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ADAPTED_NOW

Clinical Director

Advanced degree in clinical or biological sciences (MD, PhD, or PharmD preferred) and 4+ year's (Associate Dir) or 8+ years (Director) relevant drug development experience with minimum of 3 years’ experience in oncology clinical trials. This role will work cross-functionally and participate in the execution of clinical studies including protocols, provide scientific expertise to support site and CRA training, data cleaning/analysis, investigator interaction and support of regulatory filings.

KBSkills

ACTIVE

Job Summary:As an integral member of the Clinical Development Team, this person will work closely in collaboration with the study teams providing scientific guidance and support.The Associate Director/Director, Clinical Science will report to the VP, Head of Clinical Science or a more senior member of the Clinical Science team. They will be responsible for contributing to the strategy to advance molecules through the Nurix clinical pipeline. This role will work cross-functionally and participate in the execution of clinical studies including protocols, provide scientific expertise to support site and CRA training, data cleaning/analysis, investigator interaction and support of regulatory filings. In collaboration with the Medical Monitor and Safety team this role will be responsible for safety oversight of clinical trials. Responsibilities:<ul><li>Participate, contribute to cross-functional clinical development teams with strong ability to work closely with all team members, address study or other program-specific questions.</li><li>Implement Global Development Plan with strategic clinical science support.</li><li>Authoring and/or reviewing clinical protocols.  Read and interpret scientific and medical literature for the use in clinical documents and to assist clinical team decision making.</li><li>Prepare clinical portions of all relevant regulatory filings and meeting packages (INDs, Annual Reports, meeting requests, NDAs, etc.) for US and ex-US Health Authorities as needed.</li><li>Integrate scientific knowledge and operational expertise to ensure translation of clinical research plans into efficiently delivered high quality studies.</li><li>Acquire and utilize knowledge of clinical trial design and relevant disease indications to assist in study concept and protocol development. Contribute to discussions concerning scientific and procedural aspects of study design. Coordinate with departments to produce the final protocol and informed consent documents.</li><li>Contribute and review medical data review plans, Data Safety Monitoring Board (DSMB)/Safety Review Committee (SRC) charters, and specific sections of study manuals and investigator meeting materials.</li><li>Contribute to the development of CRFs, data edit checks, and/or patient profile design.</li><li>Conduct ongoing data cleaning (query generation, coding review, SAE reconciliation) and data trend analysis.</li><li>Lead internal clinical data review meetings in conjunction with the medical monitor, if applicable</li><li>Prepare slides as needed site calls and for dose escalation meeting, as applicable to study stage.</li><li>Coordinate with Medical Affairs and manage external medical advisory committees for the study team such as DSMBs and Scientific Steering Committees, in conjunction with the medical monitor.</li><li>Research and summarize published literature for continual learning and to prepare training materials for other clinical team members.</li><li>Contribute to statistical analysis plans, table, listing, figure design and the preparation of manuscripts and other presentations of study data, as appropriate.</li><li>Address investigator questions regarding protocol and related scientific issues and attend site initiation visits (SIVs), in coordination with the medical monitor.</li><li>Assist in determining the activities to support a project's priorities within functional area.</li><li>Up to 25% travel (US and International)</li></ul> Basic Qualifications Advanced degree in clinical or biological sciences (MD, PhD, or PharmD preferred) and 4+ year's (Associate Dir) or 8+ years (Director) relevant drug development experience with minimum of 3 years’ experience in oncology clinical trials. Preferred Qualifications<ul><li>Experience in the clinical science role, in an oncology indication for first-in-human and proof of concept studies in small molecules, biologics and/or cell therapy. Registrational or Phase 3 study experience is desired.</li><li>In depth understanding of clinical operations and translational medicine.</li><li>Excellent interpersonal and communication skills.</li><li>Able to translate technical concepts into accessible language and direction for the broader study team.</li><li>Excellent attention to detail, collaboration, and initiative, with flexibility to adapt to the needs of the organization; maintain meticulous attention to project deadlines.</li><li>Experienced in Microsoft Office (Excel, Word, PowerPoint, OneNote), and ideally also with job related programs such as Spotfire and Medidata Rave or similar.</li><li>Strong understanding of ICH GCP, as well as general knowledge of industry practices and standards</li><li>Commitment to patient safety and clinical compliance.</li></ul>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 (<a href="https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.nurixtx.com%2Fprivacy-policy%2F&data=05%7C01%7CEKwong%40nurixtx.com%7C598063b43c7346495d2908db8a013c96%7C1c966021d55145e489a5849f81b69208%7C0%7C0%7C638255510177936421%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=ZGFKSH61Un4AiGchAOr7elttfiKtOQB7huPs0DlQY54%3D&reserved=0" rel="no-follow nofollow">https://www.nurixtx.com/privacy-policy/</a>).

