Title: Compliance Manager, Compliance Admin, Full-Time, Baptist Jacksonville Hybrid - 1-2 days onsite locations Baptist Jacksonville (Downtown) time type Full time Baptist Health is hiring a Compliance Manager to join our Corporate Compliance team at Baptist Medical Center Jacksonville in Jacksonville, FL. This is a full-time hybrid opportunity, with the flexibility to work remotely 1–2 days per week. The Corporate Compliance team plays a critical role in supporting Baptist Health's commitment to ethical business practices, regulatory compliance, and organizational integrity. This role is ideal for an experienced compliance professional who thrives in a collaborative environment and is passionate about risk mitigation, regulatory oversight, and continuous program improvement. The Compliance Manager is central to day-to-day compliance operations, ensuring the organization remains proactive, responsive, and aligned with regulatory expectations. Compliance Manager Job Responsibilities: - Manage and oversee investigations, issue tracking, and follow-up activities related to compliance matters - Monitor key compliance program initiatives, ensuring effectiveness and regulatory alignment - Coordinate and support compliance training and education programs across the organization - Maintain and update compliance-related policies and procedures to reflect regulatory changes and organizational priorities - Oversee compliance hotline activities, including intake, investigation tracking, and reporting - Manage Conflict of Interest (COI) and Code of Conduct (COC) processes and related compliance activities - Monitor and support Open Payments reporting requirements and regulatory compliance obligations - Track and communicate regulatory changes, assessing potential organizational impact and recommending actions - Collaborate with operational leaders to identify and mitigate compliance risks - Support ongoing compliance program development and continuous improvement initiatives Compliance Manager Experience: - 3-5 Years Healthcare Compliance Experience Required Compliance Manager Education & Credential Requirements: - Bachelor of Arts/Science (BA/BS) - Master of Health Administration - Master of Business Administration - Certified Clinical Research Professional (CCRP) (Preferred) - Clinical Research Coordinator Certification, CRC (Preferred) - Certified in Healthcare Compliance, CHC (Preferred) Apply technical, analytical, and problem-solving skills to manage the day to day facility compliance operations. Primary Location: Downtown - Southbank Building 2

• Conduct research and deliver strategic advice for risk management leaders • Develop understanding of client requirements for successful risk management • Conduct primary research on risk management capabilities • Define the future of risk management • Collaborate with research teams to develop comprehensive research portfolio • Write and create multiple research projects annually • Consult with clients to apply Forrester’s research • Build industry presence as a speaker and thinker

• Overall activities include handling of internal and external customer compliance trade requests, processing of documentation related to US imports, free trade agreement solicitation and analysis and other trade compliance related matters • Analyze opportunities for, and assist with, submission of Section 301 exclusions • Provide support on other trade remedies such as Antidumping and Countervailing duties, Section 201, Section 232 • Evaluate qualification for Free Trade Act, Country of Origin/Sourcing analysis (Substantial Transformation) • Research complex problems involving HTS classification, assists, country of origin, marking, and valuation • Manage inquiries from US Customs, including CBP Forms 28 & 29 • Execute and oversee Post Summary Corrections, including Prior Disclosures • Review opportunities for duty minimization (tariff engineering, FTZ, CBMA etc) • Conduct training, risk assessments and internal audits • Administer & file duty drawback claims • Development of Supply Chain Safety programs, such as C-TPAT and ongoing support of C-TPAT initiatives to maintain C-TPAT approval • Monitor proposed changes in customs/trade regulations and assess the impact of these proposed changes • Drive improvements and efficiencies of established Trade processes • Support compliance audits & liaison between FTZ consultants, trade attorneys upon request

Role Description Our clinical activities are growing rapidly, and we are currently seeking a full-time home-based Regulatory Submissions Coordinator. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. - Prepare, review, and file clinical trial applications to domestic regulatory agencies; - Prepare and submit responses to queries and amendments to clinical trial applications; - Ensure submissions comply with applicable regulations and guidance documents; - Advise sponsors and internal stakeholders on changing regulations and compliance requirements; - Track submissions and ensure timely filing of documents. Qualifications - Minimum Bachelor's degree in life sciences; - At least one year of work experience as a Regulatory Submissions Coordinator for European regulation (CTR); - Excellent organization and communication skills; - Knowledge of Microsoft® Office; - Hands-on experience preparing, reviewing, and submitting regulatory documentation; - Greek (mother tongue) and very good knowledge of English. Benefits - Flexible work environment; - Competitive compensation and benefits package; - Competitive PTO packages; - Structured career paths with opportunities for professional growth; - Company-sponsored employee appreciation events; - Employee health and wellness initiatives. Company Description Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.