Senior Medical Director, Clinical Development

Spyre Therapeutics

13h • $343,000 - $365,000 • Remote

About The Position

Spyre Therapeutics is a clinical-stage biotechnology company committed to developing next-generation therapies that elevate the standard in immunology by delivering more complete disease control, greater durability, and a simpler treatment experience for patients. Spyre's pipeline includes investigational extended half-life antibodies targeting α4β7, TL1A, and IL-23.

The Senior Director of Clinical Development for Rheumatology will contribute to the clinical development strategy and execution for innovative therapies targeting rheumatic indications. The Senior Director will play a pivotal role as a key clinical contributor within our global clinical development programs, partnering with cross-functional teams to support the design, planning, and implementation of study protocols and regulatory activities that advance the development of our cutting-edge antibody portfolio. This individual will join the Rheumatology Clinical Development team at a relatively early stage and will play a key role in directing research and formulating strategy to drive program success.

Requirements

• MD or equivalent medical degree is required.
• Minimum of 4+ years clinical development experience within the pharmaceutical or biotech industry within I&I indications, rheumatology strongly preferred.
• Experience with antibody therapeutics preferred.
• Proven track record in designing and executing clinical trials in immunology or inflammation.
• Experience with regulatory filings and interactions with health authorities.
• Strong understanding of GCP, clinical trial design, statistics, and global regulatory processes.
• Excellent communication and interpersonal skills, with the ability to motivate teams and collaborate effectively across functions.
• Ability to manage complex projects in a fast-paced environment.

Responsibilities

• Contribute strategic leadership and medical expertise to the clinical development of our cutting-edge antibody portfolio in rheumatic indications.
• Contribute to the study design, execution and interpretation of results, with a focus on proof-of-concept and later phases of development.
• Work closely with cross-functional teams including Biostatistics, Regulatory Affairs, and Clinical Operations to support integrated and strategic trial execution.
• Provide scientific/medical content and other input as appropriate for INDs, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other program documents. Ensure compliance with regulatory standards and guidelines, including health authority requirements for MD sign-off on patient-related matters.
• Ensure the safety of study participants by actively participating in safety monitoring and data review processes.
• Represent the Clinical Development function in interactions with regulatory agencies, investigators, KOLs, and other external stakeholders, as appropriate.
• Other activities as required.

Benefits

• Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits.
• Unlimited PTO
• Two, one-week company-wide shutdowns each
• Commitment to provide professional development opportunities.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree