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Evommune

Develops tissue-based therapies for inflammation

Director, Clinical Operations

Clinical Research OperationsUpdated on Nov 11
Full-timePalo Alto, CA, USA

About the Job

Requirements

  • A bachelor's degree or higher in life sciences is required.
  • At least 7 years of clinical operations leadership experience and 10 years in the pharmaceutical or biotechnology industry, or a relevant clinical research organization, are required.
  • Demonstrated experience leading study execution in a start-up or small biotechnology environment is required.
  • A strong understanding of regulatory, technical, scientific, and operational knowledge related to drug development is required.
  • Experience operating in a clinical-stage or resource-disciplined biotechnology environment is required.
  • Strategic thinking with a strong execution focus is required.
  • Comfort operating in a lean, fast-paced environment is required.
  • Strong project management and organizational skills are required.
  • A high-accountability and ownership mindset is required.
  • Strong written and verbal communication skills are required.
  • The ability to influence cross-functionally without direct authority is required.

Responsibilities

  • Lead and oversee execution of one or more clinical trials according to program timelines and budgets, proactively mitigating risks related to trial conduct, deliverables, vendor performance, and quality.
  • Select and oversee contract research organizations and ancillary vendors, and serve as the primary escalation point for execution issues or risks related to deliverables.
  • Interact with and establish relationships with key clinical trial investigators.
  • Contribute to clinical development strategy for one or more programs, providing input on the design and operationalization of the clinical development plan.
  • Develop and finalize protocols and clinical study reports in collaboration with Clinical Development, ensuring scientific and operational accuracy.
  • Lead or oversee writing, review, and approval of key clinical project deliverables, including clinical study protocols, scope definition documents, investigational product labeling and kitting, pharmacy manuals, informed consent documents, institutional review board and ethics committee submissions and approvals, site activations, monitoring plans and tools, case report forms, data management plans, safety plans, close-out plans, and inspection readiness plans.
  • Provide input to clinical sections of regulatory documents, including Investigator Brochures, DSURs, and IND annual reports.
  • Provide operational expertise to internal functions, including CMC, regulatory affairs, nonclinical, medical writing, and biometrics, and to external teams, including contract research organizations and consultants, to ensure study goals are met.
  • Report program progress, risks, issues, and metrics to executive leadership as needed.
  • Develop and ensure compliance with company standard operating procedures and guidelines, FDA regulations, and current ICH GCP guidelines.
  • Hire and manage additional Clinical Operations staff based on program resource needs.
  • Provide financial information related to clinical development and interface with the finance group to manage trial costs.
  • Travel as required to ensure successful trial execution.

Desired Qualifications

  • Experience in drug development for inflammatory, dermatologic, or pain/CNS indications is preferred.

About the Company

Evommune

Develops tissue-based therapies for inflammation

Evommune develops therapies for chronic inflammatory diseases. It uses human tissue to study the immune system and uncover pathways to medicines, helping identify and advance drug candidates efficiently. The company collaborates with other top teams across target discovery, pre-IND, and clinical development, and generates revenue by developing and commercializing its therapies for patients and healthcare providers. Compared with competitors, Evommune relies on tissue-based insights from human biology to guide drug selection and prioritization, reducing risk and speeding development, all through a partnership-driven model. Its goal is to improve patient outcomes and quality of life by delivering safer, more effective treatments for chronic inflammatory diseases.

Company size
51-200
Company stage
IPO
Headquarters
Palo Alto, CA
Founded
2020

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