Full-time · On-site

Director, Clinical Operations

This is a high-level leadership opportunity to head the clinical operations of a biotech firm specializing in previously undruggable GPCR targets. The role offers a unique blend of strategic oversight and hands-on execution, perfect for someone who wants to build a department while staying close to the science. With a significant salary and high organizational visibility, it is a premier role for an experienced clinical professional.

S
Hiring company

Septerna

South San Francisco, California, United States · Posted 29 April 2026

The role

Overview

This is a high-level leadership opportunity to head the clinical operations of a biotech firm specializing in previously undruggable GPCR targets. The role offers a unique blend of strategic oversight and hands-on execution, perfect for someone who wants to build a department while staying close to the science. With a significant salary and high organizational visibility, it is a premier role for an experienced clinical professional.

The hiring side

About Septerna

Septerna is a small business working in biotechnology, based in South San Francisco, California, United States.

Industry

Biotechnology

Size

Small

Location

South San Francisco, California, United States

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What they need

Requirements & Skills

Key Responsibilities

  • Lead the strategic planning and execution of global clinical programs across multiple therapeutic areas
  • Ensure all clinical trials meet rigorous quality, regulatory, and safety standards
  • Manage clinical trial budgets and resource allocation effectively
  • Collaborate with senior leadership to align clinical operations with corporate development goals
  • Drive continuous improvement in clinical trial methodologies and operational efficiency

Essential

  • Proven leadership in operational planning for clinical programs
  • Experience managing Phase I through Phase III global clinical trials
  • Ability to oversee end-to-end delivery of patient-facing studies
  • Expertise in maintaining compliance with regulatory and quality standards
  • Track record of delivering trials on time and within budget

Preferred

  • Experience in a fast-growing biotech or startup environment
  • Familiarity with GPCR-focused drug discovery or small molecule programs
  • Strong background in cross-functional team leadership

Key Skills

Strategic clinical planningBudget managementRegulatory compliance (GCP/ICH)Cross-functional collaborationOperational excellenceProject managementCreative problem-solving

Networking

People to Know

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Perks

Benefits & perks

  • Competitive annual salary ($225k - $250k)
  • Opportunity to work on ground-breaking GPCR technology
  • High visibility with senior leadership
  • Collaborative and inclusive work environment
  • Professional growth and development opportunities
  • Participation in a mission-driven biotech culture

Next step

Apply now

Found via xtalks.com

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