Associate Director, Program Management
$195.08k - $225.22kMirum Pharmaceuticals
MISSIONMirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.POSITION SUMMARYThe Associate Director, Program Management plays a central role within Mirum by providing program management expertise and ensuring cross-functional planning and execution. The program manager partners with the Program Lead and functional leads to develop and manage the integrated product plan, develop timelines, and ensure adherence to the budget for one of our pipeline programs. JOB FUNCTIONS/RESPONSIBILITIESSupport the Program Lead with the development, communication, and timely execution of the program strategyOrganize and drive effective and action-oriented program team meetings by preparing and distributing agendas/minutes, identifying and tracking decisions and action items to resolution, and escalating areas of concern as neededPartner with the Program Lead to facilitate effective cross-functional decision making with transparent communication and clear escalation pathwaysFacilitate identification of risks which could impact the program’s strategic goals; propose and implement plans to mitigate risks or develop contingenciesDevelop and maintain integrated program timelines in conjunction with functional leadsIdentify and communicate program priorities, interdependencies, and critical path activities to all stakeholders to allow long term planning, including resource allocationOrganize the preparation of high-quality documents for review by governance committees in collaboration with the Program Lead and program teamPrepares and provides project documents and information for monthly reports, executive team updates, and board meetings.Partner with Program Lead and finance and accounting to develop annual operating plan components related to assigned program and support budget management by timely identification of out-of-scope activitiesCoordinate and manage special program-related projects, as assignedContribute to the standardization of project management best practices at MirumQUALIFICATIONSEducation /Experience:Bachelors Degree or higher in scientific/healthcare/business fieldExperience (7+ years) in clinical research and project management within the pharmaceutical industry (Biotech/small pharma experience preferred).Experience in rare disease and/or liver disease is a plus.Knowledge, Skills and Abilities:Strong ability to communicate effectively with team members creating an environment that fosters successful teamwork, collaboration and cooperation.Thorough understanding of clinical trial management processes and the operation of all clinical development functional areas.Demonstrated ability to prepare timelines and present related information to management.Proven ability to identify risks, propose mitigation strategies, and remove barriers to success.Strong attention to detail and the ability to work collaboratively with Project Lead to establish priorities for team.Expertise in developing and managing project scope, deliverables, risks and resource requirements.Strong knowledge of project management software packages and the Microsoft Office Suite: Excel, Project, PowerPoint, Word and Outlook; ability to create effective presentations for internal and external use.Ability to work in a fast paced environment with demonstrated ability to juggle multiple competing tasks and demands, across time-zones, while maintaining positive attitude.Ability to work independently, take initiative, complete tasks to deadlines and support product team in doing the same.Excellent written and oral communication skills.Displays a high level of professionalism with internal and external stakeholders.Knowledge of current regulatory requirements and guidelines governing clinical research. (e.g. ICH/GCP).The salary range for this position is $195,084 to $225,217 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.#LI-HYBRIDMirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.
