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Associate Researcher Jobs in Delaware (NOW HIRING)

The Chemours Company

R&D Associate Chemist

Newark, DE

$23.75 - $31.25/hr

Chemours is seeking a R&D Associate Chemist to join our growing Thermal & Specialty Solutions team. This position will be available at the at the Chemours Discovery Hub in Newark, DE. This highly ...

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Trueseek

Litigation Associate (DE)

Wilmington, DE · On-site

$230K - $360K/yr

Litigation Associate Based in Wilmington, DE, we are a sophisticated and dynamic law firm known for ... Conduct legal research and assist in developing litigation strategy while managing discovery ...

Focus Partners Wealth

$56K - $75K/yr

Focus Partners Wealth seeks a motivated and qualified individual for the position of Tax Associate ... Gain technical knowledge by researching and learning tax laws as required. * Analyze client ...

Focus Partners Wealth

Tax Associate

Smyrna, DE · On-site

$51K - $68K/yr

Focus Partners Wealth seeks a motivated and qualified individual for the position of Tax Associate ... Gain technical knowledge by researching and learning tax laws as required. * Analyze client ...

Focus Partners Wealth

Tax Associate

Middletown, DE · On-site

$55K - $73K/yr

Focus Partners Wealth seeks a motivated and qualified individual for the position of Tax Associate ... Gain technical knowledge by researching and learning tax laws as required. * Analyze client ...

Focus Partners Wealth

Tax Associate

Wilmington, DE · On-site

$56K - $75K/yr

Focus Partners Wealth seeks a motivated and qualified individual for the position of Tax Associate ... Gain technical knowledge by researching and learning tax laws as required. * Analyze client ...

Focus Partners Wealth

$56K - $75K/yr

Focus Partners Wealth seeks a motivated and qualified individual for the position of Tax Associate ... Gain technical knowledge by researching and learning tax laws as required. * Analyze client ...

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All JobsAssociate Researcher JobsAssociate Researcher Jobs in Delaware

Associate Researcher information

See Delaware salary details

$30K

$113.2K

$164.6K

How much do associate researcher jobs pay per year?

As of Jul 23, 2026, the average yearly pay for associate researcher in Delaware is $113,199.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,100.00 and $154,100.00 per year, depending on experience, location, and employer.

What is the highest salary for a research associate?

The highest salaries for research associates can reach around $70,000 to $90,000 annually, typically in specialized fields or with extensive experience and advanced degrees. Salaries vary based on industry, location, and level of expertise, with some senior or industry-specific roles exceeding this range.

What are the key skills and qualifications needed to thrive as an Associate Researcher, and why are they important?

To thrive as an Associate Researcher, you need a strong background in scientific methodology, data analysis, and a relevant bachelor's or master's degree in your field. Familiarity with laboratory equipment, statistical software (like SPSS or R), and research management systems is typically required. Attention to detail, critical thinking, and effective communication help you collaborate and contribute meaningful insights to research projects. These skills and qualities are crucial for producing valid, reliable results and advancing the goals of research teams.

What does an associate researcher do?

An associate researcher supports research projects by collecting and analyzing data, conducting experiments, and preparing reports. They often work under the supervision of senior researchers and may use tools like statistical software or laboratory equipment to assist in research activities.

What are some common challenges Associate Researchers face when managing multiple projects simultaneously?

Associate Researchers often juggle several projects at once, which can be challenging in terms of time management and prioritization. Balancing deadlines, coordinating with various team members, and ensuring high-quality data collection and analysis requires strong organizational skills. Proactive communication with supervisors and collaborators is essential to manage expectations and address any bottlenecks early. Utilizing project management tools and regularly updating progress can help alleviate these challenges and keep research activities on track.

How much is a research associate paid?

Research associates typically earn between $45,000 and $70,000 annually, depending on experience, education, and industry. Entry-level positions may start lower, while those with advanced skills or in specialized fields can earn higher salaries. Compensation often includes benefits such as health insurance and paid time off.

What are Associate Researchers?

Associate Researchers are professionals who assist in conducting scientific studies, experiments, or investigations in a specific field. They typically work under the supervision of a principal investigator or senior researcher, helping with data collection, analysis, and documentation. Their responsibilities can also include preparing laboratory materials, conducting literature reviews, and ensuring compliance with research protocols. Associate Researchers are often found in academic, government, or private sector research settings and may have a background in science, engineering, or social sciences.

Do I need a PhD to be a research associate?

A research associate position typically does not require a PhD; most roles require at least a bachelor's or master's degree in a relevant field. However, some research roles or specialized projects may prefer or require a PhD or additional experience. Skills in data analysis, laboratory techniques, or specific tools can also be important for the role.

