Executive Medical Director Clinical Development
Executive Medical Director Clinical Development
Posted on :
11-03-2025
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1 Vacancy
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Monthly Salary
Not Disclosed
Salary Not Disclosed
Vacancy
1 Vacancy
Posted on :
11-03-2025
Job Description
Job Title: Executive Medical Director Clinical Development
Job Location: United States
Job Location Type: Remote
Job Contract Type: Fulltime
Job Seniority Level: Executive
Department:
106750 Clinical Dev NonRenal
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 fastpaced environment and share in our mission – to identify develop and deliver lifechanging 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:
The Executive Medical Director Clinical Development (nonrenal) is responsible for providing overall clinical and scientific oversight and leadership for Travere’s rare metabolic development programs and clinical research projects across Phases 14. This will include an exciting highvisibility Phase 3 program in a rare metabolic disease and may include other therapeutic areas as the company expands its pipeline. This position will report to the SVP Clinical Development and Clinical Pharmacology.
This experienced clinical leader will work collaboratively with all functions including the being a member of development Program Strategy Team (PST) with the purpose to develop and deliver a clinical development strategy tailored to the disease that is efficient and of high scientific quality.
Additional responsibilities include developing relationships with leading key opinion leaders acting as subject matter expert for additional programs provide medical support as needed for clinical trials marketed products pharmacovigilance and provide medical/scientific expertise as needed for business development efforts.
Responsibilities:
Travere provides comprehensive total rewards offerings that demonstrate our commitment as a diverse equitable peoplecentric and payforperformance organization.
Benefits: Our benefits include premium health financial worklife and wellbeing 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 shortterm incentive) and longterm incentive compensation (company stock) designed to recognize retain and reward employees.
Target Base Pay Range:
$285000.00 $385000.00
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 . 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.
106750 Clinical Dev NonRenal
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 fastpaced environment and share in our mission – to identify develop and deliver lifechanging 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:
The Executive Medical Director Clinical Development (nonrenal) is responsible for providing overall clinical and scientific oversight and leadership for Travere’s rare metabolic development programs and clinical research projects across Phases 14. This will include an exciting highvisibility Phase 3 program in a rare metabolic disease and may include other therapeutic areas as the company expands its pipeline. This position will report to the SVP Clinical Development and Clinical Pharmacology.
This experienced clinical leader will work collaboratively with all functions including the being a member of development Program Strategy Team (PST) with the purpose to develop and deliver a clinical development strategy tailored to the disease that is efficient and of high scientific quality.
Additional responsibilities include developing relationships with leading key opinion leaders acting as subject matter expert for additional programs provide medical support as needed for clinical trials marketed products pharmacovigilance and provide medical/scientific expertise as needed for business development efforts.
Responsibilities:
- Clinical development lead for assigned development programs as part of the Program Strategy Team (PST) and represents the program to executive leadership and study team members.
- Responsible for leading the development of protocols and clinical/scientific strategy across Phase 14.
- Understanding of the development and regulatory strategy (from preIND to NDA/BLA) and devices (Human Factor studies) to provide clinical and scientific insights as part of the PST.
- Understanding and knowledge of the rare metabolic and genetic disease areas as well as the future landscape and treatment paradigm in order to provide strategic input into future development needs biometrics analyses publications and core presentations.
- Partners with Biometrics to plan data entry analysis and interprets in collaboration with biostatistics the data results for the PST and Medical Affairs colleagues.
- Supports the recruitment/screening/selection of competent investigators in collaboration with Clinical Operations; assures that Good Clinical Practices (GCPs) are followed; assures timely completion of studies; monitors data for safety and efficacy trends by reviewing clinical data; and authors clinical reports upon completion or termination of studies (in cooperation with statistical staff/consultants).
- Accountable for preparing clinical portions of protocols investigator brochures medical reports efficacy and safety summaries scientific rationales and benefit/risk ratios.
- Lead and mentor Clinical Development staff consultants and vendor medical monitor to foster a highperformance culture within the Clinical Development department.
- Proactively establishes and maintains relationships with stakeholders i.e. alliance partners external companies investigators and key opinion leaders.
- Plays a key leadership role in Health Authority interactions and development of regulatory documents.
- Attend and present at investigator meetings and site initiation visits as applicable.
- Works crossfunctionally with medical affairs and prepares manuscripts posters and other scientific communications and conducts presentations at scientific meetings.
- Understanding of governance and ability to represent the programs and key decisions at crossfunctional governance meetings.
- M.D. or M.D./Ph.D. degree or equivalent required. Equivalent combination of education and applicable job experience may be considered.
- 10 years of experience in clinical research including the design and of clinical trials preferably within a pharmaceutical or biotech environment. 6 years leadership experience. Strong academic experience will be considered.
- Demonstrated ability to lead crossfunctional teams in a matrix environment.
- Metabolics/genetics and/or rare disease experience and NDA/BLA submissions is strongly preferred.
- 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
- Experiences with devices and human factors studies preferred
- 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
- Wellorganized with the ability to multitask prioritize and manage shifting responsibilities in a dynamic crossfunctional 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 domestic and internationally (up 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 provides comprehensive total rewards offerings that demonstrate our commitment as a diverse equitable peoplecentric and payforperformance organization.
Benefits: Our benefits include premium health financial worklife and wellbeing 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 shortterm incentive) and longterm incentive compensation (company stock) designed to recognize retain and reward employees.
Target Base Pay Range:
$285000.00 $385000.00
- 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 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 . 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.
https://lifelancer/jobs/view/1b42e70ca54ca84a55775cf07d7bb26c
Employment Type
Full Time
Key Skills
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