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Clinical Trial Associate Jobs in Delaware (NOW HIRING)

AstraZeneca

Clinical Study Administrator

Wilmington, DE

$93K - $139K/yr

... Associate's degree or an equivalent combination of education and relevant experience will be ... Experience: 1-3 years of relevant experience in clinical research, study start-up, or regulated ...

AstraZeneca

Clinical Study Administrator

Wilmington, DE · On-site

$93K - $139K/yr

... Associate's degree or an equivalent combination of education and relevant experience will be ... Experience: 1-3 years of relevant experience in clinical research, study start-up, or regulated ...

AstraZeneca

Clinical Study Administrator

Wilmington, DE · On-site

$93K - $139K/yr

... Associate's degree or an equivalent combination of education and relevant experience will be ... Experience: 1-3 years of relevant experience in clinical research, study start-up, or regulated ...

Agilent

Clinical Affairs Scientist

Wilmington, DE · On-site +1

$105K - $197K/yr

The candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance ...

CEDENT

Study Start-Up Manager

Wilmington, DE · On-site

Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up ... Ensure the timely submission of documents to regulatory authorities and maintain the trial master ...

AstraZeneca

Study Start Up Manager

Wilmington, DE

Partner closely with CRAs and the Local Study Team/Local Study Associate Director to achieve start ... of clinical trial process across Phases II-IV and ICH GCP - Good understanding of clinical ...

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Clinical Trial Associate information

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How much do clinical trial associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical trial 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 trial associate?

A clinical trial associate helps oversee late-stage drug trials. They design and implement the final clinical study before making reports to the FDA and other regulatory bodies. Their duties cover logistics, including ordering supplies, auditing all reports and documents, and ensuring their timely completion. They are responsible for making sure that the trial follows all ICH and GCP requirements.

What does a clinical trial associate do?

A Clinical Trial Associate (CTA) is responsible for supporting the planning, coordination, and management of clinical trials. They help ensure studies comply with regulatory requirements and assist in maintaining trial documentation, tracking study progress, and communicating with clinical sites. CTAs work closely with clinical research teams, sponsors, and vendors to keep trials running smoothly and efficiently. Their administrative and logistical support is essential for successful clinical research.

What are the key skills and qualifications needed to thrive as a clinical trial associate?

To thrive as a Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory guidelines, and a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, CTMS (Clinical Trial Management Systems), and GCP (Good Clinical Practice) certification are commonly required. Attention to detail, strong organizational skills, and effective communication set top performers apart in this role. These competencies are crucial for ensuring compliance, accurate data management, and smooth coordination of clinical trial activities.

What are some common challenges faced by clinical trial associates when managing study documentation?

Clinical Trial Associates often encounter challenges related to maintaining accurate and up-to-date trial documentation, as protocols and regulatory requirements can change frequently. Ensuring all documents are correctly filed, version-controlled, and accessible for audits requires strong attention to detail and organizational skills. Additionally, coordinating with multiple stakeholders—such as clinical research coordinators, data managers, and regulatory teams—can add complexity to document management. Proactive communication and adopting robust documentation systems can help overcome these challenges.

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

AspectClinical Trial AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRABachelor's degree in health sciences or related field; similar certifications
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospital, academic medical centers, clinical trial sites
ResponsibilitiesAssist in trial setup, data collection, regulatory complianceManage patient recruitment, conduct visits, data entry
Industry UsageCommon in pharmaceutical and biotech industriesCommon in hospitals and academic research settings

Both roles support clinical trials but differ mainly in scope and setting. Clinical Trial Associates typically work in industry settings focusing on trial logistics and compliance, while Clinical Research Coordinators often manage patient interactions and data at clinical sites. Understanding these differences helps in choosing the right career path or job search focus.

More about Clinical Trial Associate jobs

What are the most commonly searched types of Clinical Trial jobs in Delaware?

The most popular types of Clinical Trial jobs in Delaware are:

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For Clinical Trial Associate jobs in Delaware, the most frequently searched job titles are:

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Cities in Delaware with the most Clinical Trial Associate job openings:

What are popular job titles related to Clinical Trial Associate jobs in DE?

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Clinical Trial Associate jobs near you
Infographic showing various Clinical Trial 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

Healthcare Degree

Newark, DE • On-site

$67.90 - $216.75/hr

Other

Posted 4 days ago

Job description

Clinical trial managers are responsible for coordinating and overseeing the entire clinical research process, ensuring that studies are conducted safely, ethically, and in compliance with regulatory requirements. They play a critical role in safeguarding the integrity of research and helping bring new treatments to patients.

Typical responsibilities include:

  • Working closely with principal investigators to develop trials that meet objectives.
  • Creating and managing patient recruitment strategies.
  • Drafting study manuals and protocols.
  • Hiring and supervising clinical trial staff.
  • Collecting, interpreting, and reporting data.
  • Implementing changes to the trial structure based on feedback.
  • Composing status reports and compiling final data summaries.
  • Ensuring regulatory compliance at every stage of the trial.

Salary: According to the Bureau of Labor Statistics (May 2023), clinical trial managers earn on average $127,980 per year. 10th percentile: $67,900; 25th percentile: $86,080; 50th percentile (median): $110,680; 75th percentile: $157,640; 90th percentile: $216,750.

Qualifications: A typical career path requires a master’s degree or graduate certificate in clinical trial management or a related health field, along with at least two years of hands‑on experience in clinical trials. Knowledge of ethics, regulatory compliance, and good clinical practice (GCP) is essential. Candidates may also pursue certifications from the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SOCRA) to enhance career prospects.

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