Full-Time

Regulatory Affairs Senior Associate/Manager

Updated on 9/3/2026

Dispatch Biotherapeutics

Dispatch Biotherapeutics

51-200 employees

Cloud-based software linking labs and providers

No salary listed

San Francisco, CA, USA + 1 more

More locations: Philadelphia, PA, USA

Hybrid

The role may be onsite or hybrid.

Bachelor's, Master's, PharmD, PhD

Category
Biology & Biotech (1)

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Requirements
  • Bachelor’s degree in life sciences or a related discipline.
  • A minimum of 2 years of Regulatory Affairs experience within the biotechnology or pharmaceutical industry for Senior Associate level.
  • A minimum of 5 years of Regulatory Affairs experience within the bio/pharma industry for Manager level.
  • Direct experience supporting oncology drug development, including investigational new drug application-stage programs.
  • Ability to independently drive projects while knowing when to escalate or seek alignment.
  • Hands-on experience authoring and managing regulatory submissions and health authority correspondence.
  • Strong understanding of Food and Drug Administration regulations and International Council for Harmonisation guidelines relevant to clinical-stage development.
  • Ability to work onsite or in a hybrid setup.
  • Excellent written and verbal communication skills, with strong attention to detail.
  • Highly organized, with the ability to manage multiple priorities in a fast-moving environment.
  • Collaborative, proactive, and comfortable operating in a small, resource-constrained startup setting.
Responsibilities
  • Author, review, and manage technically complex regulatory submissions, including investigational new drug applications, amendments, meeting briefing packages, annual reports, and responses to health authority questions for the DISP-10 program in solid tumors.
  • Serve as a regulatory core team member on study teams, providing guidance to cross-functional stakeholders on regulatory requirements and risks.
  • Support health authority interactions, including preparation for and participation in meetings and other health authority interactions with agencies such as the Food and Drug Administration and the Therapeutic Goods Administration.
  • Manage regulatory operations activities, including preparing document submissions, submission planning, and maintenance of regulatory archives.
  • Contribute to and execute global regulatory strategies for the lead asset from early development through clinical stages.
  • Track, assess, and communicate relevant regulatory intelligence, guidance, and policy trends impacting oncology and cell therapy development.
  • Support interactions with external partners, including contract research organizations and regulatory vendors, ensuring alignment with regulatory strategy and timelines.
  • Ensure regulatory activities comply with applicable regulations, guidelines, and internal processes.
  • Contribute to continuous improvement of regulatory processes, tools, and templates appropriate for a growing organization.
Desired Qualifications
  • Advanced degree, such as a Master of Science, Doctor of Philosophy, or Doctor of Pharmacy.
  • Prior experience with cell therapy or advanced therapy medicinal products.
  • Experience working in early-stage or startup biotechnology environments.
  • Direct experience supporting solid tumor drug development.
  • Direct experience preparing original investigational new drug application submissions.
  • Exposure to global regulatory development, such as work with the European Medicines Agency or other ex-U.S. agencies.
  • Experience supporting regulatory aspects of chemistry, manufacturing, and controls and manufacturing activities for cell therapies.
Dispatch Biotherapeutics

Dispatch Biotherapeutics

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Dispatch Bio provides a cloud-based software platform for infectious disease diagnostics. It connects patients, providers, and laboratories to deliver faster, more accurate test results. The core product is a SaaS system that laboratories use to manage test orders, workflows, and results reporting, while healthcare providers use it to order tests and receive timely results for patients. The platform integrates the entire diagnostic process in a single system, reducing turnaround times and streamlining communication across the care team. Compared with typical lab software, Dispatch Bio focuses on end-to-end workflow integration, strong data security and regulatory compliance, and a B2B model that targets diagnostic labs and healthcare providers. Its goal is to modernize diagnostic testing to enable quicker diagnoses and better patient management in infectious diseases.

Company Size

51-200

Company Stage

Series A

Total Funding

$216M

Headquarters

Philadelphia, Pennsylvania

Founded

2022

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Simplify Jobs

Simplify's Take

What believers are saying

  • August 6, 2026 first-patient dosing de-risks execution and strengthens investor credibility.
  • Fast Track designation accelerates FDA engagement and potential 2027 efficacy readouts.
  • August 2026 CARsgen collaboration expands Flare into China with zevor-cel.

What critics are saying

  • DISP-10 depends on viral delivery, CAR-T trafficking, and antigen stability; one failure kills efficacy.
  • Single-platform concentration leaves Dispatch exposed if 2026 safety signals derail Flare.
  • No commercial revenue makes a failed Phase 1 an existential capital trap before 2028.

What makes Dispatch Biotherapeutics unique

  • Dispatch pairs tumor-specific virus DV-10 with CAR-T, creating a programmable antigen platform.
  • Carl June, ARCH, PICI, and BMS anchor Dispatch's 2025-2026 solid-tumor strategy.
  • August 2026 first-patient dosing validates Dispatch's clinic-ready manufacturing and trial engine.

