104 Results for

Regulatory Affairs Jobs in Presidio, CA

Jobs

New!

San Francisco, CA1 day ago

Remote

The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. Consistently acts to enhance Jazz Pharmaceuticals’ image as an advocate of medical advancement by using knowledge of product, disease state and pipeline products to engage healthcare providers in meaningful scientific exchange of information.

Mountain View, CA30+ days ago

$75,000–$95,000 Per Year

Perform and document Complaint Handling, assessment, and reporting Receive and investigate product- and service-related communications / complaints, with communication received from various sources, including communications from field service management platforms (ServiceMax), customer relationship management platforms (SalesForce), enterprise resource planning platforms (Business Central), internal service records, and other direct and indirect customer/user communications. Regulatory Affairs (Associate / Specialist / Senior Specialist) Post Market Surveillance personnel are responsible for: (1) analyzing Post Market Surveillance (PMS) data to prepare Post Market Surveillance reports and documentation, and to update related risk and other documentation accordingly.

New!

Emeryville, CAToday

Commit to creating and demonstrating inclusivity within Vituity including codesigning, building, and executing strategies, policies, and practices that cultivate equity, inclusion, and fair opportunity for all; demonstrating preparedness to educate, mitigate, coach, and address daily bias and exclusion in partnership with the site leadership. Accountable for ensuring meaningful integration occurs: Identify opportunities for practice line integration to ensure the quality and efficiency of patient care delivery across the acute care continuum; assist with new service line startups; engage regularly with integrated site RDs.

South San Francisco, CA9 days ago

Remote

$170,000–$210,000 Per Year

Reporting to the Senior Director, Regulatory Affairs, this position will serve as a core regulatory representative on cross‑functional program teams, supporting interactions with global health authorities and ensuring regulatory strategies and submissions are aligned with evolving regulatory expectations for cell and gene therapies. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of “off-the-shelf” CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients.

New!

Oakland, CA1 day ago

$115,000–$130,000 Per Year

Through partnerships with global supply chains and community organizations, SupplyBank.org provides a highly cost-effective and scalable mechanism for bulk purchasing and efficiently distributing necessary health, education, and emergency supplies to children, families, and communities that need them throughout California. Of the total 100 acres, more than 80 will be revitalized park spaces, infrastructure improvements and nature based solutions to restore tidal wetlands, habitat, flood management and increase public enjoyment of the Bay Trail and parklands.

Berkeley, CA7 days ago

$200,000–$235,000 Per Year

The company is developing its lead candidate RTx-015 in retinitis pigmentosa, a degenerative retinal disease with significant unmet medical need as well as a pipeline to treat both rare and large market indications. RayTx is using a novel bioengineered optogenetic protein optimized for human vision delivered by AAV to restore visual function in a mutation agnostic approach and without the need for light enhancing eyewear.

Palo Alto, CA11 days ago

$185,000–$205,000

Contributes to the development of global clinical and regulatory plans and strategies, identifies and proposes risk mitigation strategies, and influences project teams and sub teams across international site locations. Do you want to be part of building a fully integrated biopharmaceutical company together with a team of highly skilled colleagues who are passionate about developing best-in-class therapeutics that address significant unmet medical needs?

Palo Alto, CA30+ days ago

$145,000–$167,000 Per Year

Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health technology company that has redefined brain imaging with the Swoop®system—the first FDA-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of care in a healthcare facility. Assess and advise regulatory strategies to optimize business expectations related to domestic and international commercial product availability and regulations:Anticipate regulatory obstacles and emerging issues throughout the product lifecycle and develop solutions.

Mountain View, California30+ days ago

$80,000–$80,000

Ultimate Staffing Services is actively seeking a dedicated and detail-oriented Regulatory Affairs Associate to join a reputable medical device manufacturer. Coordinate, prepare, compile, and maintain regulatory documentation for local and regional registration, license renewal, and product submissions.

San Francisco, CA7 days ago

Provide regulatory review and input for key development documents, including clinical protocols, statistical analysis plans, and clinical and nonclinical study reports, ensuring alignment with regulatory expectations. Represent Regulatory Affairs for assigned programs by providing regulatory guidance, identifying potential risks, and supporting the execution of regulatory plans.

