Director MCVI Research & Outcomes, MCVI Research, FT, 8A-4:30P
Baptist Health is the region's largest not-for-profit healthcare organization, with 12 hospitals, over 29,000 employees, 4,500 physicians and 200 outpatient centers, urgent care facilities and physician practices across Miami-Dade, Monroe, Broward and Palm Beach counties. With internationally renowned centers of excellence in cancer, cardiovascular care, orthopedics and sports medicine, and neurosciences, Baptist Health is supported by philanthropy and driven by its faith-based mission of medical excellence. For 26 years, we've been named one of Fortune's 100 Best Companies to Work For, and in the 2025-2026 U.S. News & World Report Best Hospital Rankings, Baptist Health was the most awarded healthcare system in South Florida, earning 63 high-performing honors.
What truly sets us apart is our people. At Baptist Health, we create personal connections with our colleagues that go beyond the workplace, and we form meaningful relationships with patients and their families that extend beyond delivering care. Many of us have walked in our patients' shoes ourselves and that shared experience fuels out commitment to compassion and quality. Our culture is rooted in purpose, and every team member plays a part in making a positive impact - because when it comes to caring for people, we're all in.
At Baptist Health, we're committed to supporting our employees at every stage of their journey, both personally and professionally. Our approach is rooted in a "grow our own" philosophy, designed to help our team members build meaningful, long-term careers with us, supported by benefits that make a real difference, including:
Description
Provides strategic, operational, financial, and regulatory oversight for all cardiovascular clinical trial activities across the health system's inpatient hospitals and outpatient ambulatory clinics, including standardization of clinical trial workflows, patient recruitment strategies, and data collection protocols. Manages clinical research coordinators, interfaces directly with practicing clinicians, and ensures that research activities integrate seamlessly with standard patient care operations. Evaluates incoming trial protocols for operational feasibility, resource availability, and patient accrual potential across the entire healthcare system network. Drives financial sustainability while expanding patient access to cutting-edge clinical therapies. Ensures strict regulatory compliance with FDA and HIPAA standards and aligns trial operations between health system and satellite clinics. Partners with Principal Investigators (PIs), department chairs, and medical directors to support investigator-initiated studies and industry-sponsored trial portfolios.
Qualifications:
Provides strategic, operational, financial, and regulatory oversight for all cardiovascular clinical trial activities across the health system's inpatient hospitals and outpatient ambulatory clinics, including standardization of clinical trial workflows, patient recruitment strategies, and data collection protocols. Manages clinical research coordinators, interfaces directly with practicing clinicians, and ensures that research activities integrate seamlessly with standard patient care operations. Evaluates incoming trial protocols for operational feasibility, resource availability, and patient accrual potential across the entire healthcare system network. Drives financial sustainability while expanding patient access to cutting-edge clinical therapies. Ensures strict regulatory compliance with FDA and HIPAA standards and aligns trial operations between health system and satellite clinics. Partners with Principal Investigators (PIs), department chairs, and medical directors to support investigator-initiated studies and industry-sponsored trial portfolios.Degrees:
• Masters
Additional Qualifications:
• Advanced scientific or clinical degree (Ph.D., M.D., D.O.) preferred.
• 10+ years of progressively responsible experience in clinical research operations, with at least 5 years in a dedicated leadership/managerial role in a pharmaceutical, biotech, or healthcare organization.
• Active certification as a Certified Clinical Research Professional (CCRP via SOCRA) or Certified Clinical Research Coordinator/Manager (CCRC/CCRM via ACRP) preferred.
• Comprehensive knowledge of FDA regulations, Department of Health and Human Services (DHHS) policies, ICH-GCP (Good Clinical Practice) guidelines, and Medicare research billing rules.
• Advanced proficiency with Clinical Trial Management Systems (CTMS) and enterprise EHR platforms.
• Exceptional negotiation skills with a deep understanding of clinical trial agreements (CTAs) and corporate budgeting templates.
• Proven track record managing diverse therapeutic portfolios, including high-acuity specialties (e.g., Cardiovascular, Oncology) and outpatient preventative registries.
• Must possess medical or bioscientific, business, grant/promotional writing and presentation skills.
• Demonstrates strong planning, management, organization and analytical skills.
• Requires extensive amount of initiative, analytical and evaluation efforts and constructive thinking to develop alternatives for resolution to frequently changing and difficult situations.
Minimum Required Experience: 10 YearsDegrees:
• Masters
Additional Qualifications:
• Advanced scientific or clinical degree (Ph.D., M.D., D.O.) preferred.
• 10+ years of progressively responsible experience in clinical research operations, with at least 5 years in a dedicated leadership/managerial role in a pharmaceutical, biotech, or healthcare organization.
• Active certification as a Certified Clinical Research Professional (CCRP via SOCRA) or Certified Clinical Research Coordinator/Manager (CCRC/CCRM via ACRP) preferred.
• Comprehensive knowledge of FDA regulations, Department of Health and Human Services (DHHS) policies, ICH-GCP (Good Clinical Practice) guidelines, and Medicare research billing rules.
• Advanced proficiency with Clinical Trial Management Systems (CTMS) and enterprise EHR platforms.
• Exceptional negotiation skills with a deep understanding of clinical trial agreements (CTAs) and corporate budgeting templates.
• Proven track record managing diverse therapeutic portfolios, including high-acuity specialties (e.g., Cardiovascular, Oncology) and outpatient preventative registries.
• Must possess medical or bioscientific, business, grant/promotional writing and presentation skills.
