Before reading the job post, we encourage you to watch this video about our company. It gives you an inside look at how we started, the team and culture that made us successful, and where we're going. It's easy to read a job post and apply, but people often wonder about the culture and whether they would fit in. If you want to call Harrow your home and genuinely want to be part of a family and something big, then we encourage you to click this link and get to know us. Who is Harrow? Harrow (Nasdaq: HROW) is a leading provider of ophthalmic disease management solutions in North America. Harrow is an incredible entrepreneurial company – where we celebrate the ability of every member of the Harrow Family to be the CEO of their job. Harrow’s values have driven interest over the past decade in attracting high-performing professionals in a variety of disciplines. Members of our Harrow Family often express their pride in being a part of our commitment to (1) innovation, (2) patient access to affordable medicines, and (3) our track record of having never turned down an ophthalmologist doing mission work around the world – providing free medicines in support of mission work aimed at giving or maintaining the gift of sight to those most in need. We encourage you to learn more about Harrow and its unique culture to see if you’re the right person to help contribute as we build a truly exceptional company, one we are all so proud of! Harrow’s ophthalmic pharmaceutical portfolio is one of the most comprehensive in the industry, including: - An expanding Retina Portfolio including IHEEZO®, TRIESENCE®, BYOOVIZTM, and OPUVIZTM - A broad Dry Eye Disease product line, led by VEVYE® and bolstered by well-known adjacent ocular surface disease products such as FLAREX® and FRESHKOTE® - A peri-operative Surgical product line, led by TRIESENCE®, and BYQLOVITM - A Rare and Specialty product line, which includes various high-need and utility products such as ILEVRO®, NATACYN®, and VERKAZIA® - A robust internal development pipeline with multiple late-stage candidates, including MELT-300, MELT-210, H-N08, and CR-01 Job Summary The Manager of Regulatory Affairs will develop and execute regulatory strategies across the product lifecycle, including early-stage development, IND submissions, clinical trial support, NDA filings, and post-approval CMC activities. This role will lead regulatory CMC strategy while also serving as a key regulatory partner to Clinical Development for IND preparation, clinical trial applications, FDA interactions, and lifecycle management. The position collaborates cross-functionally with R&D, Clinical, Medical Affairs, Legal, QA, Manufacturing, and Commercial teams to ensure successful product development, regulatory approval, and compliance with FDA and global regulatory requirements. Core Responsibilities - Lead preparation, review, and submission of IND applications (including original INDs, amendments, annual reports, and safety updates) - Develop a regulatory strategy to support clinical development plans, including Phase 1–3 trial progression - Provide regulatory guidance for clinical protocol development and ensure alignment with FDA expectations - Lead and support FDA interactions, including Pre-IND, End-of-Phase, and other Type B/C meetings - Partner with Clinical and Medical teams to assess regulatory risk and develop mitigation strategies - Ensure compliance with GCP and applicable clinical regulatory requirements - Works closely with the executive leadership team to lead the development of regulatory strategies and objectives that result in successful registration and commercialization of Harrow’s ophthalmic products - Oversees regulatory matters connected to INDs, NDAs, and OTC ophthalmic products - As a regulatory product lead, ensures alignment of CMC, nonclinical, and clinical components to support successful IND, NDA, and post-approval submissions - Independently define CMC content (data and documentation) requirements for regulatory submissions and review content for conformance with established requirements - Plan and execute activities in support of INDs, NDAs, supplements, amendments, annual reports, and other regulatory submissions - Review and assess change controls for regulatory impact and manage appropriate submission requirements - Review and assess promotional materials for adherence to FDA guidance and current thinking - Serve as a primary contact with the US FDA, fostering strong relationships and acting as an effective regulatory advocate for Harrow Health - Provide regulatory guidance across all functional areas - Develop robust regulatory structures, processes, and procedures based on expert understanding and industry insight - Monitor the US regulatory landscape for changes affecting ophthalmic products and communicate impact to stakeholders Qualifications & Requirements - BS/BA Degree in a Scientific Discipline, an advanced degree preferred. - 6+ years of pharmaceutical Regulatory Affairs experience, including: - Direct experience authoring or leading IND submissions - Regulatory