Clinical Research Assistant Jobs in Delaware
Clinical Research Assistant jobs in Delaware are concentrated in Wilmington, Newark, and the greater New Castle County corridor, where AstraZeneca, Christiana Care Health System, and Nemours Children's Health anchor a dense clinical and pharmaceutical research ecosystem. Demand is strongest in oncology trials, cardiovascular research, and pediatric studies, reflecting the specialties of Delaware's largest research institutions. Openings appear at every level from entry-level coordinator roles to senior research assistant positions managing multi-site protocols. See the openings below and apply to the ones that match your experience.
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Nemours is seeking a Clinical Research Nurse to join our team in Wilmington, DE.
The Division of Critical Care at Nemours Children’s Hospital Delaware is seeking a Clinical Research Nurse (CRN) to support, expand, and lead the clinical research program within the pediatric intensive care unit (PICU). Applicants should be motivated to work with families, children, and staff in a highly collaborative environment focused on outstanding clinical care, education, and research. The CRC/CRN will join a productive research team that is overseen by a Research Manager and the Director of Research for the PICU.
Candidates should have familiarity and experience with human subjects’ research regulations, though additional professional development in this area will also be provided. Prior experience working in health care or clinical research is required. Additional required skills include ability to work with children, experience with computer data entry and management, and familiarity with common computer programs, such as Microsoft Word and Excel and Adobe. CRCs and CRNs in Critical Care are also expected to pursue, and will be supported in their pursuit, of career advancement opportunities.
The PICU at Nemours embraces a multi-professional, multi-specialty collaborative care model that is patient- and family-centered. As one of the nation's premier pediatric health care systems, Nemours is committed to do whatever it takes to prevent and treat even the most disabling childhood conditions. It's a promise that extends beyond our nationally recognized clinical treatment to an entire integrated spectrum of research, advocacy, education, and prevention.
Essential Functions:
1. Follows all aspects of Standard Operating Procedures and Good Clinical Practices in the conduct of clinical research; collects and prepares documents as required by sponsoring agencies; attends Investigator Meetings, as assigned
2. Understands and can conduct clinical research studies that require but not limited to Emergent Access/Compassionate use, Multi-site clinical trials, conduct Investigator Initiated studies, Research Team training manuals
3. Participates in the conduct of parental permission/assent process for assigned studies; schedules study visits with study participants in accordance with study protocols; develops strategies to assure compliance of study participants with protocol requirements.
4. Performs clinical data gathering, measurements and monitoring of data integrity, including data completeness, accuracy and quality. Maintains multiple study databases. Ability to be submit data proactively and address queries in a timely manner.
5. Participates in training nursing and ancillary study staff for study purposes; builds relationships with various departments to ensure protocol compliance.
6. Assists in identifying, reporting and following up on Serious Adverse Events and/or Unanticipated problems
7. Assists in the maintenance of study medication accountability records; works closely with research pharmacist to coordinate study drug administration and documentation
8. Prepares clinical specimens for shipment to central laboratories. Ensures manual of procedures is followed and applicable documentation is sent with samples
9. Coordinates monitoring activities with Sponsor’s representative(s). Completes Case Report Forms; responds to sponsor queries, prepares for audits by sponsor, IRB and/or the FDA/DHHS.
10. Participates in continuous process improvement initiatives and implementation of outcomes
11. Prepares for internal and external audits. Prepares corrective action plans as indicated.
Requirements:
ASN Required, BSN preferred. Associate degree in Nursing will require obtaining BSN within 3 years of hire date.
Active Delaware Nursing License
Clinical Research Coordinator certification or eligible to sit for exam after 2 years clinical research coordination experience
1 year of Clinical Research experience required
Basic Life Support Certification
#LI-RR1
Nemours is seeking a Clinical Research Nurse to join our team in Wilmington, DE.
The Division of Critical Care at Nemours Children’s Hospital Delaware is seeking a Clinical Research Nurse (CRN) to support, expand, and lead the clinical research program within the pediatric intensive care unit (PICU). Applicants should be motivated to work with families, children, and staff in a highly collaborative environment focused on outstanding clinical care, education, and research. The CRC/CRN will join a productive research team that is overseen by a Research Manager and the Director of Research for the PICU.
Candidates should have familiarity and experience with human subjects’ research regulations, though additional professional development in this area will also be provided. Prior experience working in health care or clinical research is required. Additional required skills include ability to work with children, experience with computer data entry and management, and familiarity with common computer programs, such as Microsoft Word and Excel and Adobe. CRCs and CRNs in Critical Care are also expected to pursue, and will be supported in their pursuit, of career advancement opportunities.
The PICU at Nemours embraces a multi-professional, multi-specialty collaborative care model that is patient- and family-centered. As one of the nation's premier pediatric health care systems, Nemours is committed to do whatever it takes to prevent and treat even the most disabling childhood conditions. It's a promise that extends beyond our nationally recognized clinical treatment to an entire integrated spectrum of research, advocacy, education, and prevention.