Nurix Therapeutics

Associate Director/Director, Clinical Science

Biology

Case Report Form (CRF)

Cell Biology

Clinical Data

Clinical Practices/Protocols

Clinical Research

Clinical Study Publications

Clinical Support

Clinical Trial

Code Reviews

Communication Skills

Cross-Functional

Data Analysis

Data Cleaning

Detail Oriented

Disease

Drug Development

GCP (Good Clinical Practices)

ICH Regulations

Industry Standards

Informed Consent

Interpersonal Skills

Medical Affairs

Medical Writing

Medicine

Microsoft Excel

Microsoft Office

Microsoft PowerPoint

Microsoft Word

New Drug Application

Oncology

Patient Assessment

Patient Safety

Pharmacovigilance

Proof of Concept

Reconciliation

Regulatory Submissions

Safety Compliance

Site Initiation

Small Molecules

Statistics

Strategic Planning

Team Player

Time Management

Trend Analysis

Willing to Travel

BioSpace

Clinical Trials Manager

Leveraging Nurix’s extensive expertise in E3 ligases together with its proprietary DNA-encoded libraries, Nurix has built DELigase, an integrated discovery platform to identify and advance novel drug candidates targeting E3 ligases, a broad class of enzymes that can modulate proteins within the cell. Nurix’s wholly owned pipeline comprises targeted protein degraders of Bruton’s tyrosine kinase, a B-cell signaling protein, and inhibitors of Casitas B-lineage lymphoma proto-oncogene-B, an E3 ligase that regulates T cell activation.

Nurix, Inc. is seeking a Clinical Trial Manager (CTM)/Sr. CTM to join the Clinical Operations team.  This individual will be responsible for management of assigned clinical trials and/or global regions. They will lead study team, vendors, clinical monitors and clinical sites throughout the life cycle of a clinical trial.This individual will be able to manage clinical regions and/or trial(s) and have broad involvement in work central to Nurix’s strategic goals. They will apply existing technical skills, learn new skills, and play a key role in clinical development of the programs.The CTM/Sr. CTM is responsible for the successful implementation of assigned clinical trial(s), independently, from start-up to close-out. Experience in managing cross-functional teams, vendor oversight, knowledge of applicable regulatory requirements and developing junior staff will be essential to the team's success. The CTM/Sr. CTM will represent Clinical Operations at Project team meetings and may represent Nurix at professional events. Job Responsibilities:<ul><li>Accountable for all operational aspects of assigned clinical trial(s) and/or geographical region.</li><li>Develop and implement clinical trial protocols, including study objectives, inclusion/exclusion criteria, and data collection procedures</li><li>Responsible for selection of vendors/CROs and provide effective ongoing management and oversight to vendors/CROs to ensure compliance and execution of deliverables within the approved budget, study timeline, and study protocol</li><li>Works closely with investigative site personnel, CROs, and other study vendors</li><li>Manage relationships with site investigators and study coordinators</li><li>Monitor and track clinical trial progress and provide status update to stakeholders</li><li>Monitor recruitment progress and effectively address enrollment challenges</li><li>Manage study contracting, budget, forecasting, accruals and payment process for all clinical trial vendors including investigational sites</li><li>Collaborate with Data Management to ensure correct CRFs content is collected, prepare/implement CRF completion guidelines, and coordinate delivery of data updates, listings and study reports</li><li>Drafts and coordinates review of relevant documents including protocols, informed consents, case report forms, monitoring plans and relevant study plans, investigator brochures and clinical study reports.</li><li>Prepare for and manage regulatory agency audits and inspections</li><li>Must be able to participate in cross-functional strategic initiatives under limited supervision</li><li>Proactively identifies potential issues/risks and recommends/implements solutions</li><li>Provides leadership to the clinical operations team working on the assigned clinical trials</li></ul> Experience and Skills<ul><li>B.S./ B.A. in biological sciences with 5+ years of relevant industry experience</li><li>Ability to travel as required for the program (25%)</li><li>Demonstrate knowledge of FDA, EMA, ICH and GCP regulations and guidelines</li><li>Experience managing global trials</li><li>Experience in leading teams, including CROs, consultants and vendors</li><li>Must display strong analytical and problem-solving skills at a project level and collaborate with colleagues to generate solutions</li><li>Strong communication and influence skills and ability to create a clear sense of direction</li><li>Ability to deal with time demands, incomplete information or unexpected events</li><li>Outstanding organizational skills with the ability to work independently, multi-task and prioritize</li><li>Comfortable in a fast-paced small company environment and able to adjust workload based upon changing priorities</li></ul> CompanyNurix Therapeutics is a biopharmaceutical company focused on the discovery, development and commercialization of small molecule therapies designed to modulate cellular protein levels as a novel treatment approach for cancer and immune disorders. Leveraging Nurix’s extensive expertise in E3 ligases together with its proprietary DNA-encoded libraries, Nurix has built DELigase, an integrated discovery platform to identify and advance novel drug candidates targeting E3 ligases, a broad class of enzymes that can modulate proteins within the cell. Nurix’s drug discovery approach is to either harness or inhibit the natural function of E3 ligases within the ubiquitin proteasome system to selectively decrease or increase cellular protein levels.Nurix’s wholly owned pipeline comprises targeted protein degraders of Bruton’s tyrosine kinase, a B-cell signaling protein, and inhibitors of Casitas B-lineage lymphoma proto-oncogene-B, an E3 ligase that regulates T cell activation. Nurix is headquartered in San Francisco, California.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 (<a href="https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.nurixtx.com%2Fprivacy-policy%2F&data=05%7C01%7CEKwong%40nurixtx.com%7C598063b43c7346495d2908db8a013c96%7C1c966021d55145e489a5849f81b69208%7C0%7C0%7C638255510177936421%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=ZGFKSH61Un4AiGchAOr7elttfiKtOQB7huPs0DlQY54%3D&reserved=0" rel="no-follow nofollow">https://www.nurixtx.com/privacy-policy/</a>).

