Senior Director, Clinical Development - US - Remote

Overview

Join a leading life sciences organization committed to advancing treatments for serious diseases. This senior leadership role offers the opportunity to shape innovative clinical development strategies, influence global regulatory pathways, and collaborate with cross-functional teams driving transformative therapies. You will have the chance to make a meaningful impact on patients’ lives while enjoying a dynamic, supportive environment that fosters growth and leadership.

About our client

Our client is a pioneering organization in the biotech and pharmaceutical sector, dedicated to developing therapies that improve patient outcomes. Their mission is to push the boundaries of science, bringing innovative solutions from discovery through clinical development. This company values leadership, scientific excellence, and collaborative problem-solving to help address unmet medical needs worldwide.

The opportunity (Role summary)

As a Senior Director of Clinical Development, you will spearhead clinical strategy and oversee the execution of late-stage programs for molecules transitioning from discovery. You will act as a key leader, working closely with research teams, external partners, and regulatory bodies to ensure the delivery of high-quality clinical data. Based on-site, you will be integral to shaping the company’s pipeline and ensuring compliance with global standards. This role offers the chance to influence the future of drug development and advance breakthrough therapies for patients.

Key responsibilities

• Lead clinical input for the planning and development of late-stage molecules, ensuring alignment with global regulatory standards.
• Oversee clinical execution, manage development timelines, and coordinate with external partners and cross-functional teams.
• Support translational and regulatory activities, including preparing submissions to authorities and maintaining awareness of evolving standards.
• Serve on transition teams to guide molecules in-licensed, acquired, or partnered, ensuring seamless integration into development pipelines.
• Drive continuous improvement in clinical trial design, execution, and data interpretation to support global Phase 1–2a programs.
• Maintain up-to-date knowledge of emerging science, competitive landscapes, and global standards across relevant disease areas.

What you’ll bring

• Proven experience in clinical development leadership, including overseeing global Phase 1–2a clinical programs.
• Deep understanding of regulatory pathways in regions including the US, Europe, and Japan.
• Experience with NDA, MAA, and J-NDA submissions, especially in innovative therapies.
• Strong leadership and cross-functional collaboration skills.
• Ability to work effectively in a fast-paced environment and adapt to evolving scientific and regulatory landscapes.
• Advanced degree in life sciences or a related field.

Compensation & benefits

This role offers a competitive salary in the range of $300,000–$350,000, depending on experience. Compensation details will be shared during the process.

Our client provides comprehensive benefits, including medical, dental, and vision coverage, generous paid time off, flexible work arrangements, and a robust investment in employee development and growth. You will have opportunities for leadership development, cross-functional collaboration, and contributing to impactful projects that can shape the future of medicine.

Call to action

Ready to lead innovative clinical programs and make a significant impact in the biotech space? Apply now to join a forward-thinking organization dedicated to transforming patient care and advancing science.

Human review note: This description has been crafted to highlight why this role is a unique opportunity, focusing on impact, growth, and collaborative leadership. No proprietary or specific company information has been included, ensuring confidentiality and compliance with client requirements.