Title: CLINICAL DIETITIAN Location: Gainesville, FL - Onsite work only, no remote Setting: Acute Care | Full-Time, Part-Time, and PRN positions available Schedule: Monday-Friday, rotating weekend schedule Requirement: RD or RD eligible, FL license Salary: $70,000-$85,000 | Based on Experience We go the extra mile for our Dietitians with benefits designed to support education, career growth, and professional success! Special perks include: - Education Reimbursement – Financial support for advanced learning - Career Advancement – Growth programs tailored to RDNs - Board Certifications – Financial rewards for obtaining specialty certifications - Relocation Assistance – Support when moving 50+ miles (based on location) - Professional Membership Dues, CDR, & Licensure Coverage – We cover your professional fees - Free CEUs – Through our nutrition education webinar series Why Choose a Career as a Compass Group Dietitian? Compass Group employs over 3,000 RDNs across the United States, making us one of the nation’s largest employers of Dietitians in a variety of settings: - - Hospitals and healthcare systems - Senior living communities - Schools and universities - Corporate wellness programs - Food service operations We offer unmatched opportunities for professional growth: - - Specialization - Leadership development - Cross-functional career paths The company has earned significant recognition, including being named one of Modern Healthcare's "Top 100 Best Places to Work in Healthcare" for five consecutive years, and appearing on Training Magazine’s Top 125 Organizations list for six straight years. At Compass Group, we prioritize your well-being, work-life balance, and career growth with a comprehensive benefits package: - Health & Wellness – Medical, dental, and vision plans for you and your family - Financial Security – Life insurance, AD&D, and disability coverage - Retirement Ready – 401(k) and retirement plans to invest in your future - Time Off – Flexible/Paid Time Off and holiday pay (varies by site/state), Paid Parental Leave, Personal Leave - Exclusive Perks – Shopping discounts, commuter benefits, and more - Wellness & Support – Employee Assistance Program, FSAs, and health programs - Protection Plans – Identity Theft Protection and pet insurance Job Summary Make a real impact as a Clinical Dietitian! You’ll provide Medical Nutrition Therapy and education in an acute care setting, working with a collaborative team to enhance patient outcomes through evidence-based nutrition care. What You’ll Do: • Clinical Nutrition Care: Perform comprehensive nutritional assessments and develop individualized care plans to promote recovery and improve health outcomes • Education: Provide guidance on nutrition and lifestyle strategies to support sustainable, long-term wellness to patients, families, staff, and the community • Evidence-Based Practice: Apply the latest research in alignment with the diet manual, company policies, and facility protocols to ensure high-quality, consistent care • Quality & Performance Improvement: Contribute to QAPI initiatives aimed at advancing patient care and clinical excellence • Collaboration & Service Excellence: Partner with the food service management team to help achieve patient satisfaction and service goals • Mentorship & Professional Development: Support the growth of staff and dietetic interns through education and training as applicable What We’re Looking For: • Registered Dietitian Nutritionist (RDN) or CDR exam eligible • Licensed Dietitian (or willing to obtain) in the state of practice as applicable • Healthcare experience preferred—new graduates with strong clinical training are encouraged to apply Why You’ll Love Working Here: • You’ll be part of an environment where your ideas are welcomed, and your growth is encouraged • You’ll have access to ongoing education, resources, development, and advancement opportunities to support your career path • You’ll have the autonomy to apply your clinical judgment while still having guidance when you need it

