Benefits: - 401(k) - Competitive salary - Dental insurance - Health insurance - Paid time off - Stock options plan No visa sponsorship is available. Home base location – Midwestern USA. Able to work remotely and travel frequently (approximately 50% to 60%). For those history buffs i-Lumen Scientific™ is an Ophthalmology Bioelectric Stimulation company, whose focused on developing a medical device therapy for patients with vision loss due to intermediate to advanced dry age-related macular degeneration (dAMD). We know, that’s a mouth full! Who doesn’t want to keep their eyesight? Close your eyes for a moment or look through a pair of glasses with a dark smudge in the middle. A smudge so dark you can’t see through it. Now imagine a day when circumstances change and that’s you. Following that your doctor told you, “that’s just the way it is, and it will only get worse!” Macular degeneration is the leading cause of vision loss for older adults, has no cure, and there are limited treatments options. Our goal is to change that. Our Mission i-Lumen™ is working to change the status-quo by pioneering a new medical device field in ophthalmology intended to improve vision for AMD patients. This new therapy has the potential to address a large unmet patient population in the practice of ophthalmology. The i-LUMEN™ system and therapy, developed by i-Lumen Scientific, utilizes a revolutionary, non-invasive, medical device, to deliver proprietary pulsed microcurrent stimulation for the treatment of intermediate to advanced dry AMD. You guessed it, with i-Lumen™ technology, there may finally be hope for those with vision loss due to dry AMD. Are you interested in joining us on this journey? If so, we’d like to tell you a bit more about ourselves. Our Peeps Our team includes problem-solvers, car enthusiasts, runners, animal lovers, concert goers, and world travelers who are dedicated to improving vision for those impacted by AMD. The cool thing is, some of us have worked together in the past and we actually like each other. We are passionate about finding great people to join our team. If you are eager to invest your time, talent, and energy in our goal of making the world better one eye at a time, we encourage you to read on! It’s not just a job If you been in start-ups you know hat-wearing and communication are keys to success. As we hire, expand and execute a global clinic trial, we need a cohesive team of high performers, who take accountability, know what good looks like and can bring their “A” game each and every day. We don’t do group think, but rather welcome ideas and opinions to ensure the best path forward. Have an idea? Bring it! Have a better more efficient way to get from A to Z? Suggest it! Do you ensure safety and quality of work are uncompromising? Then i-Lumen may be the place for you! Building for a better tomorrow. i-Lumen is seeking a Senior Clinical Research Associate (Sr. CRA) located in the Midwest to participate in activities to support the execution of clinical studies to ensure compliance with applicable regulations, Good Clinical Practice (GCP) Guidelines, and i-Lumen Scientific’s Standard Operation Procedures (SOPs). As a start-up, we are a small team but growing. This means a fast-paced, think on your feet, being accountable and someone others can rely on kind of environment. We don’t’ have every bell and whistle in our quiver and we create things as we go, ensuring safety and quality in all we do. We do not compromise excellence and depend on each other to do what we say we will do. Still interested? Let’s get into the details. Responsibilities: · Work under minimal guidance and participate in the conduct of clinical research projects and protocols, contributing technical and clinical expertise. · Contribute to the execution of clinical trials in terms of all operational aspects of study start-up through close-out including supplying study materials to sites. · Participate in the preparation of clinical study specific training materials, as needed. · Support the administration of clinical studies according to good clinical practices (GCP) and standard operating procedures (SOPs), which may include management of communications with contract vendors, CROs, clinical study team, and clinical sites. · Review study documentation for accuracy and completeness in accordance with protocol, GCP, and regulatory requirements. · Maintain study documentation within the Sponsor Trial Master File (TMF) and other study management systems, tracking, and reporting trends to the clinical team. · Clinical monitoring activities may include the following: · Participate in the evaluation and selection of Investigators and study sites, including site qualification and site initiation visits. · Perform site monitoring visits including close-out (on-site and remote) in accordance with the Clinical Monitoring Plan (CMP) to ensure compliance with the Protocol, applicable regulations, EC, GCP, and i-Lumen SOPs, guidelines, and policies. · Communicate visit findings with site personnel, including a follow-up letter for distribution to the Principal Investigator (PI) and appropriate site personnel. · Prepare site visit reports and correspondence for all visits conducted in accordance with the CMP. · Identify site needs and provide solutions to facilitate the clinical study process. · Act as primary point of contact for study sites as requested. · Assist in initial and ongoing site personnel training, as required, including case support and training of clinicians in use of study device(s). · Identification and escalation of protocol deviations, discrepancies in data, and non-compliance to study protocols, applicable regulations, GCP, and SOPs. · Collaborate with study team personnel and i-Lumen Clinical Team to secure Investigator compliance and provide solutions if needed. · Participate in development and ongoing review of CMP and monitoring tools and resources. · Support in recruitment activities which may include the following: · Collaborate with the Clinical and Recruitment Team on the development of patient recruitment materials. · Engage with sites on the internal recruitment procedures and identification of study participants. · Ability to travel approximately 50%-60% · Other duties as assigned. Do you have the following qualifications? · Seven (7)+ years clinical research study monitoring for medical device or related experience. · Experience in an Ophthalmology indication is highly preferred. · BS degree or equivalent experience. · Knowledge of federal and local regulations and policies pertinent to research involving human subjects. · Knowledge of ICH GCP and Declaration of Helsinki. · Excellent communication, interpersonal and organizational skills. · Ability to collaborate in a team environment as well as work independently. · Self-starter with the ability to manage multiple projects in a dynamic environment. Think you have what it takes? If we piqued your interest, we hope you will pique ours and follow the prompts to apply! This is a remote position.

