Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
Position: The Senior Director of Clinical Pharmacology (CP) will oversee CP efforts across clinical development. As an early member of the CP function, you will have an opportunity to influence the direction of the CP function at Nurix. As a CP lead, you will provide subject matter expertise and program-level functional and operational leadership to the clinical development team(s) on all issues related to CP. You will develop and manage CP strategies including quantitative pharmacology plans and model-informed drug development strategies as appropriate (population analyses, exposure-response, PBPK, QSP, etc).The successful applicant is proficient in the use of innovative methods to integrate knowledge of PK and PD to optimize posology for early and late-stage clinical trials while collaborating with clinicians, clinical operations, bioanalytical, biomarker, pharmacovigilance, regulatory, and CMC groups. In addition, this individual will work closely with the project team to create clinical development plans that include assessments of a drug's efficacy, safety, commercial viability and fulfillment of registration requirements. This role requires strong communication and interpersonal skills and involves leading a team of scientists to develop and manage CP strategy for compounds from pre-clinical to post-marketing approval.
Please Note: This role requires 2-3 days on site in our San Francisco office. Relocation assistance may be available.
ResponsibilitiesDevelop CP development plans, timelines and prioritization of studiesOversee and contribute to CP sections of clinical study protocols, SAPs, CSRs, stand-alone PK/PD reports, Clinical development plans, Regulatory documentsMultidisciplinary collaborations to ensure modelling and simulation methods (e.g., QSP, MIDD, PBPK) inform internal decision making and external regulatory relationsFoster cross functional (Clinical operations, Research, Bioanalysis, Biometrics, CMC, Regulatory, and Clinical Sciences) collaborations to guarantee seamless implementation of Phase I-III studiesCapable of integrating PK, PD, and safety data from multiple sources to optimize dosing for patient populations across the development continuumOffer input on preclinical-stage programs to augment preclinical effectiveness and biomarker data to support the progression of programs into clinical development
QualificationsPhD/PharmD degree in a field related to Pharmacokinetics with at least 12+ years of industry or similar experience in CP or Quantitative Systems PharmacologyDemonstrated exemplary PK/PD experience in managing clinical and nonclinical projects; and interactions with global regulatory agencies for NDAProven record of implementing MIDD approaches (e.g., BE, DDI, biowaivers)Current knowledge of regulatory guidance, global regulations, and SOPs in the conduct of clinical pharmacology studiesExceptional oral and written communication skills and excellent problem-solving skillsDemonstrated past performance of functioning efficiently in a dynamic, cooperative, team-oriented environment showcasing emotional intelligence (respect and empathy)High proficiency in using common software and data analysis packages (e.g., WinNonlin, Simcyp, GastroPlus, GraphPad Prism, Microsoft Office, PowerPoint, Excel, Word)Nurix Therapeutics, Inc. is committed to protecting and respecting your privacy and personal information, including information collected by Nurix when you apply for a job with Nurix or in the course of your employment with Nurix. By applying for a position at Nurix, you agree to our collection and use of personal information as described in our Privacy Policy ( ).
Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
PositionNurix has a place for an extraordinary, highly motivated, self-starter and accomplished Associate Director of Clinical Data Management to become a part of the growing biometrics organization.