Essential Functions:
1. Follows all aspects of Standard Operating Procedures and Good Clinical Practices in the conduct of clinical research; collects and prepares documents as required by sponsoring agencies; attends Investigator Meetings, as assigned
2. Understands and can conduct clinical research studies that require but not limited to Emergent Access/Compassionate use, Multi-site clinical trials, conduct Investigator Initiated studies, Research Team training manuals
3. Participates in the conduct of parental permission/assent process for assigned studies; schedules study visits with study participants in accordance with study protocols; develops strategies to assure compliance of study participants with protocol requirements.
4. Performs clinical data gathering, measurements and monitoring of data integrity, including data completeness, accuracy and quality. Maintains multiple study databases. Ability to be submit data proactively and address queries in a timely manner.
5. Participates in training nursing and ancillary study staff for study purposes; builds relationships with various departments to ensure protocol compliance.
6. Assists in identifying, reporting and following up on Serious Adverse Events and/or Unanticipated problems
7. Assists in the maintenance of study medication accountability records; works closely with research pharmacist to coordinate study drug administration and documentation
8. Prepares clinical specimens for shipment to central laboratories. Ensures manual of procedures is followed and applicable documentation is sent with samples
9. Coordinates monitoring activities with Sponsor’s representative(s). Completes Case Report Forms; responds to sponsor queries, prepares for audits by sponsor, IRB and/or the FDA/DHHS.
10. Participates in continuous process improvement initiatives and implementation of outcomes
11. Prepares for internal and external audits. Prepares corrective action plans as indicated.
Requirements:
ASN Required, BSN preferred. Associate degree in Nursing will require obtaining BSN within 3 years of hire date.
Active Delaware Nursing License
Clinical Research Coordinator certification or eligible to sit for exam after 2 years clinical research coordination experience
1 year of Clinical Research experience required
Basic Life Support Certification
#LI-RR1
See All 8 Clinical Research Assistant Jobs in Delaware
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Find JobsClinical Research Assistant Jobs by City in Delaware
Where Delaware roles are concentrated, by current openings.
Clinical Research Assistant Job Market in Delaware
A snapshot from current Delaware openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Healthcare & Medical Services
- Biotechnology & Pharmaceuticals
What Delaware Employers Look For
The qualifications that appear most often in clinical research assistant jobs across Delaware.
- Bachelor's degree in a life sciences, biology, or health-related field required
- Experience with clinical trial protocols, GCP guidelines, and regulatory documentation
- Proficiency in electronic data capture systems such as REDCap or Medidata Rave
- Strong attention to detail for maintaining accurate case report forms and source documents
- Ability to obtain and maintain CITI Program certification in human subjects research
- Excellent organizational skills to coordinate participant scheduling and study visits
Clinical Research Assistant Jobs in Delaware: Frequently Asked Questions
How do you become a clinical research assistant in Delaware?
A bachelor's degree in biology, public health, nursing, or a related life science is the standard entry point for clinical research assistant roles in Delaware. Delaware does not require a state-issued license specific to clinical research, but employers across Wilmington and Newark strongly prefer candidates who hold or are working toward CITI Program certification in Good Clinical Practice. Many roles at Delaware's pharmaceutical and hospital employers also expect familiarity with FDA regulations governing clinical trials.
Which companies hire clinical research assistants in Delaware?
Companies currently hiring clinical research assistants in Delaware include Nemours Children's Health, AstraZeneca, and Incyte Corporation, per current listings on Migrate Mate as of November 2026. Delaware's concentration of major pharmaceutical headquarters and academic medical centers makes it one of the more active markets for clinical research hiring on the East Coast.
Which Delaware cities have the most clinical research assistant jobs?
Wilmington, Newark, and Middletown account for the largest share of clinical research assistant openings in Delaware. Wilmington leads because of the pharmaceutical and biotech companies headquartered there, while Newark benefits from its proximity to the University of Delaware and Christiana Care's main campus, and smaller suburban markets see consistent openings tied to satellite research sites and specialty clinics.
Are there remote clinical research assistant jobs in Delaware?
Yes, but they're rare. Clinical research assistant work is largely hands-on, requiring direct patient contact, site visits, and in-person protocol oversight that can't be done remotely. About 0% of clinical research assistant openings tied to Delaware are remote or hybrid as of November 2026, and those positions typically involve data entry, regulatory document management, or monitoring coordination rather than direct study participation.
How can I get hired as a clinical research assistant in Delaware with little or no experience?
The most realistic entry path is applying for clinical research coordinator trainee or research associate roles at Christiana Care Health System or Nemours Children's Health, both of which periodically hire candidates directly from degree programs and provide structured onboarding in GCP and trial operations. Lateral moves from phlebotomy, medical assisting, or EMT roles are common at Delaware's hospital-based research programs. Completing CITI Program certification before applying gives entry-level candidates a concrete credential that distinguishes them from other new applicants.
Where can I find and apply to clinical research assistant jobs in Delaware?
You can find and apply to clinical research assistant jobs in Delaware on Migrate Mate, which lists current Delaware openings. Search the available roles, find the ones that match your background and target location, and apply directly to the positions that fit.
See All 8 Clinical Research Assistant Jobs in Delaware
Find roles in Delaware that match your experience and apply in just a few clicks.
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