Director, Global Regulatory CMC

Benefits

Parental leave

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Non-birth-parent leave

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Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

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Relocation assistance

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Childcare support

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Learning budget

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Verification

Not verified checked Jun 13, 2026

Salary

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401(k) match

Reported from DOL Form 5500 industry filing (not employer-specific)

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Market context

U.S. role benchmark (BLS OEWS)

$61,842 U.S. median for this role

Projected growth (BLS Employment Projections)

+1.9% - Slower

Matched to SOC 11-1021 - Operations aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Schedule

Shift type

Not verified

Weekend work

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Company

Company stage

Public-company Verified - from the job posting source checked Jun 20, 2026

Application

Cover letter

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Assessment

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Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Director, Global Regulatory CMC US_North Carolina_Remote COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. JOB SUMMARY: The Director, Global Regulatory CMC will work closely with project teams and CMC Leadership in setting and meeting company goals as they relate to CMC matters. This position will be responsible for ensuring efficient and productive strategic and operational regulatory CMC support for BioCryst development programs. The position will work to develop and implement key new values and added initiatives focused on the coordination of the company's regulatory CMC program with the Clinical, Nonclinical, Regulatory, and QA groups. This position will be responsible for development and implementation of a Global Regulatory CMC plan, addressing research and product development needs, as well as the integration of the global regulatory strategic plan into the research, and product developmental missions. ESSENTIAL DUTIES & RESPONSIBILITIES: Manages all global regulatory

Read the full description at biocryst.wd501.myworkdayjobs.com. FewerJobs shows a preview and links to the original posting.