$187k - $230k
...and China and capitalizing on the strengths of each geographic location.Position Summary:This role will report to the Sr. Director Program Management. This role will be the execution engine of the late-stage clinical program and manage overall project timelines, risks,...SuggestedContract workWork experience placementAfternoon shift2 days per week1 day per week$85k - $100k
...International School (INTL) is seeking a temporary Associate Director of Admission (French Program) to support the Admission Team. This is a full-time,... ...performance. The Associate Director of Admission supports the management of the enrollment process and contributes to the...SuggestedFull timeTemporary workLocal areaFlexible hoursWeekend workAfternoon shift$200k - $215k
...Ascendis Pharma is seeking an experienced Program Safety Lead to champion safety... ...roleThe role of Program Safety Lead is a director level position here at Ascendis and this... ...signal detection, evaluation, and risk management Develop and maintain safety surveillance...SuggestedFull timeTemporary workWork at officeFlexible hours$195.67k - $253.22k
...opportunity within the US Medical Affairs (USMA) organization for an Associate Director within Oncology Medical Strategy. Reporting to Executive... ...with Global Medical Affairs, Clinical Development, Alliance Management, and the broader US Medical Affairs team Provide clinical...SuggestedFull timeFor contractorsLocal areaWorldwideNight shift$186k - $233k
...Position requires 14+ years of Statistical Programming experience with exploratory-stage... ...regulatory authority audits.Timeline and vendor management for deliverables, including submission-... ...to Dose Committee meetings, Board of Director meetings, Exploratory Analysis, etc....SuggestedFull timeFor contractorsLocal area$190k - $205k
..., get it done, and have fun, seriously.POSITION SUMMARYThe Associate Director of GCP/GVP/GLP-QA is responsible for supporting Mirum’s clinical study programs as the GCP-QA representative on the study management team; managing activities involving GCP quality assurance and...Contract workLocal area$182.07k - $235.62k
...location.Reporting to the Executive Director, U.S. Prevention Public Affairs, the Associate Director of U.S. HIV Community... ...and pipeline. This includes management of long-term advocacy relationships... ...) to inform strategy, shape programs, and measure impact.Excellent communication...Full timeFor contractorsLocal area- ...possible, together.Job DescriptionThe Associate Director US Medical Affairs, Patient Access and... ...collaboration with global and USMA TA, Managed Markets, Value and Access, Commercial and... ...management of PAQ Medical Affairs Advisory Programs (MAAPs)Develop and maintain positive...Full timeFor contractorsLocal area
$190k - $220k
...Summary:Vaxcyte is seeking an accomplished Associate Director, Immunoassay Critical Reagents and... ..., governance, and lifecycle management of critical reagents and reference materials... ...customized assay materials, stability programs, and associated lifecycle management systems...Contract work$174k - $203k
...across communications and decision making.Summary:The Associate Director, Process Validation and Risk Management will lead and facilitate commercial process... ...PPQ, CPV, lifecycle validation) across commercial programs.Lead and facilitate execution of validation strategies...$195.67k - $253.22k
...patients for generations to come. As Associate Director, Generative AI, at Gilead you will report... ...model evolution of external solutions. Manage and work with IT on choice of platform... ...Demonstrated ability to deliver complex programs with measurable impact. Proven ability...Full timeFor contractorsLocal area$174k - $203k
...communications and decision making.Summary:The Associate Director for Drug Substance (DS)... ...appropriate planning for commercial lifecycle management. This position will be reporting into... ...Director will collaborate on overall program strategy, with primary responsibility...Remote work$158.2k - $197.8k
As the Associate Laboratory Director, Oncology and one of our Laboratory Directors, you have clinical oversight... ...-approved proficiency testing (PT) program for the test performed; PT samples... ...manual is available to all personnel.Manage a team: review and approve assigned...Immediate startWorldwide$180k - $210.5k
...and filing of regulatory CMC submissions. Manages interactions with Health Authorities for... ...deadlines across a variety of projects/programs, with a high degree of accuracy and... ...and ICH) guidelinesReports to: Executive Director, CMC RegulatoryLocation: San Carlos, CA...$170k - $198k
...individual to join Vaxcyte's Global Analytical organization as Associate Director, CMC Statistician. The position will be an integral part of... ...development, PPQ, BLA readiness, and commercial lifecycle management. This individual will collaborate with Process Development,...Remote work- ...generations to come.We are looking for an Associate Director, Clinical Pharmacology based in our... ...disease or therapeutic area.Leads and manages design and conduct of clinical pharmacology... ....Experience using pharmacokinetic program and analysis software (such as WinNonlin...Full timeFor contractorsWork at officeLocal areaFlexible hours