Clinical Trial Manager (CTM)/Sr. CTM

Analysis Skills

Auditing

Brochures

Budgeting

Cancer

Candidate Sourcing

Clinical Monitoring

Clinical Trial Management

Contract Management

Contract Research Organization (CRO)

Data Collection

Data Management

Drug Discovery

Establish Priorities

FDA (Food and Drug Administration)

Forecasting

Identify Issues

Leadership

Lymphoma

Maintain Compliance

Multitasking

Organizational Skills

Problem Solving Skills

Regulations

Regulatory Requirements

Relationship Management

Research Protocols

Small Company

Startup

Team Lead/Manager

Vendor/Supplier Selection

Research Associate

CompanyNurix Therapeutics is a biopharmaceutical company focused on the discovery, development and commercialization of small molecule therapies designed to modulate cellular protein levels as a novel treatment approach for cancer and immune disorders. Leveraging Nurix’s extensive expertise in E3 ligases together with its proprietary DNA-encoded libraries, Nurix has built DELigase, an integrated discovery platform to identify and advance novel drug candidates targeting E3 ligases, a broad class of enzymes that can modulate proteins within the cell. Nurix’s drug discovery approach is to either harness or inhibit the natural function of E3 ligases within the ubiquitin proteasome system to selectively decrease or increase cellular protein levels.Nurix’s wholly owned pipeline comprises targeted protein degraders of Bruton’s tyrosine kinase, a B-cell signaling protein, and inhibitors of Casitas B-lineage lymphoma proto-oncogene-B, an E3 ligase that regulates T cell activation. Nurix is headquartered in San Francisco, California. PositionWe are seeking a highly motivated individual with a 2-4 years of lab experience with a background in purification of small molecule drug compounds by HPLC, milligram up to gram scale, to join the Analytical Chemistry group at Nurix located in The Woodlands, Texas.This position will perform purifications of small molecule libraries by mass directed HPLC and support our early drug discovery efforts at Nurix. The candidate requires the ability to work in a fast-paced laboratory setting using state of the art analytical equipment and cloud-based data systems. This role requires hands on experience in maintenance and troubleshooting of chromatography instrumentation. This role also requires basic lab / chemical handling safety and the ability to lift 40 lbs.The candidate should have a strong desire to learn new techniques, stay up to date with purification trends and an aptitude for robotic automation workflows. The ideal candidate will be self-driven, resourceful, organized, focused, and enjoy working in the dynamic team environment here at Nurix. Required Qualifications Minimum qualifications include a B.S. or equivalent degree in chemistry, analytical chemistry, or related field, with (2-4) years of industrial experience in analysis of small molecules, liquid chromatography, and mass spectroscopy. Bonus Qualifications Familiarity with Agilent ChemStation or similar chromatography software Fit with Nurix Culture and Values<ul><li>Strong team orientation; highly collaborative</li><li>Solutions and results-oriented focus</li><li>Hands-on approach; resourceful and open to diverse points of view</li></ul> 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. Note to Employment Agencies: Please do not forward any agency resumes. Nurix will not be responsible for fees related to unsolicited resumes.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 (<a href="https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.nurixtx.com%2Fprivacy-policy%2F&data=05%7C01%7CEKwong%40nurixtx.com%7C598063b43c7346495d2908db8a013c96%7C1c966021d55145e489a5849f81b69208%7C0%7C0%7C638255510177936421%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=ZGFKSH61Un4AiGchAOr7elttfiKtOQB7huPs0DlQY54%3D&reserved=0" rel="no-follow nofollow">https://www.nurixtx.com/privacy-policy/</a>).

