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Director Post Production Jobs in Delaware (NOW HIRING)

AWSPRODVK1

Product Manager

Townsend, DE · On-site

$12K - $13K/yr

Demonstrated ability to lead cross-functional teams and influence without direct authority ... and post-launch analysis. * Conduct market research and competitive analysis to identify ...

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All JobsPost Production JobsDirector Post Production JobsDirector Post Production Jobs in Delaware

Director Post Production information

See Delaware salary details

$24K

$107.6K

$189.7K

How much do director post production jobs pay per year?

As of Aug 21, 2026, the average yearly pay for director post production in Delaware is $107,570.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,100.00 and $129,600.00 per year, depending on experience, location, and employer.

What is a director post production?

A Director of Post Production is a senior professional responsible for overseeing the entire post-production process in film, television, or digital media projects. This role manages editing, sound design, visual effects, color correction, and final delivery, ensuring the creative vision is realized within budget and deadlines. They coordinate teams of editors, sound engineers, and other specialists, while liaising with producers and directors to maintain quality and consistency. The Director of Post Production also helps solve technical or creative challenges that arise after filming is complete.

What are the key skills and qualifications needed to thrive as a director post production?

To thrive as a Director of Post Production, you need extensive experience in video editing, project management, and a deep understanding of post-production workflows, typically backed by a relevant degree and years in the industry. Mastery of software like Avid Media Composer, Adobe Premiere Pro, DaVinci Resolve, and knowledge of color grading and audio post systems are standard requirements. Outstanding leadership, communication, and problem-solving skills set apart top candidates in managing teams and navigating tight deadlines. These skills ensure the seamless delivery of high-quality content and efficient oversight of complex post-production processes.

What are some common challenges faced by a director post production, and how can they be managed effectively?

A Director of Post Production often navigates challenges such as tight deadlines, balancing creative vision with budget constraints, and coordinating large, multidisciplinary teams. Effective management involves clear communication among editors, sound designers, visual effects artists, and producers to ensure everyone is aligned on project goals. Leveraging project management tools and maintaining flexible workflows can help address unexpected issues, while fostering a collaborative environment supports both creativity and efficiency. Taking the initiative to stay updated on the latest post-production technologies also enables smoother operations and high-quality results.

What is the difference between Director Post Production vs Post Production Supervisor?

AspectDirector Post ProductionPost Production Supervisor
ResponsibilitiesOversees entire post production process, manages creative vision, coordinates departmentsManages daily operations, schedules, and workflow within post production
CredentialsExperience in editing, editing software, industry knowledgeExperience in post production, technical skills, project management
Work EnvironmentCreative teams, editing suites, production officesPost production facilities, editing suites, production offices
Industry UsageFilm, TV, digital mediaFilm, TV, digital media

The main difference is that the Director Post Production focuses on the creative and overall vision of the project, while the Post Production Supervisor handles the day-to-day technical and operational aspects to ensure timely delivery.

What are the most commonly searched types of Post Production jobs in Delaware?

The most popular types of Post Production jobs in Delaware are:

What job categories do people searching Director Post Production jobs in Delaware look for?

The top searched job categories for Director Post Production jobs in Delaware are:

What cities in Delaware are hiring for Director Post Production jobs?

Cities in Delaware with the most Director Post Production job openings:

Director Post Production jobs near you
Infographic showing various Director Post Production job openings in Delaware as of August 2026, with employment types broken down into 82% Full Time, 13% Part Time, 3% Contract, and 2% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $107,570 per year, or $51.7 per hour.

Senior/ Executive Medical Director, Medical Lead IAI, Early Clinical Development

Incyte Corporation

Wilmington, DE • On-site

Full-time

Re-posted 3 days ago

Job description

Overview
Incyte is a global, science-driven biopharmaceutical company recognized for its strong growth and deep commitment to advancing therapies in Hematology, Oncology, and Immunology.
With a diverse and expanding early pipeline, Incyte is shaping the next generation of targeted and immune-based therapies. Our strength lies in our ability to combine scientific insight with clinical execution, transforming discoveries into impactful medicines for patients worldwide.
We are a company in motion, growing, evolving, and investing in early development as a core engine of innovation. At Incyte, every idea begins with science - and every scientist plays a part in shaping what comes next.
The role:
This position is responsible for implementing early clinical development efforts for Incyte's Dermatology, Immunology, Rheumatology products (preclinical candidate nomination through transition to registrational studies)
Duties and Responsibilities
  • Leads development efforts for assets post-candidate selection through first in human trials, including early dose escalation, ph 1-2a translational strategy (proof of mechanism studies) and proof of concept studies in human (ph 1b or 2a).
  • Participates in asset/portfolio strategies and prioritization, internal and external messaging, governance, and cross-functional interface with all key stakeholders, including translational science, clinical pharmacology and pharmacometrics, discovery organization, regulatory and others.
  • Provides medical and scientific expertise for internal cross-functional team members for development of specific, dermatology and immunology agents including discovery scientists, clinical scientists, biostatisticians, pharmacokinetics, pharmacovigilance, and clinical operations.
  • Supports interactions with global regulatory bodies including the FDA, EMA, PMDA and TGA and ethics committees to accomplish tasks related to product development and collaborates with internal regulatory experts and oversee the clinical research plans and sections for Investigational new Drug applications (INDs) and other regulatory documents.
  • Facilitates the development of key internal and external documents pertaining to product development including clinical study protocol, informed consents, CRFs, CSRs, meeting abstracts, scientific journal publications, strategy documents and project plans.
  • Collaborates with external vendors such as CROs, external imaging and laboratory vendors for successful implementation and conduct of early phase clinical studies.
  • Represents Incyte Corporation at key national and international medical and scientific meetings including participation in advisory boards with key opinion leaders.
  • Detects and analyzes emergent issues during early clinical drug development and develops and implements mitigating strategies.
  • Works in partnership with medical affairs and commercial organization for successful launch of future agents.
  • Implements the highest ethical and regulatory standards during the investigation and development of anticancer agents.
  • Provides guidance for successful implementation and accomplishment of investigator-initiated trials related to product development and life cycle management of a compound.
  • Acts as subject matter expert for business development activities

Requirements
  • MD, MD-PhD (or PhD with > 8-year clinical development experience in immunology or dermatology). For MDs a dermatology, rheumatology or clinical immunology/ allergy board certification is preferred.
  • Training in research (wet lab), proven track record of self-directed scientific work (e.g. post doc, peer reviewed publications as first author) preferred. Experience in early drug development required with proven track record of leading clinical pre-clinical candidate to PoC in human
  • Proficient in English, oral and written. Member of at least one professional society (e.g. SID, ACR, AAAAI). Strives for continued medical education in immunology related area.
  • Ability to lead sub-teams and drive projects
  • Track record of business development and due diligence team support
  • Proven record of successful work in diverse, cross-functional teams (co located or not). Willingness to share and coach other Incyte employees within ED and beyond.
  • Desirable preferred behaviour: active listening, higher than average social sensitivity, empathy, willingness to mentor and coach.

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.
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