Richmond, CA30+ days ago

Full-time

Knowledge of current Good ClinicalPractices (cGCP), current Good Manufacturing Practices (cGMP), Good Documentation Practices and a strong understanding of FDA regulations and guidelines. Participate in review of BabyBIG documentation to support highest possible quality of all records produced by manufacturing contractors or contracting research organizations .

San Francisco, CA7 days ago

The organization is advancing multiple programs across early and late-stage development and is building out its Regulatory CMC leadership to support global filings and accelerate programs toward commercialization. This is a high-impact, strategic leadership role for someone who thrives at the intersection of regulatory strategy, CMC development, and cross-functional program execution in a fast-paced, science-driven environment.

SF, CA30+ days ago

POSITION SUMMARY:The Senior Regulatory Affairs & Compliance Specialist is responsible for ensuring compliance with regulatory, licensing, and contractual requirements set forth by the Centers for Medicare and Medicaid Services (CMS), the California Department of Health Care Services (DHCS), and other regulatory agencies. Seniors, their family members, and caregivers face many issues, including transportation to appointments, management of medications, coordination of medical care from different specialists, lack of social interaction, and ability to stay alone at home.

South San Francisco, CA7 days ago

In partnership with Regulatory Project Management, Regulatory Labelling and Regulatory CMC, oversees the development of content and format for regulatory submissions and related variations/amendments internationally in assigned TA. Leads the Global Regulatory Project Team meetings in collaboration with Regulatory Project Management when being the Global Regulatory Lead on a project.

Alameda, CA27 days ago

Remote

$140–$155 Per Hour

Serve as a key cross-functional partner across Research & Development, Quality Assurance, Pharmaceutical Supply Chain, and Information Technology to drive enterprise-wide implementation of regulatory expectations. RequirementsBachelor’s degree in a related discipline with minimum of thirteen years of relevant experience; or master’s degree with at least eleven years; or PhD with at least eight years; or equivalent education and experience.

Alameda, California20 days ago

Remote

$85–$93.68 Per Hour

Collaborate with Quality Assurance and cross‑functional stakeholders to support health authority inspections across GPS and Regulatory Affairs, ensuring the RA function remains in a continuous state of inspection readiness. · Work with Regulatory Affairs Strategist, CRO and Clinical Operations to ensure the Trial Master File (TMF) and Veeva RIM is kept current and complete for Regulatory Affairs-related documents.

Alameda, California27 days ago

$133.33–$153.33 Per Hour

Bachelor's degree in related discipline and a minimum of thirteen years of related experience; or, · Master's degree in related discipline and a minimum of eleven years of related experience; or, · PhD degree in related discipline and a minimum of eight years of related experience; or, · Equivalent combination of education and experience. Leads the systematic collection, analysis, and dissemination of regulatory intelligence to proactively inform our client's policies, processes, and practices, enabling subject matter experts to assess the impact of evolving global regulatory requirements and translate regulatory changes into actionable guidance.

San Francisco, CA7 days ago

Remote

This full-time role offers a competitive salary and excellent benefits, contributing to life-changing healthcare solutions.#J-18808-Ljbffr. You will develop and execute regulatory strategies, manage FDA submissions, and ensure compliance for innovative medical devices.

South San Francisco, CA30+ days ago

$276,000–$345,000

Collaborate with cross-functional teams (Clinical Development, CMC, Quality Assurance) to ensure regulatory compliance throughout the development process and ensure cross-functional alignment during key steps across multiple projects simultaneously. We are seeking a strategic and results-oriented leader to oversee all regulatory activities for our hematology/immunology pipeline, with an initial focus on the upcoming Phase 3 clinical trial for our lead candidate, VGA039.