Lab Senior Research Associate, Purification / Analytical Chemistry

Analytical Chemistry

Automation

Chromatography

Cloud Computing

Drug Compounds

High Performance Liquid Chromatography (HPLC)

Laboratory

Research Laboratory

Small Molecule Drugs

Chemist

Experience working with bioanalytical tools such as hydrophobic interaction chromatography (HIC), preparative-scale size exclusion chromatography (SEC), liquid chromatography-mass spectrometry (LC-MS), ion-exchange (IEX), and reversed phase (RP)-HPLC, Nuclear Magnetic Resonance (NMR) Spectroscopy. The successful candidate will have the opportunity to directly contribute to the following key platform operations: Develop, optimize and implement high-throughput bioconjugation processes through the application of established and state-of-the-art technologies.

PositionWe are seeking a talented and highly motivated scientist with a strong background and hands-on experience in bioconjugation to join our Discovery Chemistry team. In this laboratory-based position, you will play a pivotal role in the development of cutting-edge Degrader-Antibody Conjugates (DACs) across various therapeutic areas. The successful candidate will have the opportunity to directly contribute to the following key platform operations:<ul><li>Develop, optimize and implement high-throughput bioconjugation processes through the application of established and state-of-the-art technologies</li><li>Execute high-throughput preparation of novel antibody drug conjugates at milligram scale</li><li>Contribute to the design and synthesis of linkers and linker-payloads to enhance conjugate properties </li><li>Prepare, purity and characterize bioconjugates to support in-vitro and in-vivo studies</li><li>Contribute to the collaborative efforts focused on the development and optimization of bioanalytical protocols to evaluate critical quality attributes of DACs </li><li>Engage in cross-functional discussions and contribute to scientific strategies and team goals focused on advancing Nurix’s Degrader-Antibody Conjugate (DAC) discovery programs</li><li>Prepare reports and present data at internal group meetings</li></ul> Education and Experience<ul><li>Ph.D. in Organic Chemistry, Chemical Biology, Biochemistry, or related field with up to 4 years relevant experience OR MS with 6+ years relevant experience, OR BS or equivalent with 10+ years relevant experience</li><li>Experience with high-throughput automated workflows to produce bioconjugates</li><li>Hands-on laboratory experience in carrying out diverse conjugation chemistry protocols, linker-payload synthesis and related processors to produce high-quality drug conjugates</li><li>Familiar with the general workflow operations, instrumentation and practices used for the generation of antibody-drug conjugates</li><li>Experience characterizing and purifying bioconjugates using common analytical tools</li><li>Experience working in the drug discovery chemistry field – linker design, synthesis, and SAR based property optimization of small molecules</li><li>Established track record of conference presentations and peer-reviewed publications in the areas of antibody drug conjugation and organic synthesis</li><li>Strong written and verbal communication skills</li></ul> Added Quantifications<ul><li>Postdoctoral or industrial work experience in the bioconjugation field</li><li>Experience working in Antibody-Drug Conjugate (ADC)- or Degrader-Antibody Conjugate (DAC)- based drug discovery programs</li><li>Experience working with bioanalytical tools such as hydrophobic interaction chromatography (HIC), preparative-scale size exclusion chromatography (SEC), liquid chromatography-mass spectrometry (LC-MS), ion-exchange (IEX), and reversed phase (RP)-HPLC, Nuclear Magnetic Resonance (NMR) Spectroscopy</li><li>Experience carrying our assays to evaluate in-vitro stability of ADC and payloads such as Cathepsin B, esterase activity and free drug analysis</li></ul> Fit with Nurix Culture and Values<ul><li>Strong team orientation and highly collaborative</li><li>Solutions and results-oriented focus</li><li>Hands-on approach; resourceful and open to diverse points of view</li></ul>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 (<a href="https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.nurixtx.com%2Fprivacy-policy%2F&data=05%7C01%7CEKwong%40nurixtx.com%7C598063b43c7346495d2908db8a013c96%7C1c966021d55145e489a5849f81b69208%7C0%7C0%7C638255510177936421%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=ZGFKSH61Un4AiGchAOr7elttfiKtOQB7huPs0DlQY54%3D&reserved=0" rel="no-follow nofollow">https://www.nurixtx.com/privacy-policy/</a>).

