ZipRecruiter

Log In

1

Clinical Trials Associate Jobs in Delaware (NOW HIRING)

AstraZeneca

Clinical Research Associate

Wilmington, DE · On-site

As a Clinical Research Associate, you will be the face of AstraZeneca at investigative sites ... Identify and champion more efficient, cost- and time-optimized delivery of quality clinical trials ...

AstraZeneca

Clinical Research Associate

Wilmington, DE · On-site

As a Clinical Research Associate, you will be the face of AstraZeneca at investigative sites ... Identify and champion more efficient, cost- and time-optimized delivery of quality clinical trials ...

AstraZeneca

Clinical Research Associate

Wilmington, DE · On-site +1

As a Clinical Research Associate, you will be the face of AstraZeneca at investigative sites ... Identify and champion more efficient, cost- and time-optimized delivery of quality clinical trials ...

Agilent

Clinical Affairs Scientist

Wilmington, DE · On-site +1

$105K - $197K/yr

... Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and ... monitoring in clinical trials. * Ensure scientific validity of reported results including ...

next page

Showing results 1-20

All JobsClinical Trials Associate JobsClinical Trials Associate Jobs in Delaware

Clinical Trials Associate information

See Delaware salary details

$17

$40

$70

How much do clinical trials associate jobs pay per hour?

As of Sep 8, 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 is a clinical trials associate?

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 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 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.

Is a clinical trials associate a good career?

A clinical trials associate is a valuable role in the healthcare and pharmaceutical industries, responsible for coordinating and monitoring clinical trial activities. It offers opportunities for career growth, requires attention to detail, and often involves working with regulatory guidelines and data management tools. The role can be stable and rewarding for those interested in medical research and patient safety.

What do I need to be a clinical trials associate?

To become a clinical trials associate, candidates typically need a bachelor's degree in life sciences, healthcare, or a related field. Relevant skills include knowledge of Good Clinical Practice (GCP), attention to detail, and experience with clinical trial management systems or regulatory documentation. Certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects.

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 August 2026, with employment types broken down into 2% As Needed, 75% Full Time, 16% Part Time, and 7% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $83,241 per year, or $40 per hour.

Clinical Trials Manager

Nemours Children's Health

Wilmington, DE

Full-time

Re-posted 25 days ago

Nemours Children's Health rating

8.1

Company rating: 8.1 out of 10

Based on 88 frontline employees who took The Breakroom Quiz

68th of 898 rated healthcare providers

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.


 

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.

What Nemours Children's Health employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Nemours logo

About Nemours

Sourced by ZipRecruiter

As one of the nation's leading pediatric health care systems, Nemours is committed to providing all children with their best chance to grow up healthy. We offer integrated, family-centered care to more than 300,000 children each year in our pediatric hospitals, specialty clinics, primary care practices, and school-based health centers in Delaware, Florida, Maryland, New Jersey and Pennsylvania. Nemours strives to ensure a healthier tomorrow for all children - even those who may never enter our doors - through our world-changing research, education and advocacy efforts.

Industry

Health care and social assistance and hospitals

Company size

1,001 - 5,000 Employees

Headquarters location

Jacksonville, FL, US

View All Nemours Jobs

Apply