ZipRecruiter

Log In

1

Clinical Research Project Assistant Jobs in Delaware

Nemours

Intern-Research PHD

Wilmington, DE · On-site

This position will assist with active research projects for 5-10 hours per week. * Must be a PhD ... clinical care, research, education, advocacy, and prevention. Our Whole Child Health approach ...

Haverford College

$43K/yr

Job Title Research Assistant Summary Haverford College invites applications for our full-time (37.5 ... Ability to adapt to evolving project needs * Ability to work effectively within a team-based ...

QPS, LLC

Research Scientist - In vitro DMPK

Newark, DE · On-site

$80K - $92K/yr

... IV Clinical Research services. To meet the needs of our clients, we strive to employ talented ... Simultaneously handle lab work as well as routine projects. * Prepare data summaries and data ...

Medi-Weightloss

Nurse Practitioner

Hockessin, DE · On-site

Our individualized treatment is supported by clinical research and translational science. License ... Physician Assistant License (Required) Salary: [Competitive, Commensurate with Experience]

previous pagenext page

Showing results 21-40

All JobsClinical Research Project JobsClinical Research Project Assistant JobsClinical Research Project Assistant Jobs in Delaware

Clinical Research Project Assistant information

See Delaware salary details

$8

$22

$46

How much do clinical research project assistant jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical research project assistant in Delaware is $22.73, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What is the difference between Clinical Research Project Assistant vs Clinical Research Coordinator?

AspectClinical Research Project AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCR are common
Work EnvironmentSupports research teams in clinical settings, hospitals, or research institutionsManages daily clinical trial activities, interacts directly with patients and investigators
Employer & Industry UsageUsed by research institutions, hospitals, pharmaceutical companiesCommonly employed in clinical trial sites, hospitals, and research organizations

The Clinical Research Project Assistant primarily supports research activities and data management, while the Clinical Research Coordinator oversees trial operations and patient interactions. Both roles require similar educational backgrounds and certifications, but their responsibilities differ in scope and daily tasks.

What are the most commonly searched types of Clinical Research Project jobs in Delaware? The most popular types of Clinical Research Project jobs in Delaware are:
What are popular job titles related to Clinical Research Project Assistant jobs in Delaware? For Clinical Research Project Assistant jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Clinical Research Project Assistant jobs in Delaware look for? The top searched job categories for Clinical Research Project Assistant jobs in Delaware are:
What cities in Delaware are hiring for Clinical Research Project Assistant jobs? Cities in Delaware with the most Clinical Research Project Assistant job openings:
Clinical Research Project Assistant jobs near you

Associate Director, Clinical R&D QA US

Incyte Corporation

Wilmington, DE • On-site

$35.50 - $47.25/hr

Full-time

Posted 24 days ago

Job description

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.
SUMMARY
This position is responsible for providing GCP oversight of Clinical development teams to the Head of Incyte Global R&D QA. This role will also include the execution and management of Incyte QA GCP audits and the provision of GCP guidance and advice across assigned Clinical Development programs.
The Senior Manager Clinical R&D QA is also the QA lead for clinical inspection activities related to the clinical programs under its quality oversight.
DUTIES AND RESPONSABILITIES
  • Provide QA GCP advice and support to Incyte Clinical Development/Operations functions and other relevant functions as assigned.
  • Plan, schedule and conduct audits of Clinical Investigator Sites, Vendors, , Trial Master Files and Clinical submission documents.
  • Assist with the management of QA consultants performing audits on behalf of Incyte QA.
  • Lead regulatory authority inspections activities for development programs assigned including conducting pre-inspection audits, inspection readiness activities and coordination/hosting inspection role, as assigned.
  • Coordinate responses and corrective/preventative actions from deviations, audit and regulatory findings.
  • Assist with the maintenance of the clinical Quality Management System including QA support for change control, deviations, review/revision of SOPs with ensuring continuous process improvement
  • Stay abreast of clinical trial requirements, ICH GCP, and guidelines from other regulatory agencies for the management of clinical trials as appropriate.
  • Alert Global Clinical R&D QA Upper Management of internal and external GCP compliance and clinical trial issues in a timely manner.
  • Mentoring Junior Clinical QA as assigned
  • Promote Quality Culture with external R&D stakeholders, as assigned
  • Stay abreast of local/country clinical activities/initiatives from Regional Clinical Operations members and ensure necessary QA oversight in place as Clinical R&D QA Point of contact.
  • Conduct GCP training for Incyte staff.
  • Be knowledgeable and be able to understand advanced operational, scientific and/or clinical research areas.
  • Be thoroughly familiar with assigned Incyte Compounds and protocol

REQUIREMENTS
  • Bachelor's degree in a science or healthcare related discipline, or similarly conferred degree from a university
  • 5 to 7 years' experience in a pharmaceutical or bio-pharmaceutical company in a GCP QA role or Clinical compliance role.
  • Minimum of 5 years' experience performing GCP audits of investigator sites and/or CROs
  • English fluency written and spoken (the company language)
  • Regulatory inspection experience as coordinator or key role
  • Ability to travel up to 30%.
  • Excellent written and oral communication skills.
  • This role is office-based.

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.

Apply