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Clinical Study Associate Jobs in Delaware (NOW HIRING)

VCA Animal Hospital

Associate Veterinarian

Newark, DE · On-site

Join us as an Associate Veterinarian at VCA Kirkwood Animal Hospital and you'll quickly discover ... Opportunities to participate in a robust Clinical Studies program Discover Additional Benefits ...

VCA Animal Hospitals

Associate Veterinarian

Newark, DE · On-site

Join us as an Associate Veterinarian at Pike Creek Animal Hospital and you'll quickly discover that ... Opportunities to participate in a robust Clinical Studies program Discover Additional Benefits ...

VCA Animal Hospitals

Associate Veterinarian

Newark, DE · On-site

Join us as an Associate Veterinarian at VCA Kirkwood Animal Hospital and you'll quickly discover ... Opportunities to participate in a robust Clinical Studies program Discover Additional Benefits ...

QPS, LLC

Associate Scientist I - TLM

Newark, DE · On-site

$45K - $50K/yr

... studies according to study protocols, and recording study results and observations. Our TLM ... IV Clinical Research services. To meet the needs of our clients, we strive to employ talented ...

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Clinical Study Associate information

See Delaware salary details

$12

$31

$55

How much do clinical study associate jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for clinical study associate in Delaware is $31.57, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $41.63 per hour, depending on experience, location, and employer.

What are Clinical Study Associates?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

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

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

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

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What are some common challenges Clinical Study Associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.
What are the most commonly searched types of Clinical Study jobs in Delaware? The most popular types of Clinical Study jobs in Delaware are:
What are popular job titles related to Clinical Study Associate jobs in Delaware? For Clinical Study Associate jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Clinical Study Associate jobs in Delaware look for? The top searched job categories for Clinical Study Associate jobs in Delaware are:
What cities in Delaware are hiring for Clinical Study Associate jobs? Cities in Delaware with the most Clinical Study Associate job openings:
Clinical Study Associate jobs near you
Infographic showing various Clinical Study Associate job openings in Delaware as of May 2026, with employment types broken down into 9% As Needed, 39% Full Time, 49% Part Time, 2% Contract, and 1% Nights. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution, with an average salary of $65,660 per year, or $31.6 per hour.
Clinical Research Coordinator (Bilingual)

Clinical Research Coordinator (Bilingual)

Nemours Children's Health

Wilmington, DE • On-site

$23.50 - $31.25/hr

Full-time

Posted 11 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

70th of 870 rated healthcare providers

Job description

Job Description
The Center for Healthcare Delivery Science (CHDS) at Nemours Children's Health is seeking a full-time Clinical Bilingual Research Coordinator (CRC). The position is available immediately and is based in Wilmington, DE. This CRC will work primarily with J.J. Cutuli, Ph.D and will require frequent travel to New Jersey and Philadelphia.
The CRC will coordinate, implement and complete qualitative and quantitative research studies focused on developing a manualized program to identify and serve students experiencing homelessness. This position involves community-based participatory research. The CRC would be working in the context of Camden City School District in New Jersey multiple days each week. Essential RC duties include assisting the Camden City Schools Homeless Education Liaison with district operations such as updating student information systems and office administrative data for families experiencing homelessness. Bilingual (English/Spanish) language skills are essential and the CRC will sometimes assist in translating materials and engaging Spanish-speaking students and families. Additionally, the CRC will coordinate IRB submissions, recruiting study participants, obtaining informed consent, interacting with community-partners, youth, young adults and parents related to research projects, scheduling and conducting study procedures, collecting and recording study data, maintaining study records, assisting with coordinating financial contracts between community partners, participating in data collection and analysis, and the preparation of scientific presentations, manuscripts, reports, and grants.
Position Requirements:
  • Minimum of a bachelor's degree or equivalent in education, counseling, social work, or related.
    • Must effectively use Microsoft computer software. Qualitative coding experience preferred.
    • Must be able to work collaboratively with educators and community human service providers.
    • Fluent bilingual (English/Spanish) communication skills are required

Upload resume and cover letter outlining your qualifications and experience, including contact information for two references to the Nemours Job portal.
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.

What Nemours Children's Health employees say

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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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