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Clinical Research Jobs in Delaware (NOW HIRING)

Healthcare Degree

Clinical Trials Manager

Newark, DE · On-site

$125 - $150/hr

Clinical trial managers are responsible for coordinating and overseeing the entire clinical research process, ensuring that studies are conducted safely, ethically, and in compliance with regulatory ...

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Clinical Research information

See Delaware salary details

$49K

$107.4K

$189.2K

How much do clinical research jobs pay per year?

As of Sep 8, 2026, the average yearly pay for clinical research in Delaware is $107,429.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,100.00 and $122,600.00 per year, depending on experience, location, and employer.

What is clinical research?

Clinical research is a branch of healthcare science that focuses on studying human health and illness through clinical trials and observational studies. It aims to improve medical knowledge by testing new treatments, drugs, medical devices, or interventions in controlled environments. Clinical research professionals design, conduct, and monitor studies to ensure that data is accurate and that participant safety and ethical standards are maintained. The results of clinical research can lead to new therapies, improved patient care, and informed healthcare policies.

What are different clinical research jobs?

Some of the different types of clinical research jobs include clinical research associates, coordinators, data managers, clinical nurses, research scientists, and biostatisticians. There are also administrative, managerial, and recruitment positions. As a research associate, you monitor the clinical trials and the people administering them, such as clinical nurses and research coordinators who work under the direction of the principal investigator. As a biostatistician, your duties are to collect data about the study and analyze the results to determine if the medication or treatment shows statistically significant effects on participants.

What are the key skills and qualifications needed to thrive in clinical research, and why are they important?

To thrive in Clinical Research, you need a strong background in life sciences, data analysis, and regulatory compliance, often supported by a relevant degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are commonly required. Attention to detail, strong organizational skills, and effective communication make candidates stand out in this field. These skills ensure the integrity of research data, regulatory adherence, and successful collaboration among cross-functional teams.

What are some typical challenges faced by professionals in clinical research, and how can they be managed?

Clinical research professionals often face challenges such as strict regulatory compliance, tight timelines, and coordination among multidisciplinary teams. Managing large volumes of data and ensuring participant safety are also key concerns. Staying organized, maintaining open communication with team members, and keeping updated on regulatory changes can help professionals navigate these challenges effectively. It's also helpful to develop strong project management skills and to build collaborative relationships with investigators, sponsors, and regulatory bodies.

What is the difference between Clinical Research vs Clinical Data Coordinator?

AspectClinical ResearchClinical Data Coordinator
Required CredentialsTypically a bachelor's degree in health sciences, life sciences, or related field; certifications like CCR or CCRA are commonOften a bachelor's degree in health or data management; certifications like CDMP or CCRC may be preferred
Work EnvironmentResearch sites, pharmaceutical companies, CROs, hospitalsClinical trial sites, hospitals, research organizations
Job FocusDesigning, managing, and overseeing clinical trialsManaging and ensuring accuracy of clinical trial data

Clinical Research involves overseeing entire clinical trials, including protocol development and compliance, while Clinical Data Coordinators focus on collecting, managing, and ensuring the quality of trial data. Both roles are essential in the clinical research process but differ in scope and responsibilities.

How do you become a clinical researcher?

To become a clinical researcher, typically a bachelor's degree in a health-related field such as biology, nursing, or medicine is required, followed by relevant experience or advanced education like a master's or PhD. Certification in clinical research, such as the Certified Clinical Research Professional (CCRP), can enhance job prospects. Strong analytical skills, knowledge of regulatory guidelines, and familiarity with research tools are also important.

Is clinical research a good career path?

Clinical research is a viable career that involves managing and conducting trials to test new medical treatments and drugs. It requires strong organizational skills, knowledge of regulatory guidelines, and often a background in healthcare or life sciences. The field offers opportunities for advancement and specialization, with roles in research coordination, data management, and regulatory affairs.

What do you do in a clinical research job?

A clinical research job involves designing, conducting, and managing studies to evaluate the safety and effectiveness of medical treatments or devices. Professionals in this field collect and analyze data, ensure compliance with regulatory standards, and often work with clinical trial participants, using tools like electronic data capture systems. Strong attention to detail, knowledge of Good Clinical Practice (GCP), and relevant certifications are important for success.

What qualifications do you need to be a clinical research professional?

A clinical research professional typically needs a bachelor's degree in a health-related field such as biology, nursing, or pharmacy. Relevant certifications, like the Certified Clinical Research Professional (CCRP), and knowledge of Good Clinical Practice (GCP) guidelines are often required. Strong organizational skills and familiarity with clinical trial management systems are also important.
More about Clinical Research jobs

What are the most commonly searched types of Clinical Research jobs in Delaware?

The most popular types of Clinical Research jobs in Delaware are:

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For Clinical Research jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Clinical Research jobs in Delaware look for?

The top searched job categories for Clinical Research jobs in Delaware are:

What cities in Delaware are hiring for Clinical Research jobs?

Cities in Delaware with the most Clinical Research job openings:

Clinical Research jobs near you
Infographic showing various Clinical Research job openings in Delaware as of August 2026, with employment types broken down into 3% As Needed, 87% Full Time, 5% Part Time, and 5% Contract. Highlights an 85% In-person, 3% Hybrid, and 12% Remote job distribution, with an average salary of $107,429 per year, or $51.6 per hour.

Senior Director Clinical Research Scientist

Incyte Corporation

Wilmington, DE • On-site

Full-time

This job post has expired 4 days ago. Applications are no longer accepted.

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
As a Senior Director Clinical Scientist within Early Clinical Development, you will play a central role in the design, execution, and interpretation of early-phase clinical studies for innovative programs across Incyte's expanding portfolio.
You will operate at the interface of science and strategy, shaping development plans that translate molecular innovation into clinical value. Working in partnership with physicians, discovery scientists, and cross-functional experts, you will influence key decisions that determine the trajectory of our investigational assets.
This position offers the opportunity to work on first-in-class and best-in-class compounds, driving programs that represent the future of Incyte's pipeline and the next wave of progress for patients worldwide.
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:
  • 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
  • Degree in scientific/life-sciences field or equivalent experience. Advanced degrees such as Pharm.D. or Ph.D. are valued but not required.
  • Minimum of several years of experience in research with relevant drug development experience are required. Alternative drug development experience will be considered.
  • Experience in oncology drug development is preferred, but not required, to encourage candidates from diverse backgrounds to apply.
  • 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.

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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