Role Description The Clinical Study Team Assistant (CSTA) is an essential part of the Study Team and is responsible for supporting key clinical trial tasks for assigned studies to ensure compliance with timelines, Good Clinical Practice (GCP), and SOPs. The role collaborates with global study team members and is responsible for multiple tasks that span from study start-up to study close-out which enables the efficient execution of clinical trials to high quality standards. What You Will Do: - Lead on clinical coordination tasks requiring technical depth, with a focus on quality and continuous improvement. - Key responsibilities include: - Management and oversight of Study Team shared spaces - Trial Master File (TMF) maintenance, compliance, and oversight - Analyze, interpret, and follow up on metrics - Management and oversight of Study Team on Demand (STOD) - Maintain Pfizer registries and systems as required to ensure compliance - Tracking and oversight of study information; follow up with functional lines as needed - Liaising with cross functional study team members - Initiate and coordinate the completion of study level forms and data entry into various clinical operations applications and systems - Provide study level reporting to support management of clinical trial data, clinical trial budget and timelines - Quality control of essential clinical trial documentation including components of the Clinical Study Report (CSR) and regulatory submission - Support engagement of Independent Oversight Committees - Provide support with audit and inspection readiness activities - Assist with oversight and tracking of Clinical Trial Budget spend - Provide logistical and operational support for Investigator Meetings - Coordinate the translation of documents as required - Provide status updates on key tasks and contribute to the Study Team Meetings as an active Study Team member - Provide support to study teams with system setup and maintenance - May provide support for global study team communications to sites Qualifications - 1-3 years experience with BA/BS or 1+ years experience with MA/MBA/MS - Proficient in Microsoft Office applications (Outlook, Word, PowerPoint, Excel, TEAMS) - Relevant clinical research or clinical trial experience or relevant coursework in drug development or clinical research - Science background - Experienced with clinical trial processes and applicable systems - Effective verbal and written communication skills - Ability to work independently but also as part of a larger team with limited support from supervisor - Ability to multitask and manage multiple competing priorities - Self-motivated and ability to organize tasks to ensure timelines are met and deliverables are of high quality - Knowledge of drug development process - Attention to detail evident in a disciplined approach to document review, adherence to SOPs, metrics, etc. - Good problem solving & decision-making skills Requirements - Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Benefits - Competitive base salary and performance related incentives - Health and wellbeing programmes including medical, dental, and vision coverage where applicable - Retirement and pension plans - Life assurance and disability coverage - Employee assistance programmes and wellbeing resources - Learning and development opportunities through structured training and career pathways - Benefits may vary depending on role and location. Company Description ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

Role Description You could be the one who changes everything for our 28 million members. Centene is transforming the health of our communities, one person at a time. As a diversified, national organization, you’ll have access to competitive benefits including a fresh perspective on workplace flexibility. ***POSITION IS REMOTE NATIONWIDE*** ***LOOKING FOR CANDIDATE WITH CPC OR CPMA CERTIFICATION*** - Audit medical records to identify inappropriate billing practices and recommend next steps through extensive review of claims data, medical records, corporate policy, state/federal policy, and practice standards. - Perform retrospective and prepayment reviews of medical records to identify potential abuse and fraud and inappropriate billing practices. - Investigate, analyze, and identify provider billing patterns to recommend payment based on medical records, claim history, billing codes, regulatory and state guidelines, and policies. - Prepare summary of findings and recommend next steps for providers. - Identify preventative measures and recommend changes to internal policies and procedures and/or provider practices to prevent future fraudulent and erroneous practices. - Consult investigators to identify abuse and fraud by utilizing clinical and coding expertise to analyze patterns in billing activities. - Performs other duties as assigned. - Complies with all policies and standards. Qualifications - Associate's Degree related field or equivalent experience preferred. - 2+ years related clinical experience in the field of obtained license required. - Provider education preferred. Requirements - Coding certification from an accredited organization (American Academy of Professional Coders or American Health Information Management Association), RN, LPC, LPN, LCSW, LMHC, PT, OT, or ST or related license required. Benefits - Competitive pay. - Health insurance. - 401K and stock purchase plans. - Tuition reimbursement. - Paid time off plus holidays. - Flexible approach to work with remote, hybrid, field or office work schedules. - Actual pay will be adjusted based on an individual's skills, experience, education, and other job-related factors permitted by law, including full-time or part-time status. - Total compensation may also include additional forms of incentives. - Benefits may be subject to program eligibility.

Role Description As a Senior Clinical Associate at ICON, you will oversee and support the execution of clinical trials, ensuring the highest standards of quality, compliance, and efficiency. - Lead on clinical coordination tasks requiring technical depth, with a focus on quality and continuous improvement. - Manage and coordinate clinical trial activities to ensure adherence to protocols, regulatory requirements, and project timelines. - Collaborate with cross-functional teams to address clinical trial issues, optimize processes, and ensure the effective execution of studies. - Oversee site management and monitoring to ensure data integrity and compliance with study protocols. - Provide guidance and support to clinical staff and investigators, ensuring adherence to best practices and regulatory standards. - Track and report on trial progress, identifying potential risks, and implementing strategies to mitigate challenges. Qualifications - Bachelor's degree in a relevant scientific discipline or healthcare-related field. - Significant experience in clinical trial management, with a strong understanding of clinical trial processes and regulatory requirements. - Proven ability to manage multiple projects effectively, with strong organizational and problem-solving skills. - Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders. - Detail-oriented with a proactive approach to ensuring trial success and addressing clinical challenges. Requirements - Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Benefits - Competitive base salary and performance related incentives. - Health and wellbeing programmes including medical, dental, and vision coverage where applicable. - Retirement and pension plans. - Life assurance and disability coverage. - Employee assistance programmes and wellbeing resources. - Learning and development opportunities through structured training and career pathways. - Benefits may vary depending on role and location.