77 Results for

Regulatory Affairs Jobs in Larkspur, CA

Jobs

New!

San Francisco, CA3 days 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.

New!

Emeryville, CA2 days ago

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.

New!

Oakland, CA3 days 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.

South San Francisco, CA11 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.

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 .

Alameda, California22 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, California29 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.

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, 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.

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.

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.

New!

San Mateo, CA1 day ago

$330,000–$405,000 Per Year

Seamlessly partner with all business partners within Freshworks, including but not limited to Sales, Professional Services, Sales Operations, Deals Desk, Finance, Product, Partner & Alliances, Marketing and Information Security, to proactively identify and address risks and opportunities, helping Freshworks move quickly to execute company business objectives while ensuring legal considerations are integrated into such business decisions. Reporting to the Chief Legal Officer, this role requires a collaborative and pragmatic team playerwho can proactively lead the global commercial legal team, navigate escalations, design legal operations and drive and manage multiple complex customer negotiations and commercial projects through to completion.

South San Francisco, CA7 days ago

$19.05–$34.06 Per Hour

Responsibilities include synthesizing regulatory data into structured intelligence reports, maintaining regulatory databases, supporting dashboards and reporting tools, and ensuring audit-ready documentation. The Regulatory Intelligence Specialist supports global Regulatory Intelligence operations by monitoring, analyzing, and disseminating regulatory updates impacting pharmaceutical and biotech development programs.

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.

San Francisco, CA14 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.

Newark, CA22 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.

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.

San Francisco, CA30+ days ago

You will oversee the preparation and submission of regulatory documents, manage relationships with regulatory agencies, and lead cross-functional teams to support regulatory activities across a variety of projects and therapeutic areas. Oversee and coordinate cross-functional project teams to compile data for regulatory submissions and manage timelines for all regulatory deliverables.

Foster City, CA16 days ago

$72.72–$77.42 Per Hour

Job Description: The RWE Analyst will contribute to the Kite Real-World Evidence/Health Economic Outcomes Research (RWE/HEOR) Team as part of an effort to contribute to the strategies of the broader Kite Evidence Generation Team, which will include the conduct of timely, relevant, and rigorous analysis of real-world data (RWD) to address critical research questions and contribute to cross-functional initiatives. The RWE Analyst will be responsible for developing, reviewing, and providing feedback on study documents, such as protocols and statistical analysis plans, and executing planned data analyses using administrative claims, electronic health record (EHR), and observational registry databases.

Fairfield, California30+ days ago

Bachelor’s degree in relevant field preferred or equivalent combination of education and experience; minimum of two (2) years’ experience as a Regulatory Affairs Specialist or relevant experience in managed care with knowledge of the Medi-Cal, and NCQA requirements, and preferably Medicare and Knox Keene. Overview: The Regulatory Affairs Specialist II has demonstrated competencies in supporting the plan-wide regulatory affairs and compliance program, including activities related to HIPAA and Fraud, Waste, and Abuse (FWA).

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.

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.

South San Francisco, CA30+ days ago

$200,000–$230,000
Full-time

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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.

South San Francisco, CA30+ days ago

$190,000–$225,000 Per Year

Protocol Development and Study Oversight: Responsible for development of study protocols, case report forms (CRFs), consent forms, investigators brochure, development of charters (e.g., Independent Data Monitoring Committee, Safety Monitoring Committee) and other essential trial documents. Lycia Therapeutics is a biotechnology company using its proprietary lysosomal targeting chimera (LYTAC) platform to discover and develop best-in-class therapeutics that degrade extracellular and membrane-bound proteins.

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

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.

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, CA13 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.

South San Francisco, CA13 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.

Brisbane, California21 days ago

$224,000–$308,000 Per Year

Digital & Omnichannel Execution: Partner with the Omnichannel function to oversee the design and execution of omnichannel campaigns, including HCP and patient journeys, email marketing, websites, social media, digital media buying, and content syndication. The role requires a data-savvy, visionary marketer who can orchestrate personalized, scalable campaigns across personal and nonpersonal channels to drive commercial success in the highly competitive osteoarthritis category.

San Francisco, CA30+ days ago

Full-time

Vendor ManagementManage the third-party risk management program, ensuring that third-party relationships are adequately assessed for sufficient controls (especially information security), risks and aligned with the credit union’s strategic goals. Today, the San Francisco-based credit union has grown to $1.7B in assets and a membership that extends from the regional firefighters we trace our roots back to throughout our many neighbors in San Francisco, San Mateo and Marin Counties.

New!

South San Francisco, CA3 days 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.

