The Director of Clinical Research will manage a team of data analysts', system engineers, biostatisticians, and Research Scientists within the Research Institute as well as within the context of the ...
Posted today
The Director of Clinical Research will manage a team of data analysts', system engineers, biostatisticians, and Research Scientists within the Research Institute as well as within the context of the ...
Posted today
The Director of Clinical Research will manage a team of data analysts', system engineers, biostatisticians, and Research Scientists within the Research Institute as well as within the context of the ...
Posted today
Wilmington, DE · On-site
$23.50 - $31.25/hr
The Clinical Research Coordinator coordinates, implements and completes clinical research studies and/or clinical trials in the Orthogenetics Department at Nemours Children's Hospital Delaware by ...
Wilmington, DE · On-site
$23.50 - $31.25/hr
The Clinical Research Coordinator coordinates, implements and completes clinical research studies and/or clinical trials in the Orthogenetics Department at Nemours Children's Hospital Delaware by ...
$23.50 - $31.25/hr
The Clinical Research Coordinator II coordinates, implements and completes clinical research studies and/or clinical trials in the Orthopedics Department at Nemours Children's Hospital Delaware by ...
$23.50 - $31.25/hr
The Clinical Research Coordinator II coordinates, implements and completes clinical research studies and/or clinical trials in the Orthopedics Department at Nemours Children's Hospital Delaware by ...
Wilmington, DE · On-site
$23.50 - $31.25/hr
The Clinical Research Coordinator II coordinates, implements and completes clinical research studies and/or clinical trials in the Orthopedics Department at Nemours Children's Hospital Delaware by ...
Wilmington, DE · On-site
$23.50 - $31.25/hr
The Clinical Research Coordinator II coordinates, implements and completes clinical research studies and/or clinical trials in the Orthopedics Department at Nemours Children's Hospital Delaware by ...
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 ...
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 ...
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 ...
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 ...
The Clinical Research Technologist II serves as a bench technologist for the laboratories in the ... This position is also responsible for providing progress and update reports to the lab manager and ...
The Clinical Research Technologist II serves as a bench technologist for the laboratories in the ... This position is also responsible for providing progress and update reports to the lab manager and ...
The Clinical Research Technologist II serves as a bench technologist for the laboratories in the ... This position is also responsible for providing progress and update reports to the lab manager and ...
The Clinical Research Technologist II serves as a bench technologist for the laboratories in the ... This position is also responsible for providing progress and update reports to the lab manager and ...
Wilmington, DE · On-site
The incumbent supervises and coordinates the responsibilities of research nurses and staff conducting studies and oversees the management of all clinical research projects conducted at Nemours ...
Wilmington, DE · On-site
The incumbent supervises and coordinates the responsibilities of research nurses and staff conducting studies and oversees the management of all clinical research projects conducted at Nemours ...
Wilmington, DE · On-site
The incumbent supervises and coordinates the responsibilities of research nurses and staff conducting studies and oversees the management of all clinical research projects conducted at Nemours ...
Wilmington, DE · On-site
The incumbent supervises and coordinates the responsibilities of research nurses and staff conducting studies and oversees the management of all clinical research projects conducted at Nemours ...
... Clinical Research Technologist II The Clinical Research Technologist II serves as a bench ... This individual will work under the supervision of the Biobank Laboratory Manager and perform ...
Posted today
... Clinical Research Technologist II The Clinical Research Technologist II serves as a bench ... This individual will work under the supervision of the Biobank Laboratory Manager and perform ...
Posted today
Management reserves the right to change or modify such duties as required. We Respect Your Privacy Learn more at: The Incyte hiring organization processes your personal data to manage your job ...
Management reserves the right to change or modify such duties as required. We Respect Your Privacy Learn more at: The Incyte hiring organization processes your personal data to manage your job ...
Incyte is committed to the rigorous pursuit of research and development excellence to improve the ... Management reserves the right to change or modify such duties as required. Incyte Corporation is ...
Incyte is committed to the rigorous pursuit of research and development excellence to improve the ... Management reserves the right to change or modify such duties as required. Incyte Corporation is ...
Job Summary The clinical scientist will provide scientific clinical and operational input to early ... Management reserves the right to change or modify such duties as required. Incyte Corporation is ...
Job Summary The clinical scientist will provide scientific clinical and operational input to early ... Management reserves the right to change or modify such duties as required. Incyte Corporation is ...
Wilmington, DE · On-site
$35.50 - $47.25/hr
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 ...
Wilmington, DE · On-site
$35.50 - $47.25/hr
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 ...