• Demonstrates strong planning, management, organization and analytical skills.
• Requires extensive amount of initiative, analytical and evaluation efforts and constructive thinking to develop alternatives for resolution to frequently changing and difficult situations.
Minimum Required Experience: 10 Years
What truly sets us apart is our people. At Baptist Health, we create personal connections with our colleagues that go beyond the workplace, and we form meaningful relationships with patients and their families that extend beyond delivering care. Many of us have walked in our patients' shoes ourselves and that shared experience fuels out commitment to compassion and quality. Our culture is rooted in purpose, and every team member plays a part in making a positive impact - because when it comes to caring for people, we're all in.
At Baptist Health, we're committed to supporting our employees at every stage of their journey, both personally and professionally. Our approach is rooted in a "grow our own" philosophy, designed to help our team members build meaningful, long-term careers with us, supported by benefits that make a real difference, including:
- Career growth and development opportunities, with clear pathways and ongoing support
- Comprehensive health and wellness resources that go beyond traditional benefits
- A wellness program that can help employees eliminate their medical plan deductible, reducing out-of-pocket healthcare costs
- Tuition reimbursement to support continued learning and advancement
- And so much more
Description
Provides strategic, operational, financial, and regulatory oversight for all cardiovascular clinical trial activities across the health system's inpatient hospitals and outpatient ambulatory clinics, including standardization of clinical trial workflows, patient recruitment strategies, and data collection protocols. Manages clinical research coordinators, interfaces directly with practicing clinicians, and ensures that research activities integrate seamlessly with standard patient care operations. Evaluates incoming trial protocols for operational feasibility, resource availability, and patient accrual potential across the entire healthcare system network. Drives financial sustainability while expanding patient access to cutting-edge clinical therapies. Ensures strict regulatory compliance with FDA and HIPAA standards and aligns trial operations between health system and satellite clinics. Partners with Principal Investigators (PIs), department chairs, and medical directors to support investigator-initiated studies and industry-sponsored trial portfolios.
Qualifications:
Provides strategic, operational, financial, and regulatory oversight for all cardiovascular clinical trial activities across the health system's inpatient hospitals and outpatient ambulatory clinics, including standardization of clinical trial workflows, patient recruitment strategies, and data collection protocols. Manages clinical research coordinators, interfaces directly with practicing clinicians, and ensures that research activities integrate seamlessly with standard patient care operations. Evaluates incoming trial protocols for operational feasibility, resource availability, and patient accrual potential across the entire healthcare system network. Drives financial sustainability while expanding patient access to cutting-edge clinical therapies. Ensures strict regulatory compliance with FDA and HIPAA standards and aligns trial operations between health system and satellite clinics. Partners with Principal Investigators (PIs), department chairs, and medical directors to support investigator-initiated studies and industry-sponsored trial portfolios.Degrees:
• Masters
Additional Qualifications:
• Advanced scientific or clinical degree (Ph.D., M.D., D.O.) preferred.
• 10+ years of progressively responsible experience in clinical research operations, with at least 5 years in a dedicated leadership/managerial role in a pharmaceutical, biotech, or healthcare organization.
• Active certification as a Certified Clinical Research Professional (CCRP via SOCRA) or Certified Clinical Research Coordinator/Manager (CCRC/CCRM via ACRP) preferred.
• Comprehensive knowledge of FDA regulations, Department of Health and Human Services (DHHS) policies, ICH-GCP (Good Clinical Practice) guidelines, and Medicare research billing rules.
• Advanced proficiency with Clinical Trial Management Systems (CTMS) and enterprise EHR platforms.
• Exceptional negotiation skills with a deep understanding of clinical trial agreements (CTAs) and corporate budgeting templates.
• Proven track record managing diverse therapeutic portfolios, including high-acuity specialties (e.g., Cardiovascular, Oncology) and outpatient preventative registries.
• Must possess medical or bioscientific, business, grant/promotional writing and presentation skills.
• Demonstrates strong planning, management, organization and analytical skills.
• Requires extensive amount of initiative, analytical and evaluation efforts and constructive thinking to develop alternatives for resolution to frequently changing and difficult situations.
Minimum Required Experience: 10 YearsDegrees:
• Masters
Additional Qualifications:
• Advanced scientific or clinical degree (Ph.D., M.D., D.O.) preferred.
• 10+ years of progressively responsible experience in clinical research operations, with at least 5 years in a dedicated leadership/managerial role in a pharmaceutical, biotech, or healthcare organization.
• Active certification as a Certified Clinical Research Professional (CCRP via SOCRA) or Certified Clinical Research Coordinator/Manager (CCRC/CCRM via ACRP) preferred.
• Comprehensive knowledge of FDA regulations, Department of Health and Human Services (DHHS) policies, ICH-GCP (Good Clinical Practice) guidelines, and Medicare research billing rules.
• Advanced proficiency with Clinical Trial Management Systems (CTMS) and enterprise EHR platforms.
• Exceptional negotiation skills with a deep understanding of clinical trial agreements (CTAs) and corporate budgeting templates.
• Proven track record managing diverse therapeutic portfolios, including high-acuity specialties (e.g., Cardiovascular, Oncology) and outpatient preventative registries.
• Must possess medical or bioscientific, business, grant/promotional writing and presentation skills.
• Demonstrates strong planning, management, organization and analytical skills.
• Requires extensive amount of initiative, analytical and evaluation efforts and constructive thinking to develop alternatives for resolution to frequently changing and difficult situations.
Minimum Required Experience: 10 Years