Director Clinical Development

Description:

Kennedy Bond, in partnership with a global leader in rare disease innovation, is seeking a highly skilled Director of Clinical Development to play a pivotal role in advancing transformative therapies for patients with rare conditions. This organization is dedicated to addressing critical unmet medical needs by developing life-changing treatments through cutting-edge science and clinical excellence.

As the Director of Clinical Development, you will be responsible for leading and overseeing the planning, execution, and management of Phase I–III clinical trials across rare disease programs. The role involves close collaboration with cross-functional teams including regulatory affairs, medical affairs, and commercial divisions to ensure alignment of clinical strategies with overall business objectives. You will engage with key opinion leaders, investigators, patient advocacy groups, and regulatory authorities, ensuring robust scientific and clinical strategies.

A core aspect of this role includes monitoring emerging scientific advancements and competitive trends to guide clinical development strategies. Additionally, you will provide leadership and mentorship to team members, fostering a high-performing and accountable clinical operations function.

Key Responsibilities:

• Lead the end-to-end planning and execution of rare disease clinical trials (Phase I–III).

• Collaborate with cross-functional teams to integrate clinical strategies with business goals.

• Build and maintain strong relationships with investigators, KOLs, patient advocacy groups, and regulators.

• Stay informed on evolving scientific and competitive landscapes to optimize clinical programs.

• Mentor, guide, and develop clinical development teams to enhance operational excellence.

Candidate Requirements:

• MD or equivalent clinical/scientific degree.

• 7–10 years of experience in clinical development, with a strong preference for rare disease programs.

• Proven track record of successfully managing clinical trials from protocol design through to regulatory submission.

• Strong leadership, communication, and collaboration skills with cross-functional teams.

• A genuine passion for improving outcomes and advancing treatment options for patients with rare diseases.