You will manage procedures and guidelines from different sponsors and/or monitoring environments (i ... clinical research monitor) or completion of PPD Drug Development Fellowship. • Valid driver ...
You will manage procedures and guidelines from different sponsors and/or monitoring environments (i ... clinical research monitor) or completion of PPD Drug Development Fellowship. • Valid driver ...
$71K - $189K/yr
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ... Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e ...
$71K - $189K/yr
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ... Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e ...
$71K - $189K/yr
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ... Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e ...
$71K - $189K/yr
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ... Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e ...
... manager and director. In addition, this position will participate in research involving the development and validation of new clinical assays. Maintains both handwritten and computerized records of ...
... manager and director. In addition, this position will participate in research involving the development and validation of new clinical assays. Maintains both handwritten and computerized records of ...
The Swank Autism Center provides comprehensive clinical services for children up to age 21 years and conducts research and community-based outreach and training. Key Responsibilities: * Develop a ...
The Swank Autism Center provides comprehensive clinical services for children up to age 21 years and conducts research and community-based outreach and training. Key Responsibilities: * Develop a ...
$49K - $61.8K
3% of jobs
$61.8K - $74.5K
13% of jobs
$79.7K is the 25th percentile. Wages below this are outliers.
$74.5K - $87.3K
22% of jobs
The median wage is $98K / yr.
$87.3K - $100K
14% of jobs
$100K - $112.7K
16% of jobs
$118.3K is the 75th percentile. Wages above this are outliers.
$112.7K - $125.5K
16% of jobs
$125.5K - $138.2K
7% of jobs
$138.2K - $150.9K
6% of jobs
$150.9K - $163.7K
2% of jobs
$163.7K - $176.4K
0% of jobs
$176.4K - $189.2K
0% of jobs
$49K
$107.4K
$189.2K
A clinical research manager oversees clinical trials, which involve testing new medications or medical devices. Their responsibilities include ensuring all ethical practices and legal protocols are followed and that all paperwork is filled out completely and accurately. They also maintain standards for the data collection and procedures during the clinical trial and make sure all team members, including the doctors and nurses on the trial, are kept informed.
| Aspect | Clinical Research Manager | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's or higher in life sciences, often with experience in project management | Bachelor's in health sciences or related field, often with certification like CCRP |
| Work Environment | Oversees multiple studies, manages teams, and ensures compliance at a higher level | Assists with daily study activities, patient interactions, and data collection |
| Employer & Industry Usage | Pharmaceutical companies, CROs, academic institutions | Hospitals, clinics, research sites |
The Clinical Research Manager focuses on overseeing entire studies and managing teams, while the Clinical Research Coordinator handles daily study tasks and participant interactions. Both roles require relevant certifications and are essential in clinical research settings, but they differ in scope and responsibilities.
The most popular types of Clinical Research jobs in Delaware are:
For Clinical Research Manager jobs in Delaware, the most frequently searched job titles are:
The top searched job categories for Clinical Research Manager jobs in Delaware are:
Cities in Delaware with the most Clinical Research Manager job openings:

Full-time
Medical, Retirement, PTO
Posted 19 hours ago
Posted today
7.8
Based on 130 frontline employees who took The Breakroom Quiz
127th of 888 rated healthcare providers
Do you want to work at one of the Top 100 Hospitals in the nation? We are guided by our values ofLoveandExcellenceand are passionate about delivering health, not just health care. Come join us at ChristianaCare!
ChristianaCare, with Hospitals in Wilmington and Newark, DE, as well as Elkton, MD, is one of the largest health care providers in the Mid-Atlantic Region. Named one of "America's Best Hospitals" by U.S. News & World Report, we have an excess of 1,100 beds between our hospitals and are committed to providing the best patient care in the region. We are proud to that Christiana Hospital, Wilmington Hospital, our Ambulatory Services, and HomeHealth have all received ANCC Magnet Recognition
PRIMARY FUNCTION:
The Director of Clinical Research at ChristianCare's Research Institute (iREACH) is part of a team leading the ongoing transformation of research across the enterprise, while fostering new and sustaining existing research collaborations and partnerships. This position will provide scientific expertise and administrative oversite for the design, planning and dissemination of a collaborative research portfolio that bridges clinical, community and academic sectors. The Director of Clinical Research will manage a team of data analysts', system engineers, biostatisticians, and Research Scientists within the Research Institute as well as within the context of the NIGMS-funded Delaware's ACCEL Center for Translational Research (DE-CTR). In the CTR arena, the Director of Clinical Research will oversee the Biostatistical and Epidemiologic Research Design (BERD) Core leveraging resources across all ACCEL Institutions to support research addressing critical health needs in Delaware. This position will represent ChristianaCare on the Data Science Core of the Delaware IDeA Network of Biomedical Research Excellence (DE-INBRE) which is supported by NIH NIGM funding.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
Responsible for oversight of the Research Institutes portfolio of research projects and related programs ensuring that all research is scientifically rigorous, clinically relevant, ethically sound and meet all institutional, state and federal rules, policies, and regulations.