SummaryThe Associate Director of Clinical Data Management (CDM) will be responsible for the delivery and integrity of clinical data across Nurix's multiple studies/programs. The role will also be supporting process development and improvement in building clinical data management infrastructure. He/She will ensure adherence to industry guidelines in all clinical data management activities for assigned studies, as well as assisting in the development and implementation of departmental policies, operational guidelines, and administrative structure. The successful candidate should have a successful track record in managing vendors and effectively leading study clinical data management activities with the anticipated growth in the product pipeline. He/She must also possess excellent communication skills work closely with medical study directors and clinical operations to provide and receive direction to ensure high quality and integrity in clinical data.Additional key representative responsibilities will include, but not necessarily be limited to, the following:
Job Responsibilities:Lead and manage clinical data management duties and tasks for assigned clinical trial from study start up to study closeoutManage and provide oversight of vendors (including clinical data management CRO) that have been contracted to handle Nurix's clinical data and ensure the data are complete, accurate and delivered within the agreed upon timelinesEnsure inspection readiness by maintaining current documentation, adherence to industry guidelines, SOPs and compliance with trainingWork collaboratively with internal and external team members within the study to coordinate the planning and execution of clinical data management activitiesCreate strategies for rapid study start and database lock to increase clinical data management productivityLead the design of the eCRFs and ensure that they align with the clinical protocol(s)Ensure complete and accurate documentation such as eCRF specifications, eCRF completion guidelines, annotated CRFs, data validation specifications, data transfer agreements, and data management plansEnsure data is reviewed on an on-going basis, including individual subject data within the EDC, datasets, TLFs, etc. that are generated for CSRs, DSURs, IBs, and other business needsCollaborate with clinical development team and provide expertise regarding CDISC data standards, FDA and ICH guidelines, and GCDMP standardsHelp establishing CDM processes and contribute to the development of key clinical data management SOPsProvide technical support and guidance for clinical data management team and vendors around project conventions, standards, practices, and database specificationsPerform budget review and guidance for clinical data management CRO for assigned trial
QualificationsBachelor's degree in a scientific discipline or equivalent (computer science, mathematics, statistics, epidemiology, biology, psychology). A Master's degree in a related science field is preferredMinimum of 10 years of clinical data management experience within pharmaceutical industry with a track record of success and progression for Associate Director levelMinimum of 12 years of clinical data management experience within pharmaceutical industry with a track record of success and progression for Director levelDirect experience working with Medidata Rave design and implementationProficient on regulatory requirements for clinical data management and the regulatory submission processExtensive experience working with external vendors, including but not limited to acquisition, contracting, evaluation of vendor's capabilities and ensuring the desired high-quality deliverablesDemonstrated ability to operate and lead assigned study in a dynamic organization, build successful working relationships and effective stakeholder management in an environment that requires diverse educational and functional expertiseAble to adapt quickly to the changing needs of the organizationAble to organize multiple work assignments and establish prioritiesExcellent verbal and written communications skills; able to communicate proactively and effectivelyNurix Therapeutics, Inc. is committed to protecting and respecting your privacy and personal information, including information collected by Nurix when you apply for a job with Nurix or in the course of your employment with Nurix. By applying for a position at Nurix, you agree to our collection and use of personal information as described in our Privacy Policy ( ).
Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
Position The Executive Director Global Value and Market Access will be responsible for developing and executing differentiated global market access and pricing strategies demonstrating the value of our assets to HTA bodies and payers to ensure optimal patient access. The ideal candidate will have a solid analytical background, strategic thinking as well as a deep understanding of US / EU /Japan/ Canada regional healthcare systems, payer preferences, and market dynamics to lead the market access and pricing launch strategies.
Responsibilities
Lead the development of Global Integrated Access and Pricing strategies in collaboration with the cross-functional team to maximize the value of assigned asset(s),Provide strategic market access input to inform global clinical development program of assigned asset(s) and ensure it is optimized to meet the needs of global payers (e.g., relevant endpoints, trial design, sub-populations, evidence of cost offsets) by incorporating HTA and payers' perspectives gained through early HTA engagement, ad boards, primary payer research, and analysis of select secondary research,Develop and maintain strong business relationships with key functions responsible for value proposition enablement with a focus on clinical, commercial, regulatory, medical affairs, and HEOR stakeholders,Proactively identify and communicate evidence requirements for successful access and support the development of evidence generation plans in collaboration with HEOR,Collaborate with Market Access colleagues (Global and in countries) to drive alignment, optimize support, and promote efficiency and best practice sharing,Monitor, analyze and communicate Global market access and pricing trends, competitor activities, and policy changes to anticipate future market dynamics and adjust strategies accordingly,Support the execution of broader market access goals, including pricing targets, access timelines, and overall launch success,Plan and contribute to JCA submission.
Requirements
Ph. D, Pham D, M. Sc. in appropriate field (Health Economics, Public Health, or Health Policy) preferred. years of relevant experience working within a similar organization including international exposure within a leadership position,Strong experience in pricing and reimbursement of hematology / oncology products with specific knowledge of and demonstrated experience in one of the key HTA markets (i.e., UK, Germany, France, Canada),Strong experience with pricing regulations and a hands-on role in early and launch Pricing analysis. Hands-on experience with country pricing negotiations is a plus,Demonstrable experience supporting the early global development plans to meet the evidence requirements for the various downstream market access stakeholders,Proven track record of success within developing desirable value propositions and access strategies,Demonstrated knowledge of global policy trends, tactics, and HTA/payer dynamics incl. regional developments (e.g., JCA, IRA),Experience in making market access recommendations on products in development and suggesting changes for optimization of market access,Demonstrated success in managing multiple activities (both "self" and through delegation) and working in a fast-paced environment,Proven track record of providing thought leadership, influencing decisions across all levels of the organization, and driving results through teams,Fluency in English and an additional language would be a strong advantage.
