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Clinical Research Associate Sponsor Dedicated Jobs in Delaware

Agilent

Clinical Affairs Scientist

Wilmington, DE · On-site +1

$105K - $197K/yr

The candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance ...

New

CEDENT

Study Start-Up Manager

Wilmington, DE

Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up milestones. * Participate in Local Study Team meetings and report on site performance metrics. * Ensure ...

AstraZeneca

CRA Manager - Cell Therapy

Wilmington, DE · On-site

As CRA Manager within US Site Management and Monitoring, you will direct a group of Clinical Research Associates to deliver robust site performance, first-time quality, and on-time execution across a ...

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All JobsClinical Research Associate Sponsor Dedicated JobsClinical Research Associate Sponsor Dedicated Jobs in Delaware

Clinical Research Associate Sponsor Dedicated information

What is a clinical research associate sponsor dedicated?

A Clinical Research Associate (CRA) Sponsor Dedicated is a professional who monitors clinical trials on behalf of a pharmaceutical or biotechnology company (the sponsor), rather than working for a contract research organization (CRO). Their primary responsibility is to ensure that clinical studies are conducted in compliance with protocols, regulations, and good clinical practice (GCP) guidelines. They act as a liaison between the sponsor and research sites, overseeing data accuracy, patient safety, and regulatory documentation. Being sponsor dedicated means they work exclusively for one sponsor, allowing for deeper familiarity with that company’s processes and studies.

How does a clinical research associate sponsor dedicated typically interact with clinical sites and sponsor teams during a study?

As a Clinical Research Associate (Sponsor Dedicated), you will serve as a crucial liaison between the sponsor and clinical sites. Your responsibilities include monitoring site compliance, ensuring data integrity, and providing training or support to site staff. You will regularly communicate with both the sponsor’s project team and site personnel to address issues, resolve queries, and facilitate smooth trial operations. This role often involves travel to clinical sites, frequent status updates with sponsor representatives, and participation in team meetings to discuss study progress and challenges.

What are the key skills and qualifications needed to thrive as a clinical research associate sponsor dedicated, and why are they important?

To thrive as a Clinical Research Associate Sponsor Dedicated, a solid understanding of clinical trial processes, Good Clinical Practice (GCP), and a relevant life sciences degree are essential. Familiarity with electronic data capture (EDC) systems, regulatory compliance software, and often a GCP certification are typically required. Strong organizational skills, attention to detail, and effective communication help ensure smooth collaboration between sponsors, sites, and regulatory bodies. These skills are vital for maintaining data integrity, regulatory compliance, and the successful execution of clinical trials.

What is the difference between Clinical Research Associate Sponsor Dedicated vs Clinical Research Associate?

AspectClinical Research Associate Sponsor DedicatedClinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRA or RAC are commonSame as Sponsor Dedicated, often with similar certifications and educational background
Work EnvironmentWorks closely with sponsor teams, often in dedicated clinical trial units or officesWorks across multiple sites, monitoring clinical trials in various locations
Employer & Industry UsageEmployed by sponsors or CROs with a focus on specific sponsor trialsEmployed by CROs, pharmaceutical companies, or biotech firms, overseeing multiple trials

Both roles require similar qualifications and certifications, but the Clinical Research Associate Sponsor Dedicated primarily works within a sponsor's dedicated team, focusing on specific trials, while the Clinical Research Associate generally monitors multiple sites across various trials.

What are popular job titles related to Clinical Research Associate Sponsor Dedicated jobs in Delaware?

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

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

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

What cities in Delaware are hiring for Clinical Research Associate Sponsor Dedicated jobs?

Cities in Delaware with the most Clinical Research Associate Sponsor Dedicated job openings:

Clinical Research Associate Sponsor Dedicated jobs near you
Infographic showing various Clinical Research Associate Sponsor Dedicated job openings in Delaware as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 16% Part Time, and 8% Contract. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution.

Senior Director Clinical Research Scientist

Incyte Corporation

Wilmington, DE • On-site

Full-time

Re-posted 28 days ago

Job description

Overview
Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health care, and build sustainable value.
The Company strives to discover and develop first-in-class and best-in-class medicines-advancing a diverse portfolio of large and small molecules.
Position Overview
We are seeking a Clinical Scientist to join our Early Clinical Development Group at a level commensurate with experience (Associate Director through Executive Director).
This role is intentionally designed to attract both emerging leaders and experienced strategic contributors. Depending on level, you will contribute to or lead early clinical development and clinical pharmacology programs, with increasing ownership, strategic influence, and cross-functional leadership at more senior levels. You will have the opportunity to work across the full product lifecycle-from First-in-Human studies through approval and post-marketing-within a collaborative, science-driven environment that values curiosity, innovation, and continuous learning.
Key Responsibilities:
Core Responsibilities (All Levels)
  • Contribute to the design, execution, and interpretation of early clinical and clinical pharmacology studies
  • Collaborate cross-functionally with Clinical Operations, Translational Sciences, Quantitative Clinical Pharmacology, and Statistics
  • Support development of clinical documents including protocols, study reports, and regulatory submissions
  • Analyze and interpret clinical safety and efficacy data in collaboration with Medical and Scientific teams
  • Maintain awareness of competitive landscape and emerging standards of care
  • Ensure adherence to timelines, budgets, SOPs, and regulatory requirements
  • Present data internally and contribute to external scientific communications

Additional Responsibilities by Level
Associate Director
  • Lead components of clinical studies and contribute to program-level strategy
  • Draft and independently own sections of key clinical and regulatory documents
  • Collaborate closely with cross-functional partners to execute study deliverables
  • Present findings to internal teams

Director / Senior Director
  • Lead clinical studies and drive cross-functional execution
  • Contribute meaningfully to clinical development strategy
  • Serve as a scientific leader on project teams and influence decision-making
  • Mentor junior team members and contribute to team development

Executive Director
  • Provide strategic leadership across programs or therapeutic areas
  • Shape and drive clinical development strategy and represent programs to governance bodies
  • Influence portfolio-level decisions and external collaborations
  • Serve as a recognized subject matter expert internally and externally
  • Lead high-visibility initiatives, including regulatory interactions and scientific presentations

Qualifications
Minimum Requirements
  • PhD, PharmD, or MD with 5+ years of relevant experience, OR
  • BS/MS with 10+ years of relevant experience
  • Experience in early clinical development, clinical pharmacology, or a related discipline
  • Strong analytical, communication, and problem-solving skills
  • Ability to work independently and collaboratively in a dynamic environment

Additional Experience by Level
Associate Director
  • Experience contributing to clinical studies and cross-functional teams
  • Demonstrated ability to analyze and interpret clinical data

Director / Senior Director
  • Proven experience leading clinical studies or key program components
  • Ability to influence cross-functional teams and contribute to strategy

Executive Director
  • Extensive experience leading clinical development programs
  • Strong track record of strategic leadership and influencing senior stakeholders
  • Experience representing programs in high-visibility settings (e.g., regulatory interactions, governance)

Preferred Qualifications (All Levels)
  • Experience in clinical pharmacology, immunology, or oncology
  • Strong scientific curiosity and a proactive, question-driven mindset
  • Ability to present complex data clearly and effectively

Additional Information
Willingness to travel up to 20% as needed (reasonable accommodations available)
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.
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