Provides high level oversight of study designs, protocols, and statistical analyses to ensure scientific integrity and clinical relevance across all iREACH research projects.
Ensure all research activities comply with IRB, HIPAA, and FDA regulations. Oversee the development of Data Safety Monitoring Plans (DSMP), Data Use Agreements (DUAs), and coordinated regulatory submission for multiple institutions to ensure data privacy and security.
Serves as the Research Institutes liaison with ChristianaCare's Center for Strategic Information Management (CSIM) and responsible for ensuring the Research Institutes data processes, procedures, and permissions are met pre and post EPIC implementation.
Accountable for ensuring ChrisitanaCare's Research Institute is adhering to NIH Data Management and Sharing (DSM) Policy for all research that is supported by NIH and meets the conditions. Leads efforts with DE- CTR and DE-INBRE partner institutions and research collaborators to develop, standardize and share best practices.
Manages and provides direct supervision to a multidisciplinary team of system engineers, data analysts, biostatisticians and research scientists, fostering a culture of accountability and professional excellence.
Serve as a primary mentor for clinical and junior investigators, providing expert guidance on grant development, study design, data evaluation, interpretation and dissemination of findings.
EDUCATION AND EXPERIENCE REQUIREMENTS:
PhD in Epidemiology, Public Health, or other healthcare disciplines required.
MD, DO, RN with an advanced degree (MPH or PhD) in Epidemiology, Public Health, or Medical Informatics highly desired.
A distinguished publication record and a demonstrated history of securing and managing significant research grants required.
5+ years of leading and managing complex federally funded grants and research programs required.
5+ years of managing technical teams with proven track record of hitting hard deadlines and managing competing priorities required.
Proven success in mentoring junior faculty or clinical investigators through the research lifecycle, from protocol development to publication required.
Experience navigating the complexities of multi-institutional data sharing, IRB coordination, and collaborative analysis required.
KNOWLEDGE, SKILL, AND ABILITY REQUIREMENTS:
Advanced knowledge of health data cloud computing and data standards such FHIR, to ensure data integrity and compatibility across diverse research environments.
Strong command of statistical software (SAS, R, or Python) and deep familiarity with healthcare data structures (ICD-10, CPT, LOINC).
Deep understanding of federal research requirements and regulations including human subject research.
Exceptionally strong written and verbal skills.
Ability to promote and encourage diversity of thought.
Adept at leading in a highly complex, matrixed healthcare environment.
Christiana Care Health System is an equal opportunity employer, firmly committed to prohibiting discrimination, whose staff is reflective of its community, and considers qualified applicants for open positions without regard to race, color, sex, religion, national origin, sexual orientation, genetic information, gender identity or expression, age, veteran status, disability, pregnancy, citizenship status, or any other characteristic protected under applicable federal, state, or local law.
Post End Date
Sep 1, 2026EEO Posting Statement
ChristianaCare offers a competitive suite of employee benefits to maximize the wellness of you and your family, including health insurance, paid time off, retirement, an employee assistance program. To learn more about our benefits for eligible positions visithttps://careers.christianacare.org/benefits-compensation/
Get the full story on Breakroom
Sourced by ZipRecruiter
ChristianaCare is one of the country's most dynamic health care organizations, centered on improving health outcomes, making high-quality care more accessible and lowering health care costs. ChristianaCare includes an extensive network of outpatient services, home health care, urgent care centers, three hospitals (1,299 beds), a free-standing emergency department, a Level I trauma center and a Level III neonatal intensive care unit, a comprehensive stroke center and regional centers of excellence in heart and vascular care, cancer care and women's health. It also includes the pioneering Gene Editing Institute and was rated by IDG Computerworld as one of the nation's Best Places to Work in IT. ChristianaCare is a nonprofit teaching health system with more than 260 residents and fellows. It is continually ranked by U.S. News & World Report as a Best Hospital. With the unique CareVio data-powered care coordination service and a focus on population health and value-based care, ChristianaCare is shaping the future of health care.
Outpatient health care
10,000+ Employees
Wilmington, DE, US
1888