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Alector

Biopharmaceutical R&D for neurodegenerative therapies

Vice President - Clinical Development

Clinical Research OperationsUpdated on Nov 10
Full-timeUnited StatesNo salary listed

About the Job

Requirements

  • A Ph.D. in Neuroscience, Neurobiology, or an equivalent field is required; an M.D. is preferred.
  • At least 10 years of experience leading clinical development in the biotechnology or pharmaceutical industry, including experience taking programs through early clinical development.
  • Extensive clinical expertise in the management and execution of Alzheimer disease and related neurodegenerative disease programs.
  • Drug development experience in neurodegenerative disease.
  • Strong knowledge of clinical trial design, medical monitoring, clinical data interpretation, benefit-risk assessment, and regulatory requirements supporting clinical drug development.
  • Experience designing and executing first-in-human and Phase 1 and 2 studies, including dose escalation and interpretation of early safety, pharmacokinetic, pharmacodynamic, and biomarker data.
  • Experience working with regulators and contributing clinical content to regulatory submissions and interactions.
  • Ability to exercise independent medical judgment and provide clinical leadership within cross-functional development teams, including serving as the primary internal clinical expert for a program.
  • Ability to translate complex scientific and clinical information into clear recommendations and collaborate with scientists, development colleagues, executives, investigators, and external experts.
  • Active use of large language models and strong interest in evolving AI technologies and their application to improve drug development quality, speed, and efficiency.
  • Experience working in a small or rapidly evolving biotechnology organization where clinical leaders combine strategic thinking with hands-on execution.

Responsibilities

  • Lead the clinical development strategy for AL137, owning the clinical and medical strategy for Phase 1 and helping shape the program's path toward later-stage development by integrating emerging clinical, translational, safety, and biomarker data into clear decisions.
  • Provide medical leadership for Phase 1 protocol design and execution, eligibility and safety considerations, dose escalation, clinical data review, and interpretation of emerging results in partnership with Clinical Operations and investigators.
  • Serve as the internal physician expert for AL137 and provide clinical perspectives to program teams and senior leadership.
  • Build productive relationships with investigators, external experts, partners, and regulatory authorities as appropriate.
  • Partner across Biometrics, Translational Medicine, Safety, Regulatory, and other functions to define the evidence needed for critical development decisions and communicate the clinical meaning of emerging data.
  • Identify practical ways to use AI and emerging technologies to accelerate analysis, improve decision-making, streamline clinical-development work, and conserve time and resources.

About the Company

Alector

Biopharmaceutical R&D for neurodegenerative therapies

Alector is a biopharmaceutical company that develops therapies for neurodegenerative diseases such as Alzheimer's and Parkinson's. It uses insights from immunology, neurology, and human genetics to create medicines that help the body heal itself. The company focuses on researching and developing novel therapeutic candidates, mainly through early-stage clinical trials to quickly gather disease-specific data and improve the chances of success. Revenue and funding come from partnerships, grants, and eventual product commercialization. Alector aims to advance treatments for unmet medical needs in neurodegenerative diseases by pursuing a pipeline that combines scientific findings with strategic drug development.

Company size
51-200
Company stage
IPO
Headquarters
San Francisco, CA
Founded
2013

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