- Sumitomo Pharma (Baton Rouge, LA)
- …(SME) on behalf of PVRM for: Study Protocols, Informed Consent Forms (ICF), Safety Management Plans (SMP), Clinical Study Reports (CSR), Investigator's ... data, expedited individual and aggregate periodic safety reporting, signal generation, safety evaluation and risk management and mitigation strategies.… more
- Datavant (Baton Rouge, LA)
- …of product management experience in healthcare, including ownership of clinical , risk adjustment, or provider-facing solutions. + Proven leadership ... of service. This is a leadership role that combines strategic thinking, clinical product development expertise, and people management responsibilities. You'll be… more
- Datavant (Baton Rouge, LA)
- …life experiences to realize our bold vision for healthcare. As an Auditor, HCC Risk Adjustment Coder, you will review medical records to identify and code diagnoses ... using a standardized system, ensuring accurate representation of patient conditions for risk adjustment and reimbursement purposes. You will play a critical role in… more
- Veterans Affairs, Veterans Health Administration (New Orleans, LA)
- …regulatory standards and compliance requirements (FDA, Joint Commission, OSHA) Experience with risk assessment, risk management and mitigation strategies for ... policies and procedures. Incumbent must manage the recall and safety alert program for medical devices, investigate incidents to...the HTM expert for the Environment of Care Committee. Management of the quality assurance program for clinical… more
- Datavant (Baton Rouge, LA)
- …using a standardized system, ensuring accurate representation of patient conditions for risk adjustment and reimbursement purposes. You will play a critical role in ... translating clinical documentation into precise codes that reflect the complexity...ability to work in a remote environment, and time management skills. + Working knowledge of the business use… more
- Datavant (Baton Rouge, LA)
- …in a standardized system, ensuring accurate representation of patient conditions for risk adjustment and reimbursement purposes. You will play a critical role in ... translating clinical documentation into precise codes that reflect the complexity...ability to work in a remote environment and time management skills + Working knowledge of the business use… more
- Ochsner Health (New Orleans, LA)
- …evaluates, initiates, and maintains all activities related to the conduct of clinical trials in assigned area(s) of responsibility in coordination and collaboration ... to ensure understanding of the requirements of conducting and participating in clinical trials. Organizes and manages all patient care requirements. Provides patient… more
- Ochsner Health (Covington, LA)
- …job evaluates, initiates and maintains activities related to the conduct of clinical trials with the assistance and guidance of departmental staff. Communicates ... the understanding of the requirements of conducting and participating in clinical trials. Organizes and manages all documentation and regulatory submissions as… more
- Ochsner Health (New Orleans, LA)
- …job evaluates, initiates, and maintains activities related to the conduct of clinical trials with the assistance and guidance of departmental staff. Communicates ... ensure the understanding of the requirements of conducting and participating in clinical trials. Organizes and manages all patient care requirements of the company… more
- Ochsner Health (New Orleans, LA)
- …initiates, and maintains all activities related to the conduct of clinical trials. Communicates with external funding agencies and sponsors, other departments, ... ensure the understanding of the requirements of conducting and participating in clinical trials. Independently organizes and manages all patient care requirements of… more
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