Los Altos, CA30+ days ago

Remote

$140,000

You will operate as a core member of Bidgely’s Regulatory Affairs function, working closely with internal partners across Sales, Go-to-Market, Product, and Engineering to ensure regulatory strategy actively supports customer adoption and market expansion. You will: Monitor and analyze state-level regulatory proceedings, legislation, and utility plans related to grid modernization, data analytics, demand-side management, energy efficiency, and customer experience.

Palo Alto, CA30+ days ago

The Associate Director ensures will be working on biostatistics deliverables, including study design, data analysis, data mining, epidemiology-related analyses, use of clinical trial data to inform reimbursement strategy and HTA, real world evidence, quality of life data, and interpretation, reporting, and publication of results. The Associate Director, Medical Affairs Statistical Sciences Biometrics provides technical and operational support for the design, implementation and interpretation of post approval clinical trials, programs, and disease registries.

San Francisco, CA30+ days ago

$225,000

Strategic Client Leadership & Outcomes - You will serve as the senior strategic contributor to C-suite and executive leaders within the technology sector, guiding them through complex challenges related to corporate reputation, public affairs, and market positioning. We apply our unique expertise across strategic communications, public affairs, research, and digital marketing to create sophisticated and customized strategies that make change possible for both American and European clients.

New!

Redwood City, California5 days ago

Operating as a senior enterprise leader and trusted advisor to the Board, CEO, Executive Team, and senior leadership, the PPGA Leader integrates geopolitical intelligence, regulatory foresight, and systems‑level thinking to anticipate threats and opportunities, and to develop coordinated offensive and defensive strategies that protect and advance the Company’s interests worldwide. Lead the development of a coherent, multi‑year global PPGA strategy, in close partnership with a cross‑functional leadership team, ensuring alignment with the Company’s overall corporate and regional strategies.

Palo Alto, CA13 days ago

Full-time

In addition, Academic Deans serve as key ambassadors of the academic program—partnering in admissions, contributing to school communications, and helping to represent INTL’s educational vision to current and prospective families. This position also requires the employee to remain on campus for one (1) week following the conclusion of the academic year and to return to campus one (1) week prior to the regular faculty return date in order to support back-to-school planning, preparation, and related activities.

San Francisco, CA30+ days ago

$300,000–$360,000 Per Year

Advance collaborations with Key Opinion Leaders and establish robust partnerships within the medical and scientific community, including oversight of KOL interactions, advisory board strategy, academic partnerships, and professional society activities to generate actionable insights. Provide cross-functional leadership and strategic input across clinical development, clinical operations, regulatory affairs, commercial, market access, and pharmacovigilance to inform product development strategies and commercial planning.

San Francisco, CA9 days ago

YES Under guidance of Vice Dean and Assistant Dean for Administration and Finance, develops and implementssolutions with high level stakeholders such as faculty, senate committee chairs, senior administrators, , to develop solutions to complex problems; providing briefings on key issues. YES Providing strategic oversight for the development of the annual, faculty compensation; determining priorities, recommending and implementing changes to methods, unit planning, staffing, programs and other financial activities.

Walnut Creek, CA30+ days ago

$105,000–$115,000 Per Year

You'll play a key role in building our organic certification programs and supporting our partnerships with our CoMan network and major retailers like Walmart and Costco. Most of our work happens in the office to spark creativity and community, but we also offer flexibility so team members have the autonomy to work outside the office when needed to support their work-life balance and personal commitments.

Palo Alto, CA30+ days ago

$160,000–$175,000

A minimum of 8 years of experience: 5 years in drug, biologic and/or combination products in Regulatory Affairs and 3 years of experience performing directly relevant Regulatory Project Management activities within the pharmaceutical and/or biotechnology industries. Collaborate with Global Regulatory Affairs Leadership in establishing and managing timelines for key project milestones, adhering to processes and documentation, and communicating with cross-functional teams or key stakeholders within and across regions to ensure the delivery of business objectives.

San Francisco, CA12 days ago

Full-time
Employee

Note: By applying to this position you will have an opportunity to share your preferred working location from the following: San Francisco, CA, USA; Mountain View, CA, USA; Seattle, WA, USA; Washington D.C., DC, USA.Minimum qualifications: JD, LL.B., equivalent degree, or equivalent practical experience. As an Associate Regulatory Counsel in Privacy, you will join a Global team that provides subject matter expertise and engages with regulators and others to consider the role of privacy law in the changing economy, development of new technology, and passage of new laws and regulations.

