Executive Medical Director, Clinical Development Nephrology

Department:

Location:

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 in rare for life. We continue to courageously forge new paths as we move toward a common goal of elevating science and service for rare patients.

Position Summary:

We are seeking an experienced and strategic Executive Director, Clinical Development to lead the clinical development strategy for one or more programs in rare diseases. This leader will serve as the cross-functional project leader for assigned program(s), partnering closely with Research, Translational Medicine, Regulatory, Biometrics, Clinical Operations, Medical Affairs, Commercial, and Program Management.

In this role, you will be accountable for shaping and executing development strategy from early clinical development through late-stage planning, with a strong focus on scientifically rigorous, patient-centered, and operationally feasible development plans in rare renal indications. Reporting to the SVP of Clinical Development & Clinical Pharmacology, you will play a visible leadership role across the organization and contribute meaningfully to portfolio and governance decisions in a collaborative environment.

Responsibilities:

Clinical Development Leadership

• Lead the overall clinical development strategy for assigned program(s) as a key contributor to indication strategy, target product profile, clinical positioning, and lifecycle planning.

• Serve as the project lead for clinical programs, integrating nonclinical, translational, biomarker, safety, regulatory, and competitive insights into development plans.

• Design and oversee clinical studies across phases, including protocol concept, eligibility criteria, endpoints, safety monitoring, dose selection, and statistical considerations.

• Provide leadership for study conduct, including protocol deviation review and data interpretation.

• Lead analysis and interpretation of clinical data and author or review key documents including protocols, IBs, CSRs, abstracts, manuscripts, and health authority briefing materials.

• Partner with Biometrics to define analysis strategy and ensure clinically meaningful interpretation of efficacy, safety, PK/PD, and biomarker data.

Program and Project Leadership

• Serve as the project leader for assigned development program(s), driving cross-functional alignment on program goals, timelines, risks, decision points, and resource needs.

• Lead core team meetings and represent the program at governance forums, providing clear recommendations grounded in data, development risk, and strategic fit.

• Build integrated development plans in collaboration with cross-functional partners and ensure disciplined execution against milestones.

• Identify program risks early and develop mitigation strategies spanning clinical, regulatory, operational, and portfolio considerations.

• Drive scenario planning and decision analyses to support stage-gate and investment decisions.

Regulatory and External Leadership

• Contribute to global regulatory strategy and represent Clinical Development in interactions with regulatory agencies, including FDA, EMA, and other health authorities.

• Help prepare for and participate in key regulatory meetings, including end-of-Phase 2 and other milestone interactions.

• Build and maintain relationships with academic experts, investigators, patient advocacy groups, and other external stakeholders in nephrology and rare disease.

• Support due diligence and business development activities, including assessment of external assets in nephrology or adjacent rare disease areas.

Cross-Functional and Organizational Leadership

• Partner closely with Clinical Operations to ensure study designs are executable and enrollment strategies are realistic for rare disease settings.

• Collaborate with Non-Clinical teams to incorporate mechanistic and disease-relevant endpoints into development programs.

• Productively interface with Clinical Pharmacology, Pharmacovigilance, CMC, HEOR, Medical Writing, and additional project functional leads not previously listed.

• Work with Medical Affairs and Commercial colleagues to align development plans with future evidence-generation needs and patient/community insights.

• Mentor junior project team members and contribute to building a high-performing clinical development organization.

• Model strong enterprise leadership, balancing program advocacy with portfolio-level thinking.

Education/Experience Requirements:

• MD, DO, or equivalent medical degree required; advanced scientific training may be considered in combination with substantial relevant industry leadership experience.

• 10+ years of biotechnology and/or pharmaceutical industry experience in clinical development, with progressive leadership responsibility.

• Prior experience leading clinical programs in nephrology, rare disease, or closely related therapeutic areas strongly preferred.

• Demonstrated experience serving as a program or project leader in a cross-functional drug development environment.

• Strong understanding of clinical trial design, dose selection, safety assessment, endpoint strategy, and interpretation of complex clinical datasets.

• Experience with regulatory submissions and health authority interactions.

• Track record of leading development strategy through major inflection points such as IND, proof-of-concept, end-of-Phase 2, and/or registrational planning.

• Deep appreciation for the unique challenges of rare disease development, including small populations, site selection, natural history, endpoint selection, and patient engagement.

• Excellent communication and influence skills, with the ability to synthesize complex issues for senior leaders and governance bodies.

Preferred Experience:

• Direct experience in rare kidney diseases, including inherited, glomerular, complement-mediated, or other orphan renal disorders.

• Experience with biomarkers, translational medicine, and precision medicine approaches relevant to renal disease.

• Experience in global development and multinational clinical trials.

• Prior people management experience is a plus, though not required for candidates with strong matrix leadership skills.

• Familiarity with pediatric and adolescent development considerations in rare disease is desirable, depending on program scope.

Additional Skills/Experience/Requirements:

• The ideal candidate will embody Travere's core values: Courage, Community Spirit, Patient Focus and Teamwork

• Driven, intelligent, passionate about making a difference for patients with rare diseases

• Strong interpersonal and organizational skills and excellent verbal and written communication skills

• Ability to work effectively in a multidisciplinary team to cultivate an inclusive environment of respectful, open, and honest dialogue and to foster a robust sharing of ideas and creative problem solving

• Demonstrated ability to review, interpret and present complex scientific data

• Well-organized with the ability to multi-task, prioritize, and manage shifting responsibilities in a dynamic, cross-functional teamwork environment

• Excellent collaboration skills with strong attention to detail and the ability to manage complexity and challenges

• Ability to adapt to modification and changes to project plans, demonstrating flexibility to implement new strategies and tactics to accommodate these changes

• Ability to travel domestically and internationally (up to 20 to 25%)

• All positions have an essential job function to be able to perform face to face work with colleagues and/or onsite in San Diego. No role is expected to be 100% remote

Travere is an EEO/AA/Veteran/Disability Employer

Total Rewards Offerings:
Travere provides comprehensive total rewards offerings that demonstrate our commitment as a diverse, equitable, people-centric, and pay-for-performance organization.

Benefits: Our benefits include premium health, financial, work-life and well-being offerings for eligible employees and dependents, wellness and employee support programs, life insurance, disability, retirement plans with employer match and generous paid time off.

Compensation: Our competitive compensation package includes a combination of both cash compensation (base pay and short-term incentive) and long-term incentive compensation (company stock), designed to recognize, retain, and reward employees.

Target Base Pay Range:

*This information is current as of the date of this posting and may be modified in the future. Actual pay offered to a candidate will depend on a variety of factors including the candidate's experience, education, skills, and location.

Travere will accept applications on an ongoing basis until a candidate is selected for the position.

Travere Therapeutics, Inc. is an EEO/AA/Veteran/Disability Employer.

If you require a reasonable accommodation to complete the application or interview process, please contact us by sending an email to accommodations@travere.com. Please note that this email address is to be used exclusively to request an accommodation with the online application, interview or hiring process only. Travere HR will not reply to emails sent to this address for any other reason.