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Lycia Therapeutics

Degrades extracellular proteins with LYTAC platform

Senior Manager/Associate Director Clinical Operations

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeSouth San Francisco, CA, USA$175k - $202k /yr

About the Job

Requirements

  • A BA or BS is required; an MS, PhD, PharmD, MD, or other related advanced scientific degree is strongly preferred.
  • At least 7 years of progressive advancement within clinical operations in the pharmaceutical or biotechnology industry for the manager level, or 12 years for the director level.
  • Ability to manage in a consensus environment through teamwork and trust, influence strategic direction on complex global clinical operations issues, solicit information, listen, persuade others, make important decisions, and shape outcomes.
  • Ability to work with physicians, scientists, managers, peers, and staff.

Responsibilities

  • Oversee and manage up to two early-phase clinical programs in collaboration with the selected Clinical Research Organization (CRO).
  • Create and execute clinical operational strategic plans aligned with product strategy and resource allocation.
  • Develop study feasibility assessments and cost estimates, contribute to contracts and work/change orders, and analyze tools and processes to support outsourcing efforts.
  • Track clinical program finances and monthly accruals, and review and approve associated clinical site and vendor invoices.
  • Build, develop, and train internal staff and external vendors; structure the department to enhance efficiency; and create an engaged work environment to attract and retain qualified clinical operations professionals.
  • Develop and ensure compliance with standard operating procedures, guidelines, FDA regulations, and current ICH Good Clinical Practice guidelines.
  • Oversee and maintain relationships with Contract Research Organizations, vendors, and investigative sites.
  • Participate in clinical operations and study team meetings.
  • Maintain professional expertise through familiarity with clinical literature, knowledge of the therapeutic area and current medical practice, and knowledge of pharmaceutical regulations.
  • Travel to corporate headquarters up to twice per year as needed, and travel to clinical sites or the CRO as necessary to support trial management.

Desired Qualifications

  • An MS, PhD, PharmD, MD, or other related advanced scientific degree is strongly preferred.

About the Company

Lycia Therapeutics

Degrades extracellular proteins with LYTAC platform

Lycia Therapeutics develops therapeutics using its LYTAC platform to degrade extracellular and membrane proteins involved in autoimmune and inflammatory diseases, and potentially cancer. LYTACs are bifunctional molecules where one end binds the disease protein and the other end binds a cell-surface receptor that routes the complex to the lysosome for destruction. This targets proteins outside the cell that are inaccessible to intracellular degraders like PROTACs, enabling collaborations with pharma partners to share development risk. The goal is to bring first-in-class LYTAC degraders into clinical trials, advance an autoimmune/inflammatory disease pipeline, and pursue partnerships that drive milestones and royalties.

Company size
11-50
Company stage
IPO
Headquarters
South San Francisco, CA
Founded
2020

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