Senior Director Regulatory Affairs Jobs in Delaware
Senior Director Regulatory Affairs jobs in Delaware are open across Wilmington and Newark and other Delaware metros, with employers like Incyte, Incyte Corporation, and CSC hiring at every experience level. Find a role that fits below and apply directly.
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Showing 5 of 9+ Senior Director Regulatory Affairs jobs
Overview
This position is responsible for working with the physicians within Clinical Development to provide clinical research support for programs as assigned by phase or therapeutic area.
ESSENTIAL FUNCTIONS OF THE JOB (KEY RESPONSIBILITIES)
- Maintain updated knowledge of competitive landscape in regard to assets with similar MOA and/or evolving standards of care for indications of interest.
- Serve as liaison to project teams, CRO's, Clinical sub-teams, and others.
- Clinical lead for study abstracts, posters, oral presentations, and manuscripts for assigned studies, ensuring inclusive and diverse representation in all materials.
- Develop relationships with appropriate consultants and external experts and utilize these relationships to obtain feedback on protocol design.
- Represent clinical development on project teams.
- Monitor, review and summarize safety and efficacy data in ongoing studies.
- Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans Drafting and review of clinical scientific documents such as IND, IND amendments, Investigator Brochures, Annual Reports and other Health Authority submissions.
- Development of protocols for clinical studies.
QUALIFICATIONS (MINIMAL ACCEPTABLE LEVEL OF EDUCATION, WORK EXPERIENCE, AND COMPETENCY)
- Willingness to travel up to 20% or as business needs require, with accommodations available for individuals with disabilities.
- Strong analytical skills.
- Strong written and verbal communication skills.
- Ability to work independently, manage multiple priorities, and thrive in a dynamic environment.
- Experience in oncology drug development is preferred, but not required, to encourage candidates from diverse backgrounds to apply.
- Minimum of several years of experience in research with relevant drug development experience are required. Alternative drug development experience will be considered.
- Degree in scientific/life-sciences field or equivalent experience. Advanced degrees such as Pharm.D. or Ph.D. are valued but not required.
Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
We Respect Your Privacy
Learn more at: http://www.incyte.com/privacy-policy
The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.
During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here.
You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.
You can learn more about Incyte’s data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte’s data protection officer, and your supervisory authority (if applicable).
Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.
Overview
This position is responsible for working with the physicians within Clinical Development to provide clinical research support for programs as assigned by phase or therapeutic area.
ESSENTIAL FUNCTIONS OF THE JOB (KEY RESPONSIBILITIES)
- Maintain updated knowledge of competitive landscape in regard to assets with similar MOA and/or evolving standards of care for indications of interest.
- Serve as liaison to project teams, CRO's, Clinical sub-teams, and others.
- Clinical lead for study abstracts, posters, oral presentations, and manuscripts for assigned studies, ensuring inclusive and diverse representation in all materials.
- Develop relationships with appropriate consultants and external experts and utilize these relationships to obtain feedback on protocol design.
- Represent clinical development on project teams.
- Monitor, review and summarize safety and efficacy data in ongoing studies.
- Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans Drafting and review of clinical scientific documents such as IND, IND amendments, Investigator Brochures, Annual Reports and other Health Authority submissions.
- Development of protocols for clinical studies.
QUALIFICATIONS (MINIMAL ACCEPTABLE LEVEL OF EDUCATION, WORK EXPERIENCE, AND COMPETENCY)
- Willingness to travel up to 20% or as business needs require, with accommodations available for individuals with disabilities.
- Strong analytical skills.
- Strong written and verbal communication skills.
- Ability to work independently, manage multiple priorities, and thrive in a dynamic environment.
- Experience in oncology drug development is preferred, but not required, to encourage candidates from diverse backgrounds to apply.
- Minimum of several years of experience in research with relevant drug development experience are required. Alternative drug development experience will be considered.
- Degree in scientific/life-sciences field or equivalent experience. Advanced degrees such as Pharm.D. or Ph.D. are valued but not required.
Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
We Respect Your Privacy
Learn more at: http://www.incyte.com/privacy-policy
The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.
During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here.
You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.
You can learn more about Incyte’s data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte’s data protection officer, and your supervisory authority (if applicable).
Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.
See All 9 Senior Director Regulatory Affairs Jobs in Delaware
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Find JobsSenior Director Regulatory Affairs Jobs by City in Delaware
Where Delaware roles are concentrated, by current openings.
Senior Director Regulatory Affairs Job Market in Delaware
A snapshot from current Delaware openings, updated as new roles post.
Who's Hiring
- Incyte3
- Incyte Corporation3
- CSC1
- ChristianaCare1
- Corteva Agriscience1
Top Industries Hiring
- Biotechnology & Pharmaceuticals6
- Consulting & Professional Services1
- Healthcare & Medical Services1
- Science & Research1
- Technology & Software1
What Delaware Employers Look For
The qualifications that appear most often in senior director regulatory affairs jobs across Delaware.
- Bachelor's or advanced degree in life sciences, pharmacy, chemistry, or a related field
- 10 or more years of regulatory affairs experience in pharmaceutical, biotech, or medical device sectors
- Direct experience leading FDA submissions such as NDAs, BLAs, 510(k)s, or PMAs
- Demonstrated ability to manage cross-functional teams and lead regulatory strategy across product lifecycles
- Familiarity with ICH guidelines, 21 CFR regulations, and international regulatory frameworks
- Regulatory Affairs Certification (RAC) from RAPS preferred or required by many employers
Senior Director Regulatory Affairs Jobs in Delaware: Frequently Asked Questions
How many senior director regulatory affairs jobs are there in Delaware?
There are 9+ senior director regulatory affairs openings in Delaware on Migrate Mate as of June 2026, with the most roles in Wilmington and Newark. New positions post regularly as employers across Delaware hire.
How much do senior director regulatory affairses make in Delaware?
Senior director regulatory affairses in Delaware earn a median of about $91,050 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $51,930 for the lowest 10% to over $137,540 for the top 10%. Pay rises with experience, specialty, and employer.
Which Delaware cities have the most senior director regulatory affairs jobs?
Wilmington and Newark have the most senior director regulatory affairs openings in Delaware right now, with additional roles spread across smaller metros statewide.
Which companies hire senior director regulatory affairss in Delaware?
Employers hiring senior director regulatory affairss in Delaware include Incyte, Incyte Corporation, and CSC, based on current listings on Migrate Mate as of June 2026.
Are there remote senior director regulatory affairs jobs in Delaware?
Yes. About 11% of senior director regulatory affairs openings tied to Delaware are remote or hybrid as of June 2026. The rest are on-site roles based in Delaware metros.
How do I apply for senior director regulatory affairs jobs in Delaware?
You can apply to senior director regulatory affairs jobs in Delaware directly on Migrate Mate. Search the listings above, find roles that match your experience and preferred Delaware location, then apply to each one that fits.
See All 9 Senior Director Regulatory Affairs Jobs in Delaware
Find roles in Delaware that match your experience and apply in just a few clicks.
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