Fit with Nurix Culture and ValuesStrong team orientation; highly collaborativeSolutions and results-oriented focusHands-on approach; resourceful and open to diverse points of view
Application ProcessNurix is an Equal Opportunity Employer offering a competitive salary and benefits package. Applicants should be legally entitled to work for any employer in the US.Nurix Therapeutics, Inc. is committed to protecting and respecting your privacy and personal information, including information collected by Nurix when you apply for a job with Nurix or in the course of your employment with Nurix. By applying for a position at Nurix, you agree to our collection and use of personal information as described in our Privacy Policy ( ).
Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
Position The Sr Director Business Insights & Analytics is responsible for market research, competitive intelligence, and forecasting for the Hematology assets of Nurix Therapeutics, and other assets and therapeutic areas as assigned.
The successful candidate will focus on critical business questions, drives towards strategic and synthesized insights, and suggests ideas and recommendations that enable better decision-making for the business.
This role will utilize advanced analytics to inform critical decisions for R&D, Business Development, New Product Planning, and the Commercial organization broadly. The ideal candidate for this role is a strategic, forward-thinking, analytics professional with a passion for fostering change and driving long-term sustained growth for the company.
Duties and Responsibilities:
Drive robust delivery related to: Primary Market Research, Forecasting, Competitive IntelligenceLead and drive a thought partnership with brand teams and cross-functional partners to understand and address key business questions.In partnership with Brand Marketing, Sales Leadership, Finance, Patient Support, Market Access and other stakeholders, this role provides leadership in developing and executing the commercial strategy and plan by providing meaningful market and brand insights that enable effective data driven decision-making.Translates the business needs into actionable analytic-focused initiatives to provide solutions and/or recommendations to enable business excellence.Provide analytical insights through data analytics and market research to the Commercial teams to understand the business and identify potential opportunities for future growth.Lead sales forecasting and planning processes used within the Commercial organization and provide assessments of all business development opportunities to determine viability.Liaison between the Commercial organization and supply chain team to plan on optimal production and stocking of commercial product.Maintains a thorough understanding of the competitive landscape, market environment and product development to provide data-driven recommendations and consultation to Executive/Senior level leaders.Responsible for financial management of the function, including budgets, resources and ensuring productivity against impact is delivered.
Education and Qualifications
B.S. degree, advanced degree preferred.Experience launching products in biopharma industry (preferred).Hematology / Oncology experience (preferred).Strong command of analytical and market research techniques and experience with selection and management of vendors.Experience building and maintaining complex market assessments and forecast models.Ability to create and communicate a clear vision among direct reports, effectively aligning resources and motivating teams to achieve goals.A proven record of leading and delivering strategic initiatives for commercial executive leadership teams with tangible results using advanced analytics expertise.High business acumen with demonstrated ability to distill complex problems, create structured framing, assessments, and actionable recommendations in collaboration with cross-function/division colleagues.
Fit with Nurix Culture and ValuesStrong team orientation; highly collaborativeSolutions and results-oriented focusHands-on approach; resourceful and open to diverse points of view
Application ProcessNurix is an Equal Opportunity Employer offering a competitive salary and benefits package. Applicants should be legally entitled to work for any employer in the US.
Nurix Therapeutics, Inc. is committed to protecting and respecting your privacy and personal information, including information collected by Nurix when you apply for a job with Nurix or in the course of your employment with Nurix. By applying for a position at Nurix, you agree to our collection and use of personal information as described in our Privacy Policy ( ).
Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
PositionWe are seeking a talented scientist with a strong background in Biophysics to join our Drug Discovery Technology Department. In this laboratory-based position (one year contract with an opportunity to renew), you will be part of a diverse team that is focused on advancing projects by collecting and interpreting biophysical assay data for ongoing discovery programs, hit identification, and hit to lead efforts. You also will be responsible for implementing novel biophysical assays and techniques to expand our capabilities. You will work closely with an experienced team of interdisciplinary scientists and have regular opportunities to present findings to project teams and senior management. The successful candidate will have the opportunity to directly contribute in the following areas:Plan and execute small molecule-protein biophysical assays to characterize binding affinity and kineticsIdentify novel chemical matter using biophysical screening techniques of extensive small molecule compound librariesCharacterize the binding affinity and kinetics of binary and tertiary complexes of proteins and targeted protein degrader moleculesCharacterize the binding of small molecule-DNA conjugate molecules from DNA-encoded library (DEL) screening campaignsEvaluate new technologies and develop novel biophysical assaysEngage in cross-functional team discussions that support our DEL screening groups, internal project teams, collaboration projects, and machine learning effortsPrepare reports and present data at internal group meetings
Education and ExperiencePh.D. in Biophysics, Biochemistry, or related discipline 0 years relevant experience OR MS with 3 years relevant experience, OR BS or equivalent with 5 years relevant experienceExperience using biophysical techniques to analyze protein-small molecule interactionsExtensive, hands-on laboratory experience in the use of Surface Plasmon Resonance biosensors (SPR) or Grating-Coupled Interferometers (GCI)Expertise in the kinetic and thermodynamic characterization of ligand binding as well as quantitative data management and analysisPractical experience with biophysical techniques such as Microscale Thermophoresis (MST), Isothermal Titration Calorimetry (ITC), Differential Scanning Fluorimetry (DSF), and Nuclear Magnetic Resonance (NMR) is preferredExcellent communication skills and ability to present scientific rationale, key data, issues and accomplishments to other scientific colleagues
Added QuantificationsExperience working in PROTAC-based drug discovery programsExperience working with molecular biology tools (PCR, qPCR, Western Blot)Experience with medicinal chemistryGood fit with Nurix cultureThe ideal candidate must be able to commit to 1year in this role.Nurix Therapeutics, Inc. is committed to protecting and respecting your privacy and personal information, including information collected by Nurix when you apply for a job with Nurix or in the course of your employment with Nurix. By applying for a position at Nurix, you agree to our collection and use of personal information as described in our Privacy Policy ( ).
Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
Position Overview: The High-Throughput Synthesis Scientist will design and execute automated parallel synthesis experiments. This role involves collaborating with Medicinal Chemists and DEL scientists to optimize and validate chemical routes for transfer to parallel synthesis platforms using both solution phase and solid phase chemistry approaches. The scientist will also contribute to the design, development, optimization, validation, and integration of complex automation systems for high-throughput automated synthesis. An active presence in the laboratory and a 'can-do' attitude are essential.
Key Responsibilities: Design and synthesize chemical arrays using automated synthesis platforms. Develop new methodologies for solid phase parallel automated synthesis. Participate in daily operations and maintenance of various automated equipment. Collaborate with medicinal chemistry teams and DEL scientists to leverage automated chemistry capabilities for advancing discovery programs. Contribute to scientific strategies and goals within a project team setting.
Requirements: Doctorate degree with 2 years of medicinal chemistry or pharmaceutical research experience, OR Master's degree with 5 years of medicinal chemistry or pharmaceutical research experience, OR Bachelor's degree with 7 years of medicinal chemistry or pharmaceutical research experience.
Required Skills and Experience: Expertise in applying parallel synthesis techniques to synthetic and medicinal chemistry. Ability to work in a cross-functional environment with a proactive mindset to enhance productivity and efficiency. Proficiency in operating, maintaining, and troubleshooting high-throughput synthesis systems. Excellent organizational and communication skills, coupled with strong analytical and problem-solving abilities. Working knowledge of solid phase synthesis and solution phase synthesis with solid supported reagents.
Preferred Skills and Experience: Proficiency in utilizing automation systems for high-throughput applications within pharmaceutical, biotech, or related industries. Experience with operating and programming liquid handling robotics platforms. Familiarity with modern cheminformatics tools, computational tools, enumeration tools, and other scientific software for drug discovery. Practical knowledge of medicinal chemistry principles.
Nurix Therapeutics, Inc. is committed to protecting and respecting your privacy and personal information, including information collected by Nurix when you apply for a job with Nurix or in the course of your employment with Nurix. By applying for a position at Nurix, you agree to our collection and use of personal information as described in our Privacy Policy ( ).
Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
Position Design and management of safety pharmacology, exploratory and GLP toxicology studies. Handle multiple projects in a timely and effective manner at various stages of discovery, preclinical and clinical development. Write, interact, and/or contribute to all applicable Regulatory Documents/Authorities and Asset Teams.
Responsibilities Lead toxicology strategy and tactics in discovery, preclinical development and clinical development with a focus on understanding/assessing the human risk of novel therapeutic targets and/or understanding mode of action for toxicity in nonclinical studiesParticipate in multi-disciplinary team efforts and implement program-specific toxicology strategies to support compound and program progressionServe as the internal study directory and primary point-of-contact with CRO partners, interacting with technical, veterinary, and scientific staffMonitor outsourced GLP and non-GLP studies ensuring compliance with the protocol, amendments, regulations, safety guidelines, and standard operating proceduresWrite and review toxicology reports and documentation for regulatory filings, and participate in regulatory interactionsApply a broad understanding of toxicology, pharmacology, ADME, and knowledge of applicable regulatory guidelines to the design of appropriate toxicology studies and development plansProvide creative approaches to expedite nonclinical development strategiesProvide a critical review of toxicology study protocols, data and study reportsServe as the Toxicology representative on multi-functional project teams supporting discovery and development phase projectsContribute to the preparation of high-quality regulatory documents supporting global clinical development and marketing authorizationsEffectively communicate toxicology study results to project teams and senior level managementTravel required as needed.
Required Qualifications Ph.D. in Toxicology, Pharmacology, or a related field with a minimum of 5 years of industry experience as part of a drug development project team or a minimum of 5 years FDA experience reviewing nonclinical regulatory submissionsSubstantial nonclinical development experience at a pharmaceutical or biotechnology company or with the FDAExperience in designing, monitoring and interpreting nonclinical toxicology/safety pharmacology studiesExperience in writing and reviewing nonclinical sections of regulatory documents (CTA, IND, IB, NDA, BLA, etc.) and direct interactions with worldwide regulatory agencies
Bonus QualificationsCertification by the American Board of Toxicology (DABT) is highly desiredNurix Therapeutics, Inc. is committed to protecting and respecting your privacy and personal information, including information collected by Nurix when you apply for a job with Nurix or in the course of your employment with Nurix. By applying for a position at Nurix, you agree to our collection and use of personal information as described in our Privacy Policy ( ).
Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
Position The Executive Director of Hematology Marketing will work cross-functionally and serve as an instrumental leader to enable the successful development and commercialization of Nurix Therapeutics Hematology assets.How you will contribute• Establish strategic direction of pre-launch, launch and commercialization of Nurix assets in hematology.
• Drive Strategy and Launch Tactical Planning activities for key assets across multiple indications.
• Partner to shape the Heme Disease Area Strategy, Brand Strategy and Brand Plan, including financial plan and forecasts, life cycle management
SCOPE :• Support the development of the strategic direction of Heme portfolio; validate growth opportunities and prioritize key activities
• Drive the Global and US strategy and launch plans in Heme.
• Drive insight generation and translate insights to messaging and brand storytelling in collaboration with Analytics and Insights; apply data and insights to validate business opportunities, optimize marketing mix and monitor ROI of brand activities
• Lead the development and execution of tactical mix to drive brand performance.
• Support LCM strategy for key assets by evaluating and prioritizing value driving indications.
Required Qualifications• Bachelors Degree
• At least 10 years pharmaceutical experience with increasing responsibilities in sales or marketing, including launching brands in the US market
• At least 3-5 years of leadership experience - hired, developed and managed talent within the industry
• Deep understanding of the pharmaceutical industry, with experience in either Hematology / Oncology
• Deep understanding of the brand/franchise, the pharmaceutical industry and how to effectively engage HCPs
• Demonstrated ability to collaborate with functional partners and peers
• Demonstrated experience managing complexity and change
• Learning agility and adaptability
• Ability to set priorities, manage roles and responsibilities of team, mentor and develop team members
• Ability to make sound business decisions based on a strong understanding of business, finance and risks/benefits of decisions
• Extensive experience in marketing strategy and tactic design with an ability to communicate ideas to internal partners and external agencies
• Ability to clearly and succinctly communicate (verbally/written) in a persuasive and appropriate manner at the executive level
Fit with Nurix Culture and Values
• Strong team orientation; highly collaborative
• Solutions and results-oriented focus
• Hands-on approach; resourceful and open to diverse points of view
Application ProcessNurix is an Equal Opportunity Employer offering a competitive salary and benefits package. Applicants should be legally entitled to work for any employer in the US.Nurix Therapeutics, Inc. is committed to protecting and respecting your privacy and personal information, including information collected by Nurix when you apply for a job with Nurix or in the course of your employment with Nurix. By applying for a position at Nurix, you agree to our collection and use of personal information as described in our Privacy Policy ( ).
Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
Position We are seeking a dynamic and experienced Vice President of Marketing with extensive experience launching new hematology / oncology products and incorporating commercial strategy into early development programs. The core objective is to build, lead and execute all aspects of Nurix Therapeutics marketing efforts. This individual will be responsible for developing all marketing strategies and tactical readiness for the commercialization of Nurix Therapeutics assets. In addition, this role will be accountable for driving commercial strategy in support of lifecycle management and our pipeline. Accountable for developing and executing all Global and US Marketing strategies that align with the overall company strategic imperatives.
Ensure strategic alignment with cross-functional commercial partners in commercial insights and analytics, market access, and sales in order to produce high quality marketing efforts that achieve company performance objectives
• Build and implement the marketing plan including, but not limited to, marketing strategy, brand development, promotions, digital marketing, patient marketing, and marketing operations
• Develop and execute a comprehensive commercial strategy and set of tactical plans to ensure successful commercial launch of Nurix's lead asset and subsequent assets in the US and other ex-US markets
• Partner with commercial insights and analytics to develop and maintain deep market insights through market research, competitive intelligence, business analytics, necessary metrics/KPIs are in place to measure performance and identify opportunities as needed
• Lead the development and implementation of commercial plans for potential future products including situation analysis, sizing/segmentation, positioning, messaging, and go-to-market commercial strategies
• Partner with Clinical Development to inform trial design and prioritization of lifecycle plans and future pipeline assets
• Maintain a high degree of presence, visibility, and ensure regular and effective communication with the field sales team to regularly solicit input, feedback, ideas, identify challenges and opportunities to deliver solutions as needed
• Partner with commercial insights and analytics and finance to develop and maintain commercial forecasts, quarterly latest estimates, and operating budgets
• Proactively develop and maintain close relationships with US and international Thought Leaders to inform commercial strategy
• Ensure successfully agency and vendor partnerships
• Participate in portfolio strategy and commercial evaluation of business development opportunities as needed
• Provide input as needed to other business planning processes such as IC planning, CMC, budgeting, etc
• Ability to travel (domestic and some international) to attend industry and team/field sales meetings, customer engagements, market research
Requirements:• Bachelors degree in business or related discipline required; MBA strongly preferred
• Minimum of 15 years of experience within the biotech/pharmaceutical industry
• U.S. Hematology/Oncology launch experience is required; Global launch experience strongly preferred
• Experience building teams and commercial capabilities is required
• Demonstrated ability to deliver results in competitive markets
• Proven success collaborating closely with other commercial disciplines (market access, sales, operations, training, insights/analytics, etc)
• Must be highly analytical, and comfortable with formulating and delivering data-driven, fact-based analysis of the business and utilizing insights to propose effective marketing strategies
• Must be resourceful, demonstrate an agile and lean mindset approach, creative problem solver who seeks out and is receptive to new ideas and approaches to solving challenges
• Ability to adapt to changes in the work environment, industry, manages competing demands
• Outstanding written and verbal communication skills with the ability to effectively present to and engage with a wide range of audiences
• Strategic thinking with the ability to drive results in a fast-paced and dynamic environment
Fit with Nurix Culture and ValuesStrong team orientation; highly collaborativeSolutions and results-oriented focusHands-on approach; resourceful and open to diverse points of viewNurix is an Equal Opportunity Employer offering a competitive salary and benefits package. Applicants should be legally entitled to work for any employer in the US.Nurix Therapeutics, Inc. is committed to protecting and respecting your privacy and personal information, including information collected by Nurix when you apply for a job with Nurix or in the course of your employment with Nurix. By applying for a position at Nurix, you agree to our collection and use of personal information as described in our Privacy Policy ( ).