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Benefits

Health Insurance

Vision Insurance

Dental Insurance

Life Insurance

Unlimited Paid Time Off

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

0%

2 year growth

0%
Business Wire
Apr 27th, 2026
Dispatch Bio's SEND T cell armoring strategy shows 200X+ therapeutic window in solid tumors

Dispatch Bio presented preclinical data on its SEND T cell armoring strategy at the American Society of Gene & Cell Therapy 2026 Annual Meeting in Boston. The technology uses a synthetic cytokine receptor to simultaneously activate multiple pathways for optimal T cell function, designed to overcome limitations in the tumour microenvironment. Preclinical results showed SEND-armoured CAR T cells achieved tumour clearance at low doses with a therapeutic window exceeding 200-fold. The treatment demonstrated efficacy with or without lymphodepleting chemotherapy. Single-cell RNA sequencing revealed simultaneous enrichment of effector and memory gene programmes within individual cells, indicating robust expansion without exhaustion. Dispatch Bio believes SEND could apply broadly across engineered T cell approaches, including autologous CAR T therapies and TCR-based treatments. The company's Flare platform combines immunotherapy with tumour-specific virus engineering for solid tumour treatment.

BioSpace
Nov 5th, 2025
Dispatch Bio Unveils First Clinical Program and Presents Data Supporting Flare Platform at Society for Immunotherapy of Cancer (SITC) 2025 Annual Meeting

Dispatch Bio unveils first clinical program and presents data supporting Flare platform at Society for Immunotherapy of Cancer (SITC) 2025 Annual Meeting. November 5, 2025 | Encouraging preclinical data validate Dispatch's scientific approach and support advancement of DISP-10 toward clinical development in 2026 PHILADELPHIA & SAN FRANCISCO-(BUSINESS WIRE)-Dispatch Bio, a biotechnology company developing a universal treatment for solid tumors, today announced preclinical data supporting its first therapeutic program planned to enter the clinic, DISP-10, and its first-in-class Flare platform, at the Society for Immunotherapy of Cancer (SITC) 2025 Annual Meeting. Immunotherapies have had limited success in solid tumors due to the lack of tumor-specific targets and a profoundly immunosuppressive microenvironment. Dispatch's Flare platform addresses these barriers by systemically delivering a tumor-specific virus that paints a universal synthetic antigen (Flare) on tumor cells, enabling precise recognition by T cells, while reshaping the tumor microenvironment to support immune activity. Data presented at SITC (Abstract 394) demonstrate strong and consistent tumor labeling, iterative viral amplification and tumor cell clearance across multiple epithelial tumor models. "These data show that delivering engineered targets specifically to tumor cells allows us to control antigen specificity, while also reprogramming the tumor microenvironment," said Lex Johnson, Ph.D., Co-Founder and Chief Platform Officer. "We are excited to start with CAR T as our first program, and because the Flare approach is modular and not restricted to CAR T cells, it can be extended across multiple immunotherapy modalities." The company also presented preclinical findings from DISP-10, its first therapeutic candidate (Abstract 393). DISP-10 pairs DV-10, a tumor-targeted virus expressing a modified BCMA antigen (dBCMA) and the immune-stimulatory cytokine IL-18 and chemokine CXCL9, with a clinically validated BCMA-directed CAR T. The viral component installs the target and drives local immune activation, enabling robust CAR T function in solid tumors. DISP-10 demonstrated potent anti-tumor responses in numerous in vitro and in vivo models, with no activity observed in healthy cells. Dispatch plans to initiate a first-in-human Phase 1 study in 2026 to evaluate DISP-10 across multiple solid tumor types. "DISP-10 creates the right biological context for CAR T cells to function in solid tumors," said Barbra Sasu, Ph.D., Chief Scientific Officer. "The consistency of activity seen with various BCMA-targeted therapies across tumor models gives us confidence in its clinical potential." Dispatch also announced a clinical supply and collaboration agreement with Bristol Myers Squibb (BMS). Under the agreement, BMS will supply idecabtagene vicleucel (ide-cel) as the CAR T-cell component for Dispatch's first U.S. Phase 1 trial of DISP-10. DV-10, emerging from the Flare platform, provides the tumor-specific targeting and immune activation necessary for CAR T-cell function in solid tumors. Please see full Prescribing Information for idecabtagene vicleucel (ide-cel), including Boxed WARNINGS and Medication Guide. About Dispatch Bio Established in 2022, Dispatch Bio was founded with a bold purpose: to help create a world where all cancer patients can be cured. To achieve this, the company is engineering a universal treatment across solid tumors, leveraging its first-in-class Flare platform. This novel approach combines the strengths of immunotherapy with a tumor-specific virus, both engineered to clear tumor cells with precision and power. Dispatch has operations in Philadelphia and San Francisco, with access to world-class researchers. To learn more, visit www.dispatchbio.com and follow us on LinkedIn and X.

Fierce Biotech
Jul 23rd, 2025
Cancer biotech Dispatch unveils with $216M and CAR-T pioneer Carl June as cofounder

Dispatch Bio has unveiled with $216 million and the lofty goal of creating a universal treatment for solid tumors using a new immunotherapy approach. | Dispatch Bio has unveiled with $216 million and the lofty goal of creating a universal treatment for solid tumors using a new immunotherapy approach.