support for clinical trial programs (Phase 1–3) - CMC regulatory strategy and lifecycle management experience - Demonstrated experience interacting with the FDA on clinical development programs - Strong working knowledge of IND content requirements (Modules 2–5), ICH guidelines, and GCP regulations - Experience preparing briefing documents and participating in FDA meetings (Pre-IND, Type B, etc.) - Experience with NDA preparation and/or post-approval regulatory activities preferred - Experience supporting early-phase drug development and first-in-human studies strongly preferred - Ability to provide strategic regulatory guidance across development stages - Strong problem-solving ability, attention to detail, flexibility, and teamwork orientation - Excellent written and oral communication skills - Active participation in Agency/Industry groups/forums preferred Position Type - Remote Travel - Up to 30%

Title: Dietitian Nutritionist Category Nutrition Location(s) Frankfort, MI 49635, United States Salary Range $64600 to $83600 Job ID 986940 Job Description: Role Overview Join a great team where our residents and patients are at the heart of everything we do! Sodexo is seeking a Registered Dietitian for a part time (32 hours/week) position at Paul Oliver Memorial Hospital, a critical access hospital and subacute facility located in beautiful Frankfort, Michigan. In this role, you'll have the opportunity to provide care across inpatient, subacute and outpatient settings and serve as part of the larger Munson Healthcare clinical team. - Start with 3 weeks’ vacation and 3 personal days! - Remote flexibility - Reimbursement for AND dues, state licensure fees and CDR renewal - Professional growth via Sodexo's Career Ladder - Money toward continuing education events - Up to $5000 tuition reimbursement annually What You'll Do - offer compassionate care to patients in the acute, subacute and long term care setting; - serve as a hands-on leader in the Food & Nutrition Department; - support ongoing Performance Improvement and Quality Management projects; - provide training and education to department staff and interdisciplinary healthcare professionals; - collaborate with the food service operations team regarding meal provision and menu management; and - ensure DOH/State/Federal and company standards are being upheld. What We Offer Compensation is fair and equitable, partially determined by a candidate's education level or years of relevant experience. Salary offers are based on a candidate's specific criteria, like experience, skills, education, and training. Sodexo offers a comprehensive benefits package that may include: - Medical, Dental, Vision Care and Wellness Programs - 401(k) Plan with Matching Contributions - Paid Time Off and Company Holidays - Career Growth Opportunities and Tuition Reimbursement More extensive information is provided to new employees upon hire. What You Bring - Registered Dietitian credential and a great clinical knowledge base; - excellent communication, leadership and customer service skills; - experience with regulatory accreditation and establishing and maintaining standards of care; and - a strong commitment to excellence in all aspects of patient care. Who We Are At Sodexo, our purpose is to create a better everyday for everyone and build a better life for all. We believe in improving the quality of life for those we serve and contributing to the economic, social, and environmental progress in the communities where we operate. Sodexo partners with clients to provide a truly memorable experience for both customers and employees alike. We do this by providing food service, catering, facilities management, and other integrated solutions worldwide. Our company values you for you; you will be treated fairly and with respect, and you can be yourself. You will have your ideas count and your opinions heard because we can be a stronger team when you’re happy at work. This is why we embrace diversity and inclusion as core values, fostering an environment where all employees are valued and respected. We are committed to providing equal employment opportunities to individuals regardless of race, color, religion, national origin, age, sex, gender identity, pregnancy, disability, sexual orientation, military status, protected veteran status, or any other characteristic protected by applicable federal, state, or local law. If you need assistance with the application process, please complete this form. Qualifications & Requirements Minimum Education Requirement: Master's degree with completion of required coursework and supervised practice as dictated by the Accreditation Council for Education in Nutrition and Dietetics (ACEND) For those eligible for the registration exam prior to 1/1/24: Bachelor's degree with completion of required coursework and supervised practice as dictated by the Accreditation Council for Education in Nutrition and Dietetics (ACEND) Credentials Requirement: Meets eligibility requirements for Registered Dietitian Nutritionist (RD/RDN) by the Commission on Dietetic Registration (CDR) and will become registered within 120 days of hire. In some states and/or facilities the RD/RDN credentials is required at the time of hire Certification/licensure as required by state(s) of practice. In some states and/or facilities state certification/licensure is required at the time of hire Minimum Functional Experience - 3 years experienced practitioner able to work with minimal supervision

