Director, Molecular Diagnostics Program at Ultragenyx in Novato, CA

Why Join Us? Be a hero for our rare disease patients At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to do. To achieve this goal, our vision is to lead the future of rare disease medicine. For us, this means going where other biopharma companies won’t go – challenging the status quo and creating a new model that advances our field so more patients and caregivers can benefit from life-changing treatments. We do this by following the science, applying a novel rapid development approach, making innovative medicines at fair and reasonable prices, and creating a collaborative ecosystem to reach patients in ways that are most meaningful for them. Our commitment and care for patients extends to our people, so culture is an essential cornerstone for Ultragenyx. We remain continuously focused on creating a supportive and inclusive environment of profound learning and growth – so employees can thrive in all areas of their lives, in and outside of work. Ultimately, we want to be an organization where we would be proud for our family, friends and children to work. If you want to have a meaningful impact, do the best work of your career, and grow a lot, both professionally and personally, come join our team.

Position Summary:

ultraimpact – Make a difference for those who need it most

The Molecular Diagnostics Programs - Director will develop and manage diagnostic programs in support of timely and accurate diagnosis of rare disease patients. This is key role in Global Medical Affairs that contributes to the strategic vision and objectives of the team. The Director, Molecular Diagnostics Programs requires the integration of technical, genetic, and diagnostic expertise with program data to recognize and communicate program and scientific insights. The Director collaborates internally with Medical Affairs, Publications, Bioinformatics, Commercial, Regulatory, Legal, and other business functions for program execution. Successful candidates have a history of effective collaboration with cross functional teams in a matrix environment, engagement with external stakeholders and clinicians regarding diagnostic testing, experience with molecular, biochemical, or diagnostic commercial test development.

Work Model:

Remote: Officially documented as working full-time from home, with travel to Ultragenyx's offices or other locations on occasion as needed.

Responsibilities:

Provide Molecular Diagnostics Programs testing solutions for franchise and pipeline programs and patients.
Drive for clarity on testing program requirements and anticipate the needs of medical and commercial teams, drawing on expertise in diagnostic, molecular, and/or biochemical laboratory testing
Support global operational planning and execution for clinical laboratory testing programs based on experience testing program launches and by partnering with internal and external scientific, laboratory, and clinical director experts to inform patient diagnosis needs and program success
Lead cross-functional marketed-product stage diagnostic testing program workstreams for one or more program and in two or more geographies
Monitor and report on molecular diagnostics program status to the business
Develop internally and/or externally facing laboratory testing program-associated materials, maintain medical and compliance review of such materials
Support development and maintenance of gene locus-specific databases in partnership with internal teams and external submitters
Analyze sponsored diagnostic program data, develop program summaries, and suggest program insights for internal and external publication and scientific exchange
Provide subject matter expertise through training on molecular diagnostics programs as well as reviews of relevant program materials
Uses diagnostic acumen and understanding of Ultragenyx priorities to identify strategic needs in rare disease diagnosis among commercial clinical laboratory offerings, working seamlessly with internal & external partners to co-develop and implement program-specific solutions

Requirements:

Master’s or PhD in: genetics, biochemistry, genetic counseling, molecular biology or related field and >10 years industry experience
Experienced in commercial genetic, biochemical, and/or other diagnostic assay development and testing program operational execution
Demonstrated ability to successfully manage competing priorities & deliverables in a fast-paced, dead-line oriented environment
Superior organizational, problem solving, and analytical skills
Able to build strong cross-functional relationships
Strong oral and written communication skills and excellent presentation skills
Understanding of cloud platform, enterprise software and services, API integration, databases, mobile and consumer applications, device integration, or user experience preferred
Preferred skills include experience with data visualization software, PowerBI or Tableau, familiarity with HGVS nomenclature, molecular/biochemical/antibody testing, disease-databasing, or experience in health informatics, computer science, information systems or related field #LI-Remote #LI-DNI

The typical annual salary range for this full-time position is listed below. This range reflects the characteristics of the job, such as required skills and qualifications and is based on the office location noted in this job posting. The range may also be adjusted based on applicant's geographic location.

This position is eligible for annual bonus and equity incentives. Actual individual pay is determined by demonstrated experience and internal equity alignment.

Pay Range$210,400—$259,900 USD Full Time employees across the globe enjoy a range of benefits, including, but not limited to: · Generous vacation time and public holidays observed by the company · Volunteer days · Long term incentive and Employee stock purchase plans or equivalent offerings · Employee wellbeing benefits · Fitness reimbursement · Tuition sponsoring · Professional development plans * Benefits vary by region and country

Ultragenyx Pharmaceutical is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital and veteran status, and any other status or classification protected by applicable federal, state, and/or local laws. Reasonable accommodation will be provided for all protected statuses or classifications protected by applicable law, including individuals with disabilities, disabled veterans, for pregnancy, childbirth, and related medical conditions, and based on sincerely held religious beliefs. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or in any part of the recruitment process, you may contact Talent Acquisition by emailing us at talentacquisition@ultragenyx.com.

See our CCPA Employee and Applicant Privacy Notice. See our Privacy Policy.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Note to External Recruiters: All candidate activity and open positions are managed strictly through our Human Resources Department. Our Human Resources Department kindly requests that recruiters not contact employees/hiring managers directly in an attempt to solicit business and present candidates. Please note that failure to comply with this request will be a factor in determining a professional relationship with our organization. Submission of unsolicited resumes prior to an agreement set in place between the Human Resources Department and the recruiting agency will not create any implied obligation. Inquiries on developing a recruiting relationship with us, may be directed to: talentacquisition@ultragenyx.com.