San Francisco, CA30+ days ago

They are currently seeking a highly skilled and experienced Director of Biostatistics to provide leadership to develop and execute statistical strategy, design and analyses for clinical trials in all phases. Comprehensive and detailed knowledge of: statistical experimental designs, analyses and clinical trial requirements, particularly pertaining to Oncology trials.

South San Francisco, CA11 days ago

$240,000–$280,000

The Senior Director will collaborate closely with Clinical Development, Translational Medicine, Biomarker Sciences, Regulatory Affairs, Data Management, Statistical Programming, Clinical Operations, and external partners. The successful candidate will play a critical role in advancing precision medicine strategies through innovative trial methodologies, biomarker-driven development, and global regulatory engagement.

New!

South San Francisco, CA3 days ago

Remote

$250,000–$335,000 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. Participate in the authoring of relevant safety sections of clinical protocols, Investigator's Brochure (IB), informed consent form (ICF), statistical analysis plans, study reports and other clinical study-related documents to ensure alignment with the safety strategy and risk communication.

San Francisco, CA30+ days ago

$90,000–$100,000

As a trusted third party, we've facilitated over US$7 Billion in secured transactions, including high-profile domain names (like uber.com, snapchat.com, spacex.com, twitter.com, instagram.com), motor vehicles, business acquisitions, electronics and more. Hands-on experience managing one or more core compliance areas, such as transaction monitoring, licensing and renewals, regulatory filings, surety bond renewals, program documentation, or data privacy compliance.

Brisbane, California9 days ago

$224,000–$300,000 Per Year

Business areas supported include: research and development, clinical trials (commercial products and potential pipeline products), medical affairs, market access, corporate communications, global supply chain and quality, manufacturing, commercial sales and marketing to healthcare providers, patients and payers (including U.S. Federal Government), business development, procurement, finance, compliance, and human resources. The range considers a wide range of factors that are considered in making compensation decisions, including but not limited to: geographic markets, business or organizational needs, skill sets, experience, training, licensure, and certifications.

San Francisco, CA23 days ago

Remote

$264,000–$290,000 Per Year

The Payor and Health Systems Liaison leads high impact clinical, scientific, and population health engagement with external access stakeholders, including Payers, Group Purchasing Organizations (GPOs), Community Aggregators, and Integrated Delivery Networks (IDNs), while ensuring strong integration between Medical Affairs, HEOR, and Market Access strategy. They will develop and cultivate relationships with key decision-makers and other influencers in managed care organizations, government programs, employers, hospital systems and product distribution companies, to support appropriate patient access and evidence-based utilization for our client’s products.

Alameda, CA30+ days ago

$195,000–$250,000

You will oversee internal and external development partners, manage design control and technology transfer, and collaborate closely with Operations, Quality, Regulatory, and Clinical teams to ensure timely and successful program execution. The Head of Technology Development is a senior technical leader responsible for defining and executing the end‑to‑end technology strategy for Vivani’s device and drug–device combination product portfolio.

New!

South San Francisco, CA3 days ago

$200,000–$230,000 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.

South San Francisco, CA30+ days ago

$268,000–$320,000 Per Year

This role is responsible for shaping and executing customer engagement strategy across in-line products, lifecycle initiatives, and development-stage assets, with direct impact on brand performance, market understanding, and organizational alignment. The role leads a team of field-based marketers and is accountable for building a high-performing organization that delivers consistent, high-impact execution across key customer segments.

San Francisco, CA30+ days ago

Remote

MSL) at Compass Pathways is a core member of the Medical Affairs organization, connecting the company's science with the broader mental health and neuroscience community, helping to shape medical strategy, and supporting the continued development of Compass Pathways' work in treatment-resistant depression (TRD) and post-traumatic stress disorder (PTSD). The ideal candidate is passionate about a field-based role establishing themselves as a key point of scientific contact, actively engaging in high-quality scientific exchange and gathering insights from the field on emerging research, changes in the treatment landscape, and evolving approaches to care.

Fairfield, California20 days ago

$118,518.94–$154,074.63 Per Year

vendor to ensure performance and compliance, building governance structures (JOC/AOC), implementing performance monitoring frameworks and ensuring all vendors meet regulatory and . The job duties, elements, responsibilities, skills, functions, experience, educational factors and the requirements and conditions listed in this job description are representative only and not exhaustive or definitive of the tasks that an employee may be required to perform.

Martinez, CA15 days ago

$91,261–$110,929 Per Year

Four (4) years of increasingly responsible experience in a position with a housing authority or other public or assisted housing agency directly supporting daily housing operations, including two years of demonstrated experience in management of a voucher or Section 8 program another HUD-assisted housing program. Under the direction of the Director of Assisted Housing the Housing Choice Manager is responsible for the overall delivery of the Housing Authority of the County of Contra Costa’s (HACCC) high quality Housing Choice Voucher (HCV) programs within an assigned geographic area of the County of Contra Costa.

