Associate Director, Pharmacometrics, Clinical Pharmacology
$150k - $195kTravere Therapeutics
Department: 106750 Clinical Development 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. Position Summary The individual will be responsible for the design, leadership, and implementation of Modeling & Simulation strategies across Travere clinical programs. In this role, you will perform or supervise execution of the pharmacometrics strategy in those programs with a focus on implementing model‑informed drug development (MIDD) approaches. You will set the strategy for addressing pharmacometric issues and directly influence drug development decisions. The successful candidate will have good quantitative pharmacology skills, scientific reasoning, exploratory graphical analysis skills and report writing skills. Responsibilities Developing and executing modeling and simulation strategies from the early through late‑stage clinical development and serve as the SME in cross‑functional development program teams Delivering strategic and well‑timed modeling input at key decision points along the development path Set the strategy for addressing pharmacometric issues in regulatory submissions and directly influence drug development decisions Lead and drive PMX contributions to integrate relevant technical and scientific knowledge in the planning and execution of robust quantitative development programs with a focus on MIDD strategies Use state‑of‑the‑art modeling and simulation approaches to interpret PK/PD data and be accountable for ensuring appropriate PK‑PD analysis including population PK, PK‑PD modeling and simulation, and exposure‑response analysis Guide empirical modeling/QSP approaches to understand the relationship between PK, biomarkers and disease outcomes Education/Experience Requirements PhD or PharmD in Pharmaceutical sciences, Clinical Pharmacology, Mathematics, Statistics, Engineering (or equivalent) required 4+ years of relevant industry experience, including experience in NLME methods and its application in dose‑exposure‑response analysis, population PK/PD modeling, disease progression modeling and clinical trial simulation Clinical pharmacology, statistics and therapeutic knowledge in one or more disease areas Experience with incorporation of MIDD strategies into drug development across all phases and responding to questions on dose and regimen justification, study design among others Hands‑on experience with at least NONMEM and R is strongly preferred Additional Skills/Experience/Requirements The ideal candidate will embody Travere's core values: Courage, Community Spirit, Patient Focus and Teamwork Well organized with the ability to multitask, prioritize and manage shifting responsibilities in a small, fast‑moving and entrepreneurial environment Ability to manage multiple, complex tasks with competing timelines Strong interpersonal, verbal, and written communication skills Driven, intelligent, passionate about making a difference for patients with rare diseases Self‑motivated and can independently manage responsibilities 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 Ability to travel ( 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: $150,000.00 - $195,000.00 Travere Therapeutics, Inc. is an EEO/AA/Veteran/Disability Employer #J-18808-Ljbffr Travere Therapeutics
$169.22k - $253k
Job Summary Supports all pharmacometrics activities related to pre‑IND, IND, phase 1‑3, PK, PK/PD and regulatory submissions. Conducts... ..., exposure‑response and pediatric development. Author of clinical pharmacology and pharmacometrics submission documents and...SuggestedContract workTemporary workLocal areaFlexible hours$169.22k - $253k
Otsuka America Pharmaceutical Inc. is hiring a pharmacometrics expert in Washington, DC. The role involves supporting pharmacometrics activities related to drug development phases and conducting analyses for regulatory submissions. Candidates should have a PhD in pharmacometrics...Suggested$186.49k - $278.88k
...Job Summary Oversees all clinical pharmacology activities related to pre-IND, IND, phase1-3, PK, PK/PD and regulatory submissions... ...different product development team meetings. participates in pharmacometrics and simulation and modeling plans and provide input on...SuggestedContract workTemporary workLocal areaFlexible hours- ...biopharmaceutical company is seeking a qualified individual for a leadership role in pharmacometrics. This position involves developing and implementing modeling and simulation strategies across clinical programs to influence drug development decisions. The ideal candidate will...Suggested
$142.5k - $256.5k
...Associate Director, Business Analytics & Insights, Clinical Operations Reporting to the Director, Business Analytics & Operations Management, the Associate Director, Business Analytics & Insights, Clinical Operations will be accountable for development and implementation...SuggestedPermanent employmentWork at officeWork from home- Otsuka America Pharmaceutical Inc. is looking for a Clinical Pharmacology Lead in Washington, D.C. The candidate will oversee all clinical pharmacology activities and lead study design and execution. Responsibilities include conducting PK analysis and regulatory filing...Flexible hours
$90k
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...Senior Medical Director - Clinical Research About Pharming Pharming Healthcare Inc. is a global biopharmaceutical company dedicated... ...Disease Lead the napazimone pediatric study plan and clinical pharmacology studies Lead the napazimone program for new indications...Temporary workWork experience placementRemote workFlexible hours$186.49k - $278.88k
...The Director will lead activities related to Early Clinical Development (ECD) essential to the growth of Otsuka's discovery and early phase pipeline within... ...integration across discovery, nonclinical, clinical pharmacology, regulatory, and commercial functions. The...Temporary workLocal areaFlexible hours- Stryker Corporation in Bethesda, Maryland is seeking a Med-Psych Associate Medical Director to lead integrated behavioral health services. In this role, you will supervise Med-Psych and Psych APCs, provide psychiatric care, and collaborate with a multi-disciplinary team...