$200k - $230k
...PharmaceuticalsPosted: 2026-08-04Associate Director, Medical Communications (VLX... ....Position SummaryThe Associate Director/Director, Medical... ..., and engaging tools and programs that support Mirum... ...will also collaborate in the management of the database of Medical Field...Local area$182.07k - $235.62k
...improving the lives of patients for generations to come. The Associate Director, Quality Assurance - GMP Operations provides senior Quality... ...improvement statistical.Demonstrates working knowledge of Risk Management tools (e.g., Hazard Analysis and Critical Control Points (...Full timeContract workFor contractorsLocal area$155k - $190k
...Job Title: Associate Director, Clinical Data Systems and Informatics Location: San Mateo, CA;... ...development of our diagnostic tests through management of clinical data flow into our data... ...forms (eCRFs), including edit check programming and UAT execution Manage data flow from...$170k - $200k
...Job Description Description Codexis, a biotechnology company based in Redwood City, CA, is looking to hire an Associate Director of Program Management . Codexis is a leading enzyme engineering company leveraging its proprietary CodeEvolver® technology platform to...Temporary workSummer holidayFlexible hours$155.8k - $194.7k
...Overview The Associate Director, Laboratory Operations is a key leader in Natera’s lab operations who oversees and... ...recommends manufacturing policies, procedures and programs. Selects, develops and evaluates line-management to ensure the efficient operation of the...Contract workFor contractorsWork at officeImmediate start$219k - $256k
...Director, Global Drug Substance Commercialization, Critical Raw Materials Join to apply... ...raw materials for production of eCRM and associated components for glycoconjugate vaccines.... ...network, including materials management and data analytics. Process validation...RelocationRelocation package$120.2k - $223.2k
...into the Head of GPAL in the Global Legal Pharma Department.Associate Program Directors of Commercial Medical Legal Regulatory Review Committees (... ...with oversight from CORA Program Directors and their managers. They are experienced individual contributors expected to...Full timeWork experience placementLocal areaWorldwideRelocation package$190k - $205k
..., ensuring compliance with applicable regulatory requirements. Manages the development, implementation, and continuous improvement of... ...inspections and thorough understanding of audit and vendor management programs.Excellent organizational skills: Proactive, management of...Local area$195.67k - $253.22k
...confronting the largest public health challenges of our day and improving the lives of patients for generations to come.As an Associate Director, Data Management, MDM Governance & AI Enablement at Gilead, you will join the US Commercial Data Strategy and Governance team in a...Full timeFor contractorsLocal area$195.67k - $253.22k
...aspirations. Join Kite and help create more tomorrows. As an Associate Director, CAR-T Payer & Value Marketing, at Gilead you will lead the strategy... ...partners where applicable to ensure unified execution5) Manage External Partners & Execution ExcellenceLead agency of record...Full timeFor contractorsLocal area$190k - $220k
...Summary:Vaxcyte is seeking an accomplished Associate Director, Immunoassay Development to join the... ...transfer, validation, lifecycle management, routine analytical testing, and immunoassay... ...for complex conjugated vaccine programs and other vaccine pipeline assets.The...Contract work- ...together.Job DescriptionAssociate Director, Global Supplier QualityPosition SummaryThe Associate Director, Global Supplier Quality serves as the global program owner providing leadership for... ...compliant Approved Supplier List management.Robust supplier master data integrity...Full timeContract workFor contractorsLocal area
$195.67k - $253.22k
...Associate Director, Patient Safety-Virology At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled... ...across functions to support product development, lifecycle management, and post‑authorization safety activities. Key...$160k - $225k
..., air quality sensors, alarms, intercoms, and visitor management. We’ve got serious momentum in the market: more than 3... ...countries. About the RoleWe are looking for a driven Associate Solutions Engineering Program Manager to lead and mentor a team of Associate Solutions...Full timeWork at officeWork visaFlexible hoursShift work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Associate Director, Program Management. Be the first to apply!
- associate director Foster, CA
- associate scientific director Foster, CA
- associate manager Foster, CA
- remote associate product manager Foster, CA
- localization program manager Foster, CA
- senior director program management Foster, CA
- program manager government Foster, CA
- staff program manager Foster, CA
- program manager full time Foster, CA
- nutrition program coordinator Foster, CA

