Remote Clinical Development Scientist Immunology/IBD

Spyre Therapeutics

United States

Remote

USD 175,000 - 205,000

Full time

3 days ago
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Benefits offered by this job

Unlimited PTO
Company-wide shutdowns
Remote work with occasional in-person
Professional development opportunities

Job summary

Spyre Therapeutics is seeking a Clinical Scientist, Clinical Development to design, execute, and interpret clinical trials for their antibody therapies. The role requires collaboration across clinical operations, regulatory, translational science, and biomarker teams to ensure robust study designs and high-quality data.

You will help drive program progression while maintaining regulatory compliance and scientific integrity.

Qualifications

  • 5+ years of clinical development experience in biotech/pharma.
  • Experience in immunology or immune-mediated diseases.
  • Bachelor's degree in life sciences; advanced degree is a plus.
  • Familiarity with FDA/ICH, GCP.

Responsibilities

  • Collaborate with clinical operations, data management and CRO to ensure patient safety and protocol compliance.
  • Regularly review clinical trial data, including adverse events and lab data.
  • Assist in Medical Monitor responsibilities.
  • Contribute to study design and amendments with stakeholders.
  • Author regulatory documents and review protocols and amendments.
  • Support trial execution with site selection, start-up, monitoring and quality oversight.
  • Prepare and review abstracts, posters and presentations for scientific meetings.

Skills

Cross-functional collaboration
Regulatory knowledge
Scientific writing
Study design
Data interpretation

Education

Bachelor's degree in life sciences or related

Job description

Spyre Therapeutics is seeking a Clinical Scientist, Clinical Development to design, execute, and interpret clinical trials for their antibody therapies. The role requires collaboration across clinical operations, regulatory, translational science, and biomarker teams to ensure robust study designs and high-quality data.

You will help drive program progression while maintaining regulatory compliance and scientific integrity.

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