San Francisco, CA30+ days ago

$142,500–$199,000 Per Year

These include the preparation and compilation of submissions for regulatory agencies across assigned clinical studies and programs, management of regulatory submission processes and timelines, and oversight of regulatory tracking tools, archives, and infrastructure. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple dual-masked T-cell engagers across validated targets in solid tumor indications.

Newark, CA20 days ago

$117,000–$143,000 Per Year
Full-time

Experience administering and/or supporting regulatory systems such as Veeva Vault RIM, particularly Registrations and regulatory data management, or submission publishing toolsExperience supporting global regulatory submissions and product registration trackingStrong understanding of regulatory operations and regulatory document lifecycleExperience working in GxP regulated environmentsStrong attention to detail with focus on data integrity and complianceExcellent organizational, communication, and cross-functional collaboration skillsExperience supporting system implementations, configuration, or upgrades is preferredCertification or training in Veeva Vault platformThe anticipated annualized base pay range for this full-time position is $117,000 - $143,000. The Regulatory Systems Manager will play a key role in improving processes, ensuring data integrity, supporting system implementations, configuration, or upgrades, and enabling efficient regulatory submissions and compliance.

Palo Alto, California30+ days ago

$186,000–$232,500 Per Year

New!

San Francisco, CA6 days ago

Additionally you must excel at communicating complex regulatory matters to engineering teams, driving compliant designs from early development phases, and make sound technical decisions that balance innovation with compliance requirements. You must be highly analytical, able to work effectively across multiple teams and have a strong ability to navigate the global regulatory compliance schemes to enable market access of consumer electronic products.

New!

Mountain View, CA6 days ago

$27–$30 Per Hour

With 850+ global consultants, VARITE is committed to delivering excellence to its customers by leveraging its global experience and expertise in providing comprehensive scientific, engineering, technical, and non-technical staff augmentation and talent acquisition services. Eligible employees may receive: Health Insurance: Medical, dental, and vision coverage Retirement Plans: Participation in a company-sponsored retirement savings plan Legal Service Plans – Offering access to attorneys for legal advice and representation If this opportunity interests you, please respond by clicking on EasyApply.

Berkeley, CA30+ days ago

$220,000–$235,000 Per Year

Provide Clinical Quality Assurance (GCP) strategic and technical leadership and Subject Matter Expertise (SME) to clinical study teams; Partner with the teams to effect appropriate and timely documentation of quality event management, including CAPA plans in support of product pipeline. The successful candidate must have the ability to execute QA tasks independently; effectively represent QA in a GCP, PV, and GLP focused team settings and manage quality related activities related to clinical vendors, investigator sites and regulatory agencies.

Sunnyvale, CA7 days ago

The Vice President of Trade Compliance reports to the SVP Planning and Logistics and is responsible for establishing, governing, and enforcing the company’s global trade compliance framework for medical devices, instruments, accessories, capital equipment, service parts, software, and indirect materials. Establish and maintain global policies covering: HS classification, Valuation, ECCN determinations, Country-Of-Origins and substantial transformation analysis, Free Trade Agreements and preferential duty programs, sanctioned, and denied party screenings for institutions and distributors.

New!

Alameda, CA6 days ago

$80–$100 Per Hour

Maintain current and complete Trial Master Files (TMF) and Veeva RIM related documents, working with relevant teams. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.

South San Francisco, CA30+ days ago

$200,000–$230,000
Full-time

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. 2. Leading the quality team in the execution of quality assurance activities, including inspection, testing, and auditing of our products to ensure they meet all required specifications.

Mountain View, CA30+ days ago

$175,000–$240,000

This role operates at the critical intersection of hardware, software, and regulatory compliance, managing a portfolio spanning backend integrations, operational control interfaces, and core drone operation systems. Excellent technical aptitude, with the ability to reason about cloud architectures, distributed systems, APIs, and operational tradeoffs, and communicate effectively with engineering teams.