Scientist I – Bioconjugate Chemist (Contractor) – Discovery Chemistry

Antibodies

Assays

Biochemistry

Chemistry

High Throughput

Instrumentation

Leading Edge Technology

Liquid Chromatography-Mass Spectrometry (LC-MS)

Nuclear Magnetic Resonance

Nuclear Magnetic Resonance Spectroscopy

Organic Chemistry

Presentation/Verbal Skills

Protocol Analysis

Publications

Reporting Skills

Reversed Phase HPLC

Securities and Exchange Commission (SEC)

Wheel/Front-End Loader

Writing Skills

Biotech Scientist

CompanyNurix Therapeutics is a biopharmaceutical company focused on the discovery, development and commercialization of small molecule therapies designed to modulate cellular protein levels as a novel treatment approach for cancer and immune disorders. Leveraging Nurix’s extensive expertise in E3 ligases together with its proprietary DNA-encoded libraries, Nurix has built DELigase, an integrated discovery platform to identify and advance novel drug candidates targeting E3 ligases, a broad class of enzymes that can modulate proteins within the cell. Nurix’s drug discovery approach is to either harness or inhibit the natural function of E3 ligases within the ubiquitin proteasome system to selectively decrease or increase cellular protein levels.Nurix’s wholly owned pipeline comprises targeted protein degraders of Bruton’s tyrosine kinase, a B-cell signaling protein, and inhibitors of Casitas B-lineage lymphoma proto-oncogene-B, an E3 ligase that regulates T cell activation. Nurix is headquartered in San Francisco, California. Position DescriptionNurix is seeking a Senior/Principal Scientist, Pharmaceutical Development to provide scientific, technical, and hands-on leadership of small molecule oral solid formulation development for pre-clinical through Phase 1 clinical trial stages. Responsibilities will include but are not limited to:<ul><li>Lead small molecule preclinical and clinical formulation development and characterization in support of internal Nurix development programs</li><li>Manage outsourced development projects and manufacturingincluding timeline and resource planning, to ensure milestones and deliverables are met efficiently</li><li>Partner with Nurix Chemical Development and Analytical Development to identify optimal drug substance properties and control strategies</li><li>Oversee preparation and characterization of pre-clinical drug products for in-house and partner with Global Supply Chain Operations for outsourced studies and clinical manufacturing</li><li>Serve as drug product SME for cross-functional project teams</li><li>Author and review relevant sections of regulatory filings, technical protocols, reports, ect.</li><li>Manage and mentor research associates</li><li>Contribute to internal and external presentations and publications.</li></ul>   Required Qualifications<ul><li>In-depth knowledge and demonstrated expertise and accomplishment in oral solid dose form, characterization, manufacturing process development, and Phase I clinical manufacturing</li><li>Significant experience with design, scale-up, and outsourced manufacture of amorphous solid dispersion-based formulations design (spray drying, hot melt extrusion, tableting and encapsulation); experience with other enabled oral formulations a plus</li><li>Prior experience in formulation of targeted protein degrader molecules (aka CTMs, degraders, PROTACS) a plus</li><li>Thorough understanding of analytical techniques used for pre-formulation and characterization of oral solid dose forms including HPLC, LC-MS, XRPD, DSC, Dissolution, and KF</li><li>Excellent technical problem solving and troubleshooting abilities</li><li>Excellent written and oral communications skills</li><li>PhD (preferred) or MS in chemistry, pharmaceutics, engineering, or related field with at least 7 years relevant industrial experience</li><li>Ability to travel up to 25% of time</li></ul>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 (<a href="https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.nurixtx.com%2Fprivacy-policy%2F&data=05%7C01%7CEKwong%40nurixtx.com%7C598063b43c7346495d2908db8a013c96%7C1c966021d55145e489a5849f81b69208%7C0%7C0%7C638255510177936421%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=ZGFKSH61Un4AiGchAOr7elttfiKtOQB7huPs0DlQY54%3D&reserved=0" rel="no-follow nofollow">https://www.nurixtx.com/privacy-policy/</a>).

Senior/Principal Scientist, Pharmaceutical Development

Analytical Development

Drug Products

Extrusion

Manufacturing

Manufacturing/Industrial Processes

Medical Products

Mentoring

Outsourcing

Pharmaceutics

Phase I Clinical Trials

Pre-Clinical

Pre-Clinical Development

Process Development

Supply Chain Operations

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