Travere Therapeutics

Department: 107000 Regulatory Location: San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease. At Travere Therapeutics, we recognize that our exceptional employees are vital to our success. We are a dedicated team focused on meeting the unique needs of rare patients. Our work is rewarding - both professionally and personally - because we are making a difference. We are passionate about what we do. We are seeking talented individuals who will thrive in our collaborative, diverse, fast‑paced environment and share in our mission - to identify, develop and deliver life‑changing therapies to people living with rare disease. We stick by our values centered on patients, courage, community, and collaboration to pursue our vision of becoming a leading biopharmaceutical company dedicated to the delivery of innovation and hope to patients in the global rare disease community. At Travere Therapeutics, we are...

Department: 107000 Regulatory Location: San Diego, USA - Remote Position Summary The Associate Director, Medical Writing is responsible for oversight and authoring (if needed) of regulatory submissions (Common Technical Documents [CTD]), as well as other regulatory, clinical, and safety documents, including but not limited to protocols and amendments, clinical study reports (CSRs), Investigator's Brochures (IBs), and Periodic Safety Update Reports (PSURs). This position contributes to the strategy of document development, overall project management during drafting, reviewing, and approval cycles of regulatory submissions and other documents, and may oversee other writers contributing to the submission. The role ensures documents are compliant with company-specific medical writing standards, are completed on time and on budget, and are ready for submission to global, regional, and local regulatory authorities, supporting projects across all phases of clinical development and...

Department: 107000 Regulatory Location: San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease. At Travere Therapeutics, we recognize that our exceptional employees are vital to our success. We are a dedicated team focused on meeting the unique needs of rare patients. Our work is rewarding - both professionally and personally - because we are making a difference. We are passionate about what we do. We are seeking talented individuals who will thrive in our collaborative, diverse, fast‑paced environment and share in our mission - to identify, develop and deliver life‑changing therapies to people living with rare disease. We stick by our values centered on patients, courage, community, and collaboration to pursue our vision of becoming a leading biopharmaceutical company dedicated to the delivery of innovation and hope to patients in the global rare disease community. At Travere Therapeutics, we are...

Travere Therapeutics seeks an Associate Director, Medical Writing responsible for overseeing regulatory submissions and authoring critical documents. This role leads medical writing projects and ensures compliance with regulatory standards while mentoring junior writers. Candidates should have a Master’s degree and a minimum of 6 years in medical writing within the biopharmaceutical industry. Strong writing, editing, and project management skills are essential. Remote working options are available, with a competitive salary range of $150,000 - $195,000. #J-18808-Ljbffr

Travere Therapeutics in Washington is seeking an Associate Director, Medical Writing. The role involves overseeing and authoring regulatory submissions and other key documents, ensuring compliance with medical writing standards. The ideal candidate should have a Master's Degree in Life Science and significant medical writing experience in a biopharmaceutical setting. This position offers flexible remote work options while requiring on-site collaboration for key functions. Comprehensive rewards include competitive pay ranging from $150,000 to $195,000, health benefits, and supportive work-life balance programs. #J-18808-Ljbffr

Travere Therapeutics is looking for an Associate Director, Medical Writing who will oversee regulatory submissions and lead medical writing projects. The ideal candidate will have a Master's degree in Life Sciences, with at least six years of progressively responsible experience in medical writing, especially in the biopharmaceutical sector. This role involves collaboration with cross-functional teams, ensuring that all documents meet quality and regulatory standards. A competitive compensation package is available, along with comprehensive benefits. #J-18808-Ljbffr

Department: 107000 Regulatory Location: San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease. At Travere Therapeutics, we recognize that our exceptional employees are vital to our success. We are a dedicated team focused on meeting the unique needs of rare patients. Our work is rewarding - both professionally and personally - because we are making a difference. We are passionate about what we do. We are seeking talented individuals who will thrive in our collaborative, diverse, fast‑paced environment and share in our mission - to identify, develop and deliver life‑changing therapies to people living with rare disease. We stick by our values centered on patients, courage, community, and collaboration to pursue our vision of becoming a leading biopharmaceutical company dedicated to the delivery of innovation and hope to patients in the global rare disease community. At Travere Therapeutics, we are...

Travere Therapeutics is seeking an Associate Director, Medical Writing to lead regulatory submission efforts, ensuring compliance and high-quality document delivery. This role involves oversight of medical writers and collaborating with teams throughout the product lifecycle. The ideal candidate will possess a Master's Degree and have a minimum of 6 years in medical writing. Strong skills in scientific writing and project management are essential. This position offers a competitive salary and comprehensive benefits. #J-18808-Ljbffr

Department: 107000 Regulatory Location: San Diego, USA - Remote Position Summary The Associate Director, Medical Writing is responsible for oversight and authoring (if needed) of regulatory submissions (Common Technical Documents [CTD]), as well as other regulatory, clinical, and safety documents, including but not limited to protocols and amendments, clinical study reports (CSRs), Investigator’s Brochures (IBs), and Periodic Safety Update Reports (PSURs). This position is responsible for contributing to the strategy of document development strategy, overall project management during the drafting, reviewing, and approval cycles of regulatory submissions and other documents, and may oversee other writers contributing to the submission. This position will ensure documents that are compliant with company‑specific medical writing standards, are completed on‑time and on‑budget, and are ready for submission to global, regional, and local regulatory authorities. Additionally, this...