South San Francisco, CA30+ days ago

$156,000–$195,000

As an Associate Director, the candidate is expected to represent translational sciences as a translational medicine lead for clinical studies and work closely with the clinical development team members including bioanalysis, clinical operations, regulatory affairs, quality, medical writing, safety, clinical research and clinical leadership. As part of the collaborative research team role, the candidate is expected to work with individuals across research and translational research groups, including discovery research, drug development and protein sciences, preclinical bioanalysis and other junior staff within translational research organization.

Daly City, California30+ days ago

Collaborates with the CNO and directs and participates in the preparation and administration of nursing services, budgets and capital outlay requests; evaluates staffing, equipment and supply needs; prepares justifications and cost benefit analyses; reviews and recommends approval of expenditures; oversees the procurement of supplies and equipment for assigned areas. Conduct on-going surveillance using Center of Disease Control (CDC) infection criteria, documentation, and investigation of nosocomial infections through review of admission diagnoses, microbiology culture results, isolation orders, patient records, consultation requests, post-discharge surveillance, and autopsy findings.

San Francisco, CA30+ days ago

$90,000–$105,000 Per Year

SFHP is chosen by eight out of every ten San Francisco Medi-Cal managed care enrollees and its 175,000+ members have access to a full spectrum of medical services including preventive care, specialty care, hospitalization, prescription drugs, and family planning services. Established in 1997, San Francisco Health Plan (SFHP) is an award-winning, managed care health plan whose mission is to provide affordable health care coverage to the underserved low and moderate-income residents in San Francisco County.

Palo Alto, CA24 days ago

$165,000–$175,000

Additional activities may include but are not limited to: Maintains strong relationships and communication with key stakeholders, including Commercial leadership, and GPS leadership to address queries, share metrics, and discuss new program-related processes. Oversee the vendors/service providers to ensure that they fulfill their accountabilities and responsibilities, which in includes, but is not limited to: Responsible for assigned PV activities/projects and working collaboratively with other teams within Ascendis.

San Francisco, CA30+ days ago

Remote

$229,562–$344,342 Per Year

The role oversees a high-impact team and partners cross-functionally and externally to drive an integrated publications and scientific communications strategy, translating complex data into compelling evidence that supports clinical adoption, informs healthcare decision-making, and differentiates the company’s portfolio globally. Agios Pharmaceuticals is searching for a dynamic Senior Director, Global Scientific Communications and Publications expert to join our Global Medical Affairs team and lead a high-functioning communications/publications/congress team.

New!

Alameda, CA6 days ago

$80–$100 Per Hour

System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. Maintain current and complete Trial Master Files (TMF) and Veeva RIM related documents, working with relevant teams.

South San Francisco, CA30+ days ago

$336,000–$405,000 Per Year

Reporting to the Chief Medical Officer (CMO), the Vice President, Clinical Development provides executive leadership for the company’s clinical research and development activities within designated therapeutic areas and/or programs. The Vice President, Clinical Development serves as a senior leader within Clinical Development, accountable for clinical trial execution, data integrity, regulatory readiness, and cross-functional alignment.

South San Francisco, CA11 days ago

Remote

$200,000–$250,000 Per Year

Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of “off-the-shelf” CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients. 2+ years experience as a hematology/oncology or cell therapy MSL or similar role within the pharmaceutical or biotech industry or 4+ years experience as a direct patient care provider in a hematology/oncology or cell therapy program.

Dublin, CA30+ days ago

Full-time

Minimum of 3 years of paid work experience, with at least one year of paid work experience in the past three years, related to the distribution or dispensing of dangerous drugs or dangerous devices in a licensed pharmacy, drug wholesaler, drug distributor, or drug manufacturer. The role also contributes to cross‑functional planning initiatives, driving process improvements, implementing scalable solutions to complex operational challenges, and supporting long‑term regional and global transformation projects as needed.

