretion of the employer. Nothing in this document alters an employee’s at-will employment status. We are committed to providing equal employment opportunities to all employees and applicants without regard to race (including traits historically associated with race, such as hair texture and protective hairstyles, including braids, locks, and twists), ethnicity, religion, religious creed (including religious dress and grooming practices), color, caste, sex (including childbirth, breast feeding, and related medical conditions), gender, gender identity or expression, sexual orientation, national origin, ancestry, citizenship status, uniform service member and veteran status, marital status, pregnancy, age (40 and over), protected medical condition (including cancer and genetic conditions), genetic information, disability (mental and physical), reproductive health decision-making, medical leave or other types of protected leave (requesting or approved for leave under the Family and Medical Leave Act or the California Family Rights Act), domestic violence victim status, political affiliation, or any other protected status in accordance with all applicable federal, state, and local laws. This policy extends to all aspects of our employment practices including, but not limited to, recruiting, hiring, discipline, termination, promotions, transfers, compensation, benefits, training, leaves of absence, and other terms and conditions of employment.

We understand that the world we want tomorrow starts with how we do business today, and that’s why we’re inspired to make A Better World for Pets. Antech is comprised of a diverse team of individuals who are committed to each other’s growth and development. Our culture is centered on our guiding philosophy, The Five Principles: Quality, Responsibility, Mutuality, Efficiency and Freedom. Today Antech is driving the future of pet health as part of Mars Science & Diagnostics, a family-owned company focused on veterinary care. Current Associates will need to apply through the internal career site. Please log into Workday and click on Menu or View All Apps, select the Jobs Hub app, then click the magnifying glass to Browse Jobs. PURPOSE OF JOB: The Clinical Pathologist will diagnose disease and cause of death in companion and laboratory animals by examining body tissues, fluids, and hematologic specimens. The Target pay range for this position is $130,000 - $160,000 annually. At Antech, pay decisions are determined using factors such as relevant job-related skills, experience, education, training, and budget. ESSENTIAL DUTIES AND RESPONSIBILITIES: To perform this job successfully, an individual must be able to satisfactorily perform each essential function. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. - Describe and interpret cytologic preparations from fine needle aspirates, body fluids and hematologic specimens to determine the cause of disease or death in animals - Prepare pathology narrative reports of cytologic, hermatologic and clinical pathology data. - Dictating medical evaluations using Dragon and other dictating software - Consult with Veterinarians about diseases detected in sample tissues and fluids based on test results and clinical findings through Skype, phone and email - Participate in Pathology rounds bi-weekly - Describe, interpret and generate reports for research samples in companion and laboratory animals, including cerebrospinal fluid, bone marrow aspirates and hematologic data. - Provide medical second opinions as requested by clients or from colleagues. - Describe and interpret histopathologic findings from bone marrow core biopsies. - Provide scientific and technical advice to laboratory staff and Veterinarians with regard to sample collection and submission. - Stay current on veterinary and medical practiced through continuously reviewing journal publications, text books and attending continuing education conferences and seminars - Participate in the Quality Control program - Maintain proficiency in clinical diagnostic skills - Assist in other duties relevant to Clinical Pathology and other lab services - May be asked to participate in enterprise initiatives special projects or other duties as assigned. EDUCATION/EXPERIENCE: - Doctor of Veterinary Medicine (DVM/VMD) degree or equivalent - Diplomat of American College of Veterinary Pathologists - Must be licensed to practice veterinary medicine in respective state REQUIRED SKILLS AND ABILITIES: - Excellent written and verbal communication skills. - The ability to think outside the box, with a keen attention to detail. - Analytical and problem solving skills - Ability to prioritize - Strong passion for helping people and animals - Organized with the ability to multi-task in a fast paced environment - Previous experience in a lab environment a plus - Proven ability to work effectively with clients and management is required - The ability to work effectively remotely with minimal supervision - Previous experience with Dragon software a plus. - Previous experience with Dicom viewers a plus - Fluency in English About Antech Antech is a leader in veterinary diagnostics, driven by our passion for innovation that delivers better animal health outcomes. Our products and services span 90+ reference laboratories around the globe; in-house diagnostic laboratory instruments and consumables, including rapid assay diagnostic products and digital cytology services; local and cloud-based data services; practice information management software and related software and support; veterinary imaging and technology; veterinary professional education and training; and board-certified specialist support services. Benefits Antech offers an industry competitive benefits package and continues to invest in and evolve benefits programs that meet the health, wellness and financial needs of our associates. Benefits eligiblity is based on employment status. - Paid Time Off & Holidays - Medical, Dental, Vision (Multiple Plans Available) - Basic Life (Company Paid) & Supplemental Life - Short and Long Term Disability (Company Paid) - Flexible Spending Accounts/Health Savings Accounts - Paid Parental Leave - 401(k) with company match - Tuition/Continuing Education Reimbursement - Life Assistance Program - Pet Care Discounts Commitment to Equal Employer Opportunities We are proud to be an Equal Opportunity Employer - Veterans / Disabled. For a complete EEO statement, please see our Career page at Antech Careers. Note to Search Firms/Agencies Antech Diagnostics, Inc. and its subsidiaries and affiliates (Antech) do not compensate search firms for unsolicited assistance unless they have a written search agreement with Antech and the requisition is position-specific. Any resumes, curriculum vitae, and other unsolicited assistance from search firms that do not have a written search agreement or position-specific requisition submitted to any Associate of Antech will be deemed the sole property of Antech and no fee will be paid in the event the candidate is hired by Antech.

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