Role Description Imagen Technologies is seeking General Teleradiologists for part-time 1099 opportunities built around flexible 4-hour reading blocks. Whether you prefer weekday or weekend shifts, you can select the blocks that fit your schedule while earning premium compensation for focused reading sessions. You’ll interpret studies from a personalized worklist aligned with your expertise, including X-ray, ultrasound, MRI, and CT - all from the comfort of your home. This opportunity is ideal for radiologists looking to earn premium income in short, flexible shifts. Many physicians join our practice to supplement their income, maintain clinical engagement while reducing full-time hours, or create more time for family, travel, or personal interests. The only annual requirement is 2,000 wRVUs - how and when you reach that goal is entirely up to you. Flexible 4-Hour Shifts - Choose the reading blocks that work best for your schedule. - Weekday or Weekend Options: - 7:00 AM – 11:00 AM - 11:00 AM – 3:00 PM - 3:00 PM – 7:00 PM - 7:00 PM – 11:00 PM - Short, focused shifts allow you to maximize earnings without committing to long workdays. Technology & AI Innovation - Imagen’s technology is designed to help radiologists work faster, more efficiently, and with greater diagnostic confidence. - 6 proprietary FDA-cleared AI tools designed to improve efficiency and diagnostic accuracy. - Fracture detection across most of the body and a comprehensive Chest-CAD suite. - AI-enhanced automation that reduces manual steps while maintaining quality. - Technology trained on millions of manually annotated images and validated through real-world studies. - We pair experienced physician leadership with built-in AI safeguards to enhance accuracy and reduce liability. Compensation - Premium pay for 4-hour reading blocks with no cap on earnings potential. - Pay-per-study or pay-per-wRVU - the more you read, the more you earn. - Higher rates for weekend shifts. Qualifications - Board Certified or Board Eligible (ABR or AOBR). - 1+ year of experience interpreting studies. - Fellowship training preferred but not required. Benefits - Flexible scheduling - work when it’s convenient for you. - Fully equipped workstation shipped directly to your home. - Malpractice insurance included. - AI-optimized reporting platform designed for speed and efficiency. - 24/7 physician and IT support. Company Description Imagen’s mission is to ensure every patient receives the right diagnosis at the right time. We are a technology-enabled diagnostic imaging company focused on improving quality, accessibility, and affordability in medical imaging. - Our FDA-cleared AI software is embedded directly into our PACS platform, helping radiologists work more efficiently while maintaining the highest diagnostic standards. - We are a 100+ physician-led practice leveraging advanced technology to modernize radiology - improving accuracy, efficiency, and physician experience. Learn more about how Imagen is expanding access to high-quality imaging care: https://imagen.ai/solutions/

Role Description Performs a variety of functions and technical procedures necessary for patient admission, assessment, diagnosis, treatment, follow-up, and outcome evaluation. Participates in performance improvement, research, and educational activities. - Takes initial patient histories and performs physical examinations. - Initiates, documents, and communicates the plan of care and follows up to ensure complete screening and preparation of patients. - Performs daily patient rounds. - Writes orders for medications, laboratory work, and diagnostic tests. - Interprets laboratory and test results. - Confers with attending physicians, residents, nursing staff, and/or other care providers to ensure optimum quality of patient care. - Upon discharge, notes discharge summaries, prescriptions, and any referrals on patient charts. - Informs patients of the necessary post-discharge care instructions. - Performs related duties as required. All responsibilities noted here are considered essential functions of the job under the Americans with Disabilities Act. Duties not mentioned here, but considered related are not essential functions. Qualifications - Bachelor’s Degree, required. - Graduate of an accredited (Accreditation Review Committee for Physician Assistant Programs ARC-PA) program, required. - Current license to practice as a Physician Assistant (PA) by the New York State Department of Education, required. - Current NCCPA Certification from the National Commission on the Certification of Physician Assistants (NCCPA), required. - Current BLS certification, required. Company Description