- ...Pennsylvania Hospitalist Associate Medical Director- Easy Access to Baltimore, D.C., and Philly Hospitalist associate medical director role: 75% clinical and 25% administrative 7 on / 7 off with flexible scheduling options Strong salary plus bonus and full benefits...Contract workRelocationRelocation packageFlexible hours
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- ...services. POSITION: Medical Director (Part Time) (15-20 hours per week)... ...Provide medical consultation to nursing and clinical staff. Perform ongoing reviews of case... ...of psychology, psychiatry and pharmacology. OTHER REQUIREMENTS : In the event...Part time
$115k - $130k
...projects. Clear communication at every level is essential—from day-to-day needs to long-term, transformative initiatives. The Associate Director of Member and Government Relations is a proactive, persistent problem solver who is the first contact for members seeking...For contractorsWork experience placementWork at officeLocal area$194k - $237k
...Associate Director, Medical Review & Training Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment approaches... ...Medical Science Liaisons on disease state landscape, clinical data, and relevant literature as needed. This individual...Full timeFlexible hours- Principal Clinical Regulatory Consultant US 3 days ago Requisition ID: 1073 Principal... ...writing, statistical analysis, clinical pharmacology, pharmacovigilance, and regulatory... ...identifying, assessing, and mitigating risks associated with clinical trials, regulatory...Work at office
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$101k - $106k
...and long-term projects along with performing day-to-day responsibilities and rapid response moments. Engagement Partner with the Director of Social Media, Health to integrate and execute education and brand-first strategies across national channels to support...Temporary work$114k - $210.9k
...Syneos Health/ inVentiv Health Commercial LLC is seeking an Associate Director of Real World Evidence to manage and design epidemiological and data science projects. The ideal candidate will have PharmaCo experience and a strong background in observational research methods...Remote workFlexible hours$91.7k - $163.7k
...advancing that mission-engaging with policymakers and shaping solutions that impact millions of people. We're looking for an Associate Director who will help drive the operational and strategic execution of our federal engagement-bringing structure, insight, and follow...Minimum wageFull timeWork experience placementWork at officeLocal areaRemote workFlexible hours$115k - $125k
...Associate Scientific Director At MJH Life Sciences our success is measured by your success! If you set your standards high and want to contribute... ...to prove it! As an Associate Scientific Director with Clinical Communications, you will be working closely with a...Temporary work$75.29k
...Closing Date: Open Until Filled Location: 4200 Connecticut Ave NW, Washington, DC 20008 Brief Description of Duties The Associate Director of Alumni Engagement, Communications, and Special Events plays a critical role in fostering lifelong relationships between...Full timeH1bWork at officeImmediate start- ...recruitment and selection of program medical directors. Participate in the training of... ...role of internal consultant to program clinical staff in the areas of hospice and... ...developed skills in: general medicine and pharmacology; Palliative medicine, pain and non-pain...Flexible hoursNight shiftWeekend workDay shiftWeekday work
$96k - $114k
29299BR Job Title: Senior IT Associate-Operations Manager-Clinical Systems (Contingent) Location: MD - Bethesda Job Description: Westat is a leader in research, data collection and analysis, technical assistance, evaluation, and communications. Our evidence...Full timeContract workTemporary workH1bWork at officeHome officeFlexible hours2 days per week3 days per week- ...them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Associate Director, Media - OBU In this role, you will support the planning, execution, and optimization of Amgen's U.S. commercial media...Flexible hours
$170.3k - $189.2k
...Earthjustice has an amazing Communications department that works in partnership with every other department at the organization. The Associate Director, Paid Media oversees the development and implementation of paid marketing strategies and multi-million-dollar media...Full timeCasual workWork at officeFlexible hoursShift work
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