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Director Laboratory Operations Jobs in Delaware (NOW HIRING)

Operations Technician (TCP)

Millsboro, DE · On-site

$48K - $76K/yr

Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers ... laboratory services in various manufacturing areas. Throughout your career, we will offer you ...

Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers ... Planning and implementing daily and weekly laboratory assignments as well as special projects and ...

Showing results 41-60

Director Laboratory Operations information

See Delaware salary details

$34K

$107.8K

$179.7K

How much do director laboratory operations jobs pay per year?

As of Sep 4, 2026, the average yearly pay for director laboratory operations in Delaware is $107,773.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,600.00 and $135,600.00 per year, depending on experience, location, and employer.

What is a director laboratory operations?

A Director of Laboratory Operations oversees the daily functions, strategic planning, and overall efficiency of a laboratory. They are responsible for ensuring compliance with regulations, managing budgets, and coordinating staff to maintain high-quality standards. This role often involves optimizing workflows, implementing new technologies, and collaborating with leadership to support research or clinical objectives. Strong leadership, problem-solving, and laboratory management experience are essential for success in this position.

What are the typical career advancement opportunities for someone in a director laboratory operations role?

A Director Laboratory Operations can pursue advancement to executive roles such as Vice President of Laboratory Services, Chief Operating Officer, or even Chief Scientific Officer, depending on the organization’s structure. This role provides valuable leadership experience and exposure to high-level strategy, budgeting, and cross-departmental collaboration. Many directors also expand their expertise by leading larger teams, overseeing multiple laboratory sites, or participating in organizational growth initiatives. Continued professional development and success in this position often open doors to significant influence on company direction and industry innovation.

What are the key skills and qualifications needed to thrive in the director laboratory operations position, and why are they important?

To excel as a Director Laboratory Operations, you need strong leadership abilities, extensive experience in laboratory management, and an advanced degree in a scientific or technical field. Familiarity with laboratory information management systems (LIMS), regulatory compliance standards (such as CLIA, CAP, or ISO), and safety protocols is crucial. Excellent communication, strategic thinking, and problem-solving skills distinguish top performers in this role. These competencies ensure efficient laboratory operations, regulatory adherence, and effective team leadership in a complex and fast-paced environment.

What are the most commonly searched types of Laboratory Operations jobs in Delaware?

The most popular types of Laboratory Operations jobs in Delaware are:

What are popular job titles related to Director Laboratory Operations jobs in Delaware?

For Director Laboratory Operations jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Director Laboratory Operations jobs in Delaware look for?

The top searched job categories for Director Laboratory Operations jobs in Delaware are:

Infographic showing various Director Laboratory Operations job openings in Delaware as of August 2026, with employment types broken down into 83% Full Time, 14% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $107,773 per year, or $51.8 per hour.

Senior Director - Executive Director, Hematology Oncology Drug Development

Incyte Corporation

Wilmington, DE • On-site

Full-time

Posted 23 days ago


Key responsibilities

  • Provides guidance for the implementation and accomplishment of investigator-initiated trials related to product development and life cycle management of a compound.

  • Collaborates with external vendors and regulatory bodies to facilitate clinical studies and ensure compliance with regulatory standards.

  • Develops and facilitates the creation of key documents such as clinical study protocols, informed consents, CSRs, and scientific publications related to product development.


Job description

Overview
Overview
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity. Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
Job Summary
The Senior Director - Executive Medical Director, Drug Development is responsible for implementing clinical drug efforts for Incyte's oncology products (Phase I though Phase III).
Essential Functions of the Job
  • Provides guidance for successful implementation and accomplishment of investigator-initiated trials related to product development and life cycle management of a compound.
  • Implements the highest ethical and regulatory standards during the investigation and development of anticancer agents.
  • Works in partnership with medical affairs for successful launch of future antineoplastic agents.
  • Detects and analyzes emergent issues during clinical drug development and develops and implements mitigating strategies.
  • Represents Incyte Corporation at key national and international medical and scientific meetings including participation in advisory boards with key opinion leaders.
  • Liaises with discovery science to facilitate and further the development of investigational agents from a preclinical stage to clinical development.
  • Serves as a source for medical and scientific expertise in oncology for outlining design strategy and execution for anti-cancer drug development.
  • Collaborates with external vendors such as CROs, external imaging and laboratory resources, as well as global pharmaceutical companies for successful implementation and conduct of early phase and registration global clinical studies.
  • 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.
  • Interacts with global regulatory bodies including the FDA and EMA to accomplish tasks related to oncology product development and collaborates with internal regulatory experts and oversee the clinical research plans and sections for Investigational new Drug applications (INDs) and New Drug Applications (NDAs).
  • Provides medical and scientific expertise for internal cross-functional team members for development of specific anti-neoplastic agents including discovery scientists, medical scientists, biostatisticians, pharmacokineticists, pharmacovigilance and clinical operations.

Qualifications (Minimal acceptable level of education, work experience, and competency)
  • M.D. or D.O. degree with a minimum of 3-5 years of experience in oncology drug development in a biotechnology or pharmaceutical company.
  • Board certified or eligible in Oncology preferred.
  • Ability to multi-task and work in a dynamic environment.
  • Excellent written and verbal communication skills.

Please Note: Candidates with a range of oncology drug development experience are encouraged to apply. The final title and level (Senior Director or Executive Director) will be determined by the hiring team based on relevant experience, scientific expertise, leadership potential, and overall fit for the role.
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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.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
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.