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Science & Research
Researcher / Research Associate
Riverdale, GA

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Professional Case Management

Principal Clinical Research Scientist - Home Healthcare

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Job Description

Principal Clinical Research Scientist -
Home Healthcare Date Posted:
1 October 2026
Closing Date:
October 31, 2026
Recruiter:
Professional Case Management Location:
Riverdale, Georgia Salary:
USD205,000
to
USD250,000
Job Type & Industry:
Technology Risk, Healthcare & Pharmaceutical, Scientific & Research Contract Type:
Permanent Job Reference:
2996438738-2 Apply for this job now Job Description Professional Case Management is seeking a Principal Investigator to lead clinical and scientific research within our Healthcare & Medical organization. In this Scientific Research & Development role, you will design and oversee studies focused on complex medical needs, ensuring regulatory and ethical compliance. Responsibilities include protocol development, data analysis, report authorship, and collaboration with interdisciplinary care teams. You will mentor researchers, contribute to evidence-based best practices, and support innovation in in-home care for former energy workers and their families. Join a collaborative, compassionate culture with robust training and clear pathways for career growth while making a direct impact on patient outcomes. Responsibilities Provide scientific and clinical leadership for in-home healthcare initiatives serving former energy workers and their families Design, implement, and oversee clinical protocols, quality-improvement projects, and outcomes-focused studies Ensure full compliance with ethical standards, Good Clinical Practice, and all applicable regulatory and payer requirements Supervise and monitor clinical aspects of projects, including patient safety, adverse event review, and data integrity Collaborate with nurses, case managers, and allied health professionals to ensure consistent, patient-centered protocol implementation Review and interpret clinical data and outcomes, translating findings into evidence-based recommendations for practice improvement Support the informed consent process and maintain high standards of documentation and record-keeping Provide clinical consultation for complex cases and serve as a subject-matter expert on the needs of former energy workers Educate and mentor clinical staff on evidence-based practice, new guidelines, and protocol updates Present findings and recommendations to organizational leadership and external stakeholders, contributing to strategic planning and service development Required Skills Clinical research design Protocol development Regulatory compliance (FDA, IRB, GCP) Data analysis and interpretation Clinical project management Risk management and quality assurance Budgeting and resource allocation Electronic health record (EHR) use Clinical documentation Patient assessment and monitoring Informed consent process Stakeholder communication Scientific writing and publication Leadership and team development Presentation of scientific findings