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Clinical Trials Associate Jobs in Delaware (NOW HIRING)

AstraZeneca

Clinical Study Administrator

Wilmington, DE · On-site

Interface with investigators, external service providers and Clinical Research Associates (CRAs) to ... Ability to identify and champion more efficient delivery of quality clinical trials with optimised ...

AstraZeneca

Clinical Study Administrator

Wilmington, DE · On-site

Interface with investigators, external service providers and Clinical Research Associates (CRAs) to ... Ability to identify and champion more efficient delivery of quality clinical trials with optimised ...

AstraZeneca

Clinical Study Administrator

Wilmington, DE · On-site

Interface with investigators, external service providers and Clinical Research Associates (CRAs) to ... Ability to identify and champion more efficient delivery of quality clinical trials with optimised ...

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Clinical Trials Associate information

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$17

$40

$70

How much do clinical trials associate jobs pay per hour?

As of May 28, 2026, the average hourly pay for clinical trials associate in Delaware is $40.02, according to ZipRecruiter salary data. Most workers in this role earn between $32.26 and $44.04 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Trials Associate, and why are they important?

To thrive as a Clinical Trials Associate, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, typically supported by a life sciences degree. Familiarity with systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and knowledge of Good Clinical Practice (GCP) guidelines or related certifications is important. Strong organizational skills, attention to detail, and effective communication help you excel in coordinating study activities and collaborating with diverse teams. These skills ensure accurate trial execution, regulatory adherence, and successful study outcomes.

What are some common challenges faced by Clinical Trials Associates, and how can they be managed effectively?

Clinical Trials Associates often face challenges such as coordinating with multiple stakeholders, managing tight deadlines, and ensuring strict compliance with regulatory guidelines. Balancing administrative tasks with participant communication requires strong organizational skills and attention to detail. Staying proactive in communication, utilizing project management tools, and seeking guidance from senior team members can help manage these challenges effectively while fostering a collaborative team environment.

What are Clinical Trials Associates?

Clinical Trials Associates (CTAs) are professionals who support the planning, coordination, and administration of clinical research studies, often working under the supervision of Clinical Research Coordinators or Managers. Their responsibilities typically include maintaining study documentation, ensuring regulatory compliance, assisting with data collection, and communicating with study sites. CTAs play a critical role in ensuring that clinical trials run smoothly and adhere to strict protocols and guidelines. Their work helps bring new medical treatments and therapies to market safely and efficiently.

What is the difference between Clinical Trials Associate vs Clinical Research Coordinator?

AspectClinical Trials AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRA are commonBachelor's degree in health sciences or related field; certifications like CCRP are advantageous
Work EnvironmentTypically works in clinical trial sites, pharmaceutical companies, or CROsWorks directly at clinical sites, hospitals, or research centers
Job FocusSupports trial setup, data entry, and regulatory complianceManages patient recruitment, scheduling, and data collection

While both roles support clinical research, Clinical Trials Associates primarily focus on trial logistics and compliance, whereas Clinical Research Coordinators handle patient interactions and site management. Both positions require similar educational backgrounds and certifications, often working in the same environments, but their daily responsibilities differ.

What are the most commonly searched types of Clinical Trials jobs in Delaware? The most popular types of Clinical Trials jobs in Delaware are:
What cities in Delaware are hiring for Clinical Trials Associate jobs? Cities in Delaware with the most Clinical Trials Associate job openings:
Clinical Trials Associate jobs near you
Infographic showing various Clinical Trials Associate job openings in Delaware as of May 2026, with employment types broken down into 7% As Needed, 41% Full Time, 45% Part Time, 2% Temporary, and 5% Contract. Highlights an 59% Physical, 12% Hybrid, and 29% Remote job distribution, with an average salary of $83,241 per year, or $40 per hour.
Clinical Trials Manager

Clinical Trials Manager

Nemours Children's Health

Wilmington, DE • On-site

Full-time

Posted 13 days ago

Nemours Children's Health rating

8.1

Company rating: 8.1 out of 10

Based on 86 frontline employees who took The Breakroom Quiz

71st of 864 rated healthcare providers

Job description

Job Description
Nemours is seeking a Clinical Trials Manager. The Clinical Trials Manager provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. 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 Children's Hospital- Delaware. Managing both Hematology and Oncology Research Associates, this position will support the Moseley Institute in Delaware Valley. Collaborating with Research partners across multiple Nemours sites and Non-Nemours sites this leadership role will work in conjunction with the enterprise coalition for the Nemours Center for Cancer and Blood Disorders (NCCBD).
Essential Functions:
A. Strategic Planning and Development:
1. Meet with the medical staff and faculty on a regular basis to assess their needs pertaining to clinical trials research.
2. Develop goals and performance measures in conjunction with the medical faculty to ensure growth and development of the clinical trials program.
3. Meet regularly with the Associate Administrator - Delaware to provide feedback on new initiatives, performance of on-going initiatives, and seek feedback for future programmatic development.
4. Assist with budget management of the clinical trials program in Delaware Valley
B. Supervision and Oversight:
1. Supervise and coordinate the daily activities of the research coordinators and staff.
2. Provide guidance and oversight for submissions to scientific and ethical review committees.
3. Review new research protocols and ensure there is adequate and appropriate staffing for current and planned protocols.
4. Conduct interviews and make hiring recommendations.
5. Provide oversight, periodic review including rounding, and feedback to clinical trials staff.
6. Provide procedures for systematic record keeping, drug accountability, patient interactions, equipment tracking, and good clinical practices.
7. Provide pre-review prior to external audit or investigations.
8. Responsible for performance management of designated staff.
Requirements:
  • Masters degree preferred; Bachelors degree with appropriate experience may be acceptable.
  • BSN with active Delaware Nursing License preferred.
  • Five years of Clinical Research Coordinator experience or equivalent experience required, with a minimum of 5 years clinical pediatric experience. Pediatric Oncology Clinical Research experience preferred.

About Us
Nemours Children's Health is an internationally recognized pediatric health system serving more than 1.7 million patient encounters each year. We deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships.
Backed by the Nemours Foundation and Alfred I. duPont Trust, our $1.7B nonprofit system is dedicated to improving children's health through clinical care, research, education, advocacy, and prevention. Our Whole Child Health approach focuses equally on prevention and treatment, partnering with communities to help every child thrive.
Inclusion and belonging guide our strategy and growth. We are committed to culturally relevant care, reducing health disparities, and fostering an environment where every associate, patient, and family feels supported and valued.
Learn more at Nemours.org.

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About Nemours Children's Health

Sourced by ZipRecruiter

Nemours Children’s Health, situated in Rockland, Delaware, US, operates within the healthcare industry. The company is a prominent health system offering pediatric care in Delaware, New Jersey, Pennsylvania, and Florida. It was founded in 1936 by Alfred I duPont, philanthropist and industrialist, to improve the health of children. The core values of Nemours include quality, accountability, respect, and teamwork. Its mission is to provide leadership, institutions, and services to restore and foster a healthy tomorrow for children. The non-profit organization is unique in that its primary focus is on patient families, ensuring the highest standards of pediatric care. Notably, Nemours is consistently ranked among the top children's hospitals in the US and has its own renowned research center, the Nemours Biomedical Research.

Industry

Hospitals

Company size

5,001 - 10,000 Employees

Headquarters location

Rockland, DE, US

Year founded

1936

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