Project Manager, IND Development

AmpersandPeople

  • San Diego, CA
  • 5 days ago

    Highlights

    Built by a dynamic team of serial entrepreneurs, expert scientists, and drug developers, we are advancing bispecific ADCs engineered to target receptor co-complexes that are highly expressed on certain solid tumors with enhanced tumor cell specificity and internalization. The Senior Project Manager must have substantial experience managing the intersection of complex programs across multiple domain-based biotech teams (e.g., Toxicology, Pharmacology, Bioanalytical, CMC, Regulatory Affairs, and Quality Control).

    Numbers & Facts

    LocationSan Diego, CA

    Description

    Overview:

    The Senior Project Manager will support the advancement of Sidewinder Therapeutics' antibody-drug conjugate (ADC) pipeline by driving cross-functional project planning and execution from discovery through IND submission. This role is crucial in enabling Sidewinder Therapeutics’ first-in-human clinical trials. The Senior Project Manager must have substantial experience managing the intersection of complex programs across multiple domain-based biotech teams (e.g., Toxicology, Pharmacology, Bioanalytical, CMC, Regulatory Affairs, and Quality Control). The ideal candidate approaches unfamiliar technical areas with high curiosity. They prioritize credibility and co-elevation to organize and advance their colleagues' technical expertise and to evolve the organization's broader priorities.


    Key Responsibilities:

    • Provide leadership and proactive mitigation by maintaining and communicating program risk registers, decision logs, and cross-functional action items.
    • Lead cross-functional core team meetings that maintain alignment across workstreams and shared milestones.
    • Own integrated development timelines connecting all drug development teams as well as external CRO/CDMO partners (e.g., nonclinical/toxicology, bioanalytical method development, regulatory submissions, etc.)
    • Possess exceptional organizational and communication skills to track and elevate cross-team dependencies and risks specific to ADC development.
    • Support preparation and coordination of IND-enabling documents, regulatory submissions, governance meetings, and program reviews.
    • Track project metrics, maintain project documentation, and ensure activities are conducted in accordance with company processes and regulatory expectations.
    • Extend project management support to additional company priorities and programs by applying the same rigorous, collaborative coordination to company decision-making.


    Qualifications:

    • Bachelor's degree in a scientific discipline; advanced degree or PMP certification preferred.
    • 7+ years of project management experience within biotechnology or pharmaceutical development, including experience supporting IND-enabling programs.
    • Working knowledge of CMC development for ADCs, biologics, and/or small molecules (e.g., conjugation chemistry, analytical characterization, drug product formulation).
    • Familiarity with GLP toxicology study design and nonclinical development timelines.
    • Experience managing cross-functional drug development teams (i.e., internally and CROs/CDMOs) with a track record of successful IND submissions.
    • Experience with GxP environments, 21 CFR, pre-IND meeting processes, and life sciences regulatory requirements preferred.
    • Strong understanding of FDA regulations, ICH guidelines, and pharmaceutical development processes.
    • Experience with navigating the complexities of bispecific antibody and novel payload development is preferred.
    • Familiarity with biologic, small molecule, and combined regulatory considerations is a strong plus.
    • Excellent organizational, communication, and stakeholder management skills, with strong attention to detail and problem-solving abilities.
    • Demonstrated ability to build effective working relationships across technical domains.
    • A track record of proactively learning new technical or therapeutic areas.


    Salary & Benefits:

    Sidewinder Therapeutics is committed to providing employees with market-competitive compensation and an excellent benefits program, including Medical, Dental, and Vision plans, company-paid holidays, and more!


    About Sidewinder Therapeutics:

    Sidewinder Therapeutics is pioneering the next generation of bispecific antibody-drug conjugates.

    We aim to deliver next-generation bispecific antibody-drug conjugates (ADCs) that expand the therapeutic window for patients with difficult-to-treat cancers. Built by a dynamic team of serial entrepreneurs, expert scientists, and drug developers, we are advancing bispecific ADCs engineered to target receptor co-complexes that are highly expressed on certain solid tumors with enhanced tumor cell specificity and internalization.

    Perks:

    • Sidewinder Therapeutics is committed to providing employees with market-competitive compensation and an excellent benefits program, including Medical, Dental, and Vision plans, company-paid holidays, and more!

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