This page tracks remote case coordinator openings that are location-eligible for Ohio.
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$17 - $60,000
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Role Description The ECM Nutritionist delivers member-centered nutrition support that reduces risk, improves outcomes, and removes barriers to accessing evidence-based lifestyle support. This role partners closely with case management, utilization management, pharmacy, behavioral health, and other internal partners to advance chronic disease prevention and management (e.g., diabetes, hypertension, obesity) through nutrition education, health literacy, benefits navigation, and digital care tools. The ideal candidate is an empathetic advocate who blends nutrition science with practical, culturally competent care strategies. Essential Functions - Provide nutrition education via phone and digital platforms for members with diabetes, prediabetes, hypertension, obesity, CKD, and CVD risk to enhance understanding of the relationship between diet, chronic conditions, and overall wellness. - Develop culturally appropriate meal plans and dietary recommendations tailored to members’ health conditions, preferences, and socioeconomic factors. - Collaborate with case managers, pharmacists, behavioral health clinicians, and other partners to align goals, reconcile care plans, and optimize medication/lifestyle synergy. - Refer members to available tools and resources to support lifestyle management. - Maintain accurate and timely documentation, including care goals, interventions, progress, follow-up, and referrals. - Other duties as assigned. Qualifications - Bachelor’s degree in health education, health promotion, food science, nutrition, or a related health program required. - Lifestyle Management and/or Wellness Coaching certifications strongly preferred. Requirements - 3-5 years’ experience working with individuals with chronic conditions and lifestyle-related comorbidities. - Demonstrated ability to create culturally sensitive nutrition plans and communicate effectively with diverse populations. Position Competencies - Accountability - Analytical Thinking - Collaboration - Communication - Customer Focus - Functional Expertise - Initiative Physical Demands This is a standard desk role requiring extended periods of sitting and computer work. Work Environment Remote Benefits - Medical, Dental, Vision, Life and Disability Insurance - Generous Paid Time Off - Tuition Reimbursement - EAP - Technology Stipend
At Arriello, we provide Pharmacovigilance, Quality & Compliance, and Regulatory Affairs services to global pharmaceutical and life sciences companies, helping them meet regulatory requirements and protect patient safety. We are a growing business with a collaborative culture focused on high‑quality delivery, continuous improvement, and giving people the space to do their best work. Our values guide how we work: Inclusive – We value fairness, respect, and learning from one another. Dedicated – We deliver practical, client‑focused solutions. Innovative – We work together to find better ways forward. Passionate – We build strong relationships and care about the quality of what we do.
Role Description This is a remote position. As a Global Drug Safety Associate , you will support the delivery of high‑quality clinical and post‑marketing safety activities. You will work closely with senior Drug Safety colleagues to process safety cases, maintain documentation, and support compliance and operational tasks across multiple projects. Key Responsibilities - Support the processing of safety cases from clinical trial and post‑marketing sources, including AEs, SAEs, and SUSARs. - Assist with case receipt, triage, data entry, MedDRA and WHO Drug coding, follow‑up activities, and quality checks within safety databases. - Support expedited and local ICSR submissions under supervision. - Assist with reconciliation of safety data with clinical databases. - Support global and local literature monitoring activities. - Maintain and update Drug Safety documentation, trackers, and project files in line with internal procedures. - Provide administrative and operational support to the Global Drug Safety team, including mailbox monitoring and document management. - Support compliance monitoring, reporting activities, and internal process adherence. - Collaborate with cross‑functional teams and external partners as required. Qualifications - Bachelor’s degree in pharmaceutical sciences, life sciences, medicine, or a related field. - 1–3 years of experience in Drug Safety, Pharmacovigilance, or a medical environment, including case processing and regulatory submissions. - Experience in safety case processing within both clinical trial and post‑marketing settings is required. - Basic understanding of Drug Safety regulations and guidelines, including ICH, GVP, GCP, and CIOMS. - Experience or familiarity with safety databases is an advantage. - Fluent written and spoken English. - Strong attention to detail, organizational skills, and willingness to learn. - A collaborative team player with a positive and proactive attitude. Benefits - Work remotely while contributing to a global life sciences consultancy. - Lead quality operations that directly influence patient safety and regulatory compliance. - Collaborate in a multicultural, inclusive, and innovative environment. - Enjoy opportunities for career progression, professional development, and international exposure. - Flexible Work Options: Remote working flexibility to support your lifestyle. - Generous Time Off: Enjoy 5 weeks of holiday plus national holidays and 3 personal days to recharge. - Home Office Support: Get support to create a productive home office setup. - Bonuses: Benefit from an annual bonus program, spot bonuses, and employee-nominated recognition. Company Description At Arriello, we provide Pharmacovigilance, Quality & Compliance, and Regulatory Affairs services to global pharmaceutical and life sciences companies, helping them meet regulatory requirements and protect patient safety. We are a growing business with a collaborative culture focused on high‑quality delivery, continuous improvement, and giving people the space to do their best work. Our values guide how we work: - Inclusive – We value fairness, respect, and learning from one another. - Dedicated – We deliver practical, client‑focused solutions. - Innovative – We work together to find better ways forward. - Passionate – We build strong relationships and care about the quality of what we do.
• Gather claim data and manage low to mid-level workers compensation claims to full duty Return to work • Facilitate appropriate treatment services efficiently, within required Ohio BWC Guidelines for compliance, company standards, industry best practices and/or client specific requirements • Obtain expected elements for subsequent EDI to the Bureau of Workers Compensation (BWC) • Manage medical-only and low- to mid-level lost-time workers compensation claims under close supervision • Process workers compensation claims reviewing receipt of compensation; Treatment plans; facilitating services; collaborating with all claim parties with updates and changes • Verify return to work documentation through telephonic and written communications and records return to work dates appropriately in system(s) • Manage claims in close collaboration with Claims Management Team • Support other claims management staff with larger or more complex claims as necessary • Make referral for case management and/or utilization management when work status changes due to functional limitations/medical instability • Document communications and claims management appropriately in system(s) • Respond to all inquiries within one (1) business day • Maintain knowledge of BWC rules and laws, workers compensation process, and CHS policies and procedures • Maintain professional client relationships • Meet and maintain productivity and quality expectations
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