South San Francisco, CA11 days ago

Remote

$200,000–$250,000 Per Year

Drive Medical Communications (MC) for assigned pipeline assets in partnership with internal stakeholders and external vendors/agencies, including development of the scientific platform and creation/review of scientific communication deliverables (e.g., slide decks, congress materials, FAQs, field medical materials) through MRC review and warehousing. This role will be accountable for defining and executing the global medical information and scientific communications strategy, establishing operational excellence, and ensuring compliant, high-impact scientific exchange aligned with Allogene’s mission to advance allogeneic CAR-T therapies for patients with serious diseases.

New!

South San Francisco, CA1 day ago

Remote

$360,000–$425,000 Per Year

Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of “off-the-shelf” CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients. Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease.

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Regulatory Affairs Jobs in Presidio, CA

Medical Science Liaison, Oncology (Northern CA, OR, WA, MT, ID) Jazz Pharmaceuticals

Regulatory Affairs - Post Market Surveillance Iridex Corporation

Regional Director - Anesthesiology - Vituity Practice Management - Emeryville Vituity

Associate Director, Regulatory Affairs Allogene Therapeutics

Director of Regulatory Affairs and Policy SupplyBank.org

Director of Regulatory Affairs Ray Therapeutics

Associate Director, Global Regulatory Affairs Clinical Strategy - Job ID: 1961 Ascendis Pharma

Senior Regulatory Affairs Specialist Hyperfine

Regulatory Affairs Associate Jess Bushey

Senior Manager Regulatory Affairs Warman O'Brien

Regulatory Affairs Coordinator Public Health Foundation Enterprises, In

Director Regulatory Affairs CMC Meet Life Sciences

Snr Regulatory Affairs & Compliance Specialist PACE On Lok

Senior Director Regulatory Affairs Scientific Search

Regulatory Affairs Strategy Director Joulé

Regulatory Affairs Quality/Standards/Training Manager - Remote Roth Staffing Companies

Regulatory Affairs Strategy Director Roth Staffing Companies

Regulatory Affairs Lead AI & SaMD (Remote) El Camino Health

VP. Regulatory Affairs Star Therapeutics

Manager, Regulatory Affairs & Market Development Bidgely Inc.

Associate Director, Medical Affairs Statistical Sciences, Biometrics - ID: 1799 Ascendis Pharma

Managing Director, Public Affairs & Strategic Communications (Technology) Bully Pulpit International

VP Public Policy & Government Affairs Equinix

French Academic Dean & Director of French Affairs Silicon Valley International School

Vice President, Medical Affairs Vir Biotechnology

Senior Consultant, Academic Affairs University of California , San Francisco

Sr. Regulatory Documentation Control Specialist - Organic Kinder's

Senior Manager, Regulatory Project Manager - Job ID: 1820 Ascendis Pharma

Associate Regulatory Counsel, Privacy Google

Senior Manager, Regulatory Operations Vir Biotechnology

Regulatory Systems Manager Ardelyx

Manager, ADS Safety Case, Regulatory Rivian

Sr. HW Regulatory Compliance Engineer, eero Amazon

Regulatory Compliance Test Engineer Varite

Director of Quality Assurance, Clinical Caribou Biosciences, Inc.

VP of Trade Compliance Gateway Recruiting

Temporary Senior Manager Compliance System One Holdings, LLC

Director of Quality Jobot

Product Manager, Platform Matternet

Associate Director, Translational Science Star Therapeutics

ASSOCIATE CNO AHMC Healthcare

Program Manager, NCQA San Francisco Health Plan

Senior Manager, PV Vendor Management Team - Job ID: 1946 Ascendis Pharma

Senior Director, Global Scientific Communications and Publications - Remote Agios Pharmaceuticals

Temporary Senior Manager Compliance System One

Vice President, Clinical Development Rigel Pharmaceuticals, Inc.

Director, Medical Science Liaison (Northeast US and Canada) Allogene Therapeutics

Supply Chain Compliance & Planning Manager Zeiss Group

Director, Global Medical Information & Scientific Communications Allogene Therapeutics

Vice President, Clinical Development (Oncology) Allogene Therapeutics

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