South San Francisco, CA14 days ago

$41.88–$80.90 Per Hour

The ideal candidate will collaborate cross-functionally to design and implement scalable, high-quality data solutions aligned with F.A.I.R. This role focuses on end-to-end data lifecycle management, supporting exploratory research, clinical development, and evidence generation.

South San Francisco, CA10 days ago

Remote

$280,000–$320,000 Per Year

Given the unique complexities of CAR T therapy, this role will play a critical part in addressing site-of-care dynamics, center-of-excellence (COE) networks, single case agreements, and innovative payment models to enable broad access across both academic and community oncology settings. 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.

San Francisco, CA30+ days ago

Remote

$268,000–$295,000 Per Year

Demonstrated leadership skills (proactive, strategic, creates a highly accountable team culture, provides clear direction), project management and organizational skills, with the ability to evaluate competing priorities to arrive at an appropriate decision. Oversees execution of stakeholder engagement strategy across regional and community healthcare providers, including academic institutions and community centers across the aligned region to ensure timely and accurate scientific communication.

South San Francisco, CA30+ days ago

Full-time

The MSL Director leads a team of MSLs responsible for driving clinical practice transformation in IntelliSep customer accounts, engaging with the broader clinical and medical stakeholder community supporting pre-sales discussions, and serving as internal clinical and medical subject matter experts partnering with internal teams to share HCP feedback. Reporting to the Executive Director of Medical & Scientific Affairs, the MSL Director works closely with the internal and external stakeholders to build and execute a coordinated scientific and commercial partnership strategy that enhances account development, increases clinical utilization, and drives successful and effective adoption of IntelliSep clinical workflows.

New!

South San Francisco, California2 days ago

Employee

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Regulatory Affairs Jobs in Larkspur, CA

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

Regional Director - Anesthesiology - Vituity Practice Management - Emeryville Vituity

Director of Regulatory Affairs and Policy SupplyBank.org

Associate Director, Regulatory Affairs Allogene Therapeutics

Regulatory Affairs Coordinator Public Health Foundation Enterprises, In

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

Regulatory Affairs Strategy Director Roth Staffing Companies

Snr Regulatory Affairs & Compliance Specialist PACE On Lok

VP. Regulatory Affairs Star Therapeutics

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

Vice President, Medical Affairs Vir Biotechnology

Vice President Commercial Legal Affairs Freshworks

Regulatory Intelligence Specialist The Fountain Group LLC

Senior Manager, Regulatory Operations Vir Biotechnology

Associate Regulatory Counsel, Privacy Google

Regulatory Systems Manager Ardelyx

Sr. Regulatory Documentation Control Specialist - Organic Kinder's

Regulatory Manager CEDENT

Senior Manager - Medical Affairs* Mindlance

Compliance Investigator II Partnership HealthPlan of California

Director of Quality Assurance, Clinical Caribou Biosciences, Inc.

Program Manager, NCQA San Francisco Health Plan

Director of Quality Jobot

Associate Director, Translational Science Star Therapeutics

Associate Director/Director, Clinical Science Lycia Therapeutics Inc

ASSOCIATE CNO AHMC Healthcare

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

Vice President, Clinical Development Rigel Pharmaceuticals, Inc.

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

Director, Global Medical Information & Scientific Communications Allogene Therapeutics

Senior Director, Marketing - ZILRETTA Pacira Pharmaceuticals, Inc.

Chief Risk Officer (On-site) SF Fire Credit Union

Vice President, Clinical Development (Oncology) Allogene Therapeutics

Director Biostatistics - Oncology Penfield Search Partners

Sr. Director, Biostatistics ALX Oncology Inc.

Medical Director, Pharmacovigilance Allogene Therapeutics

Compliance Program Lead Freelancer.com

Senior Director, Transactional Attorney Pacira Pharmaceuticals, Inc.

Senior Director, Payor and Health Systems Liaison Taylor Strategy Partners

Head of Technical Development Vivani Medical, Inc

Director, Attribute Sciences Allogene Therapeutics

Executive Director, Key Customer Strategy Rigel Pharmaceuticals, Inc.

(Senior) Medical Science Liaison (Pacific Northwest) Compass Pathways

Manager of Vendor Oversight Partnership HealthPlan of California

Housing Programs Manager Contra Costa Housing Authority

Clinical Data Manager II Tailored Management

Executive Director, Market Access Allogene Therapeutics

Senior Director, Regional Medical Science Liaison Taylor Strategy Partners

Director, Medical Science Liaisons Cytovale

Strategy Insights & Planning Consultant - CRM & Field Engagement ZS

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