• Develop, test, execute, and maintain SAS and R programs for statistical analyses, including central tendency analysis, categorical analysis, and concentration‑QTc analysis • Validate statistical results through double programming and independent verification • Prepare tables, figures, and listings (TFLs) in accordance with approved statistical analysis plans • Review final outputs and reports to ensure alignment with planned statistical methodologies • Perform quality checks on CDISC‑formatted analysis datasets (ADaM) • Support research programs by providing statistical results and insights to senior team members and department management • Interpret and communicate statistical methodologies, results, and conclusions to Principal/Senior Principal Biostatisticians, Medical Writing, and Scientific Teams • Train team members on standard operating procedures and standard statistical methodologies • Drive process improvements to enhance operational efficiency and data quality • Manage timelines, client commitments, and on‑time delivery for assigned projects • Maintain accurate deliverable tracking, status updates, and milestone dates in team tracking tools • Assist with the development, coordination, maintenance, and enforcement of quality standards, including SOPs, SWIs, playbooks, checklists, and templates.

About TimeDoc Health Founded in 2015, TimeDoc Health provides Virtual Care Management services that help patients with chronic conditions stay connected to their care between office visits. Through technology and compassionate outreach, we support better health outcomes and help patients stay out of the hospital. Our work makes a real impact on thousands of patients nationwide. The Role We are hiring Care Coordinators to support patients with chronic conditions through Chronic Care Management (CCM). This is a phone-based, productivity-driven role where you will spend most of your workday on the phone speaking with patients, coordinating care, and documenting interactions. This role is ideal for clinical professionals who are comfortable with high call volume, structured schedules, and meeting daily productivity metrics in a remote environment. Work Schedule & Expectations - Full-time, 40 hours per week - Coverage required Monday–Saturday, 8:00 AM–6:00 PM in the time zone you support. - Fixed schedule assigned (no alternate shifts available) - Expect to spend 7–8 hours per day on the phone - Productivity and quality metrics are required and monitored What You'll Do - Conduct monthly CCM phone calls with assigned patients - Make 30–50 outbound calls per day - Complete required patient interactions to meet CCM service goals - Educate patients on chronic conditions and care plans - Coordinate care with provider offices, pharmacies, and community resources - Identify gaps in care and social determinants of health - Create and update personalized care plans in the EMR - Accurately document all patient interactions - Maintain HIPAA compliance and patient confidentiality Requirements - Minimum 1-3 year of experience as a CMA/RMA, LPN, or RN - Active certification or multistate license for LPN/RN - Strong verbal and written communication skills in English - Comfortable being on the phone most of the day - Experience with EMR/EHR systems - Organized, reliable, and able to work independently in a remote setting Preferred: - Geriatric patient experience - Care coordination or case management experience - Strong verbal and written communication skills in Spanish Work Environment & Equipment - Private, quiet home office with no interruptions - Reliable high-speed internet (100 Mbps or higher) - Second monitor required - Company laptop and required software provided Benefits & Perks - Medical, dental, and vision insurance - Paid time off and paid holidays - Fully remote work environment - Supportive team culture with opportunities for growth - Career advancement as TimeDoc Health continues to expand - Meaningful work focused on keeping patients healthy and out of the hospital TimeDoc Health is an Equal Opportunity Employer. TimeDoc Health does not discriminate on the basis of race, religion, color, sex, gender identity or expression, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment decisions are made on the basis of qualifications, merit, and business need.

We are currently looking for a Clinical Nurse Trainer for a 100% remote position on a large federal government project supporting the Department of Veterans Affairs (VA) healthcare system. This role is responsible for designing, delivering, and evaluating training programs focused on mental health topics, including suicide prevention and safety planning interventions. The selected candidate will bring strong clinical expertise, experience supporting the veteran population, and familiarity with telehealth-based service delivery models. The candidate must reside within the continental US. Responsibilities: - Design and develop comprehensive training materials and modules focused on mental health assessment, suicide prevention, and safety planning interventions tailored for VA clinicians and staff. - Facilitate engaging and effective classroom and virtual training sessions, including telehealth-based delivery formats, for multidisciplinary VA staff. - Serve as a subject matter expert on evidence-based mental health practices, suicide risk mitigation, and telehealth service delivery. - Evaluate training effectiveness through participant feedback, performance metrics, and quality improvement initiatives. - Collaborate with VA leadership, education coordinators, and stakeholders to align training programs with national standards and VA priorities. - Incorporate adult learning principles and instructional design best practices into all training initiatives. - Promote trauma-informed, veteran-centered care principles across training content and delivery. - Contribute to team objectives and take on additional responsibilities as needed. Requirements: - Bachelor’s degree in Nursing; Master’s degree preferred. - Active Registered Nurse (RN) license in good standing. - 3–5 years of experience in mental health and suicide prevention, preferably within the VA healthcare system. - Direct experience with safety planning interventions and suicide risk assessment protocols. - Demonstrated experience developing and facilitating both in-person and telehealth training programs. - Strong communication, presentation, and group facilitation skills. - Experience applying adult learning principles and instructional design methodologies. - Commitment to trauma-informed, veteran-centered care practices. Additional Qualifications: - Prior experience supporting VA clinical education or national VA training initiatives. - Familiarity with telehealth platforms and remote training technologies. - Experience collaborating with interdisciplinary healthcare teams. - Knowledge of VA policies, procedures, and suicide prevention initiatives. Benefits: - Medical/Dental/Vision. - 401k with Employer Match. - PTO + Federal Holidays. - Corporate Laptop. - Training Opportunities. - Remote Opportunity. Note: Selected candidates will be required to complete fingerprinting at a government facility and undergo a background check as part of the hiring process. Equal Opportunity Disclaimer: VetsEZ is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability, or protected veteran status. Sorry, we are unable to offer sponsorship at this time.