Travere Therapeutics
Travere Therapeutics is a biopharmaceutical company committed to identifying, developing, and delivering life-changing therapies for people living with rare diseases, particularly those related to rare kidney and metabolic disorders. The company has a strong focus on advancing science in these fields, with a pipeline that includes treatments for conditions such as IgA nephropathy and focal segmental glomerulosclerosis. With the full U. S. FDA approval of its non-immunosuppressive treatment for IgA nephropathy, Travere Therapeutics continues to set new standards of care. The company collaborates with the rare kidney disease community, including patient advocacy organizations and clinical trial investigators, to bring hope to patients with these serious conditions.
Senior Manager - Commercial Regulatory
March 14
Travere Therapeutics
Travere Therapeutics is a biopharmaceutical company committed to identifying, developing, and delivering life-changing therapies for people living with rare diseases, particularly those related to rare kidney and metabolic disorders. The company has a strong focus on advancing science in these fields, with a pipeline that includes treatments for conditions such as IgA nephropathy and focal segmental glomerulosclerosis. With the full U. S. FDA approval of its non-immunosuppressive treatment for IgA nephropathy, Travere Therapeutics continues to set new standards of care. The company collaborates with the rare kidney disease community, including patient advocacy organizations and clinical trial investigators, to bring hope to patients with these serious conditions.
📋 Description
• Responsible for assisting with labeling development and Regulatory advertising and promotion • Works closely with internal stakeholders to ensure alignment with strategies and regulatory guidance • Represents Regulatory Affairs on key review committees • Ensures compliance with market commitments and regulatory standards
🎯 Requirements
• Bachelor’s degree in related Life Sciences discipline • Minimum 7+ years of regulatory and/or related experience within the Biotech or Pharmaceutical industry • Knowledge and understanding of pharmaceutical drug development and regulations pertaining to labeling • Demonstrated ability to understand implications of label changes on pending and approved labels
🏖️ Benefits
• Premium health offerings • Financial offerings • Work-life and well-being offerings for eligible employees and dependents • Wellness and employee support programs • Life insurance • Disability • Retirement plans with employer match • Generous paid time off
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