What is the difference between Associate Researcher vs Research Assistant?

AspectAssociate ResearcherResearch Assistant
Required CredentialsBachelor's or Master's degree, research experienceTypically Bachelor's degree, entry-level
Work EnvironmentIndependent research, data analysis, project managementSupporting research tasks, data collection
Employer & Industry UsageUniversities, research institutes, corporate R&DUniversities, labs, research projects

The main difference between an Associate Researcher and a Research Assistant lies in experience and responsibilities. Associate Researchers usually have more research experience, handle independent tasks, and contribute to project design, while Research Assistants support data collection and basic tasks. Both roles are common in academic and research settings, but Associate Researchers typically have higher qualifications and more autonomy.

What are the most commonly searched types of Researcher jobs in Delaware? The most popular types of Researcher jobs in Delaware are:
What cities in Delaware are hiring for Associate Researcher jobs? Cities in Delaware with the most Associate Researcher job openings:
Associate Researcher jobs near you
Infographic showing various Associate Researcher job openings in Delaware as of July 2026, with employment types broken down into 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $113,199 per year, or $54.4 per hour.
Senior Clinical Research Associate

Senior Clinical Research Associate

AstraZeneca

Wilmington, DE • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

15th of 74 rated pharmaceutical

Job description

This is what you will do:
The Senior Clinical Research Associate (Sr. CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The Sr. CRA works in close collaboration with (Project Management Clinical Operations (PMCO), Study Start-Up (SSU) manager, Clinical Study Assistant (CSA) and other CRAs in Country Operations Management (COM) to ensure that study commitments are achieved in a timely and efficient manner in the country level. The Sr. CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery and compliance of the study.
The Sr. CRA is responsible for the selection, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with Alexion Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.
A Sr. CRA with demonstrated skillset and experience may take on additional responsibilities and tasks as needed (eg. Lead CRA, etc).
You will be responsible for:
  • Performing selection, initiation, interim monitoring and closeout visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Clinical Monitoring Plan (CMP).
  • Driving performance at the sites. Proactively identifying and ensuring timely resolution to study-related issues and escalate them as appropriate.
  • Training, supporting and advising Investigators and site staff in study related matters, including Risk Based Quality Management (RBQM) principles.
  • Development of recruitment plans with each site and managing and supporting enrollment to ensure sites and studies meet enrollment milestones. Document recruitment barriers and mitigation plans.
  • Ensure agreed monitoring KPIs are observed and remain within the agreed quality acceptable ranges (Action Items aging, SDV metrics, Data entry metrics, query aging, MV reports metrics, etc.)
  • Preparing and finalizing monitoring visit reports in CTMS and provide timely feed-back to the Principal Investigator, including follow-up letter, within required timelines and in line with Alexion SOPs.
  • Ensuring timely collection/uploading of essential documents into the eTMF in accordance with ICH-GCP, Alexion SOPs and local requirements. Supporting/participating in regular QC checks of the eTMF
  • In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance. Tasks may include collection, preparation, review and tracking of documents for the application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start-up and for the duration of the study.
  • Contributing to the nomination and selection of potential investigators and assisting with feasibility activities
  • Collaborating with local Medical Affairs, Medical Advisor Pipeline (MAP) and other internal stakeholders, as needed.
  • Following quality issue processes by escalating systematic or serious quality issues, data privacy breaches, or ICH-GCP compliance issues to PMCO, Director COM, HCO and/or Quality Group as required.
  • Preparing for and collaborating with the activities associated with audits and regulatory inspections in liaison with PMCO, Director COM, and Quality Group.

You will need to have:
  • Minimum of 4 years of CRA monitoring experience
  • Bachelors degree in related discipline, preferably in life science, or equivalent qualification
  • Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP.
  • Excellent knowledge of relevant local regulations.
  • Good medical knowledge and ability to learn relevant Alexion Therapeutic Areas.
  • Good understanding of the drug development process.
  • Excellent understanding of Clinical Study Management including monitoring, study drug handling and data management.
  • Excellent attention to detail.
  • Excellent written and verbal communication skills.
  • Excellent collaboration and interpersonal skills.
  • Good negotiation skills.
  • Demonstrates flexibility in schedule and willingness to travel (required travel may be as high as 70% during busy periods)
  • Valid driving license

We would prefer for you to have:
  • Ability to work in an environment of remote collaborators and in a matrix reporting structure
  • Manages change with a positive approach for self, team and the business. Sees change as an opportunity to improve performance and add value to the business.
  • Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time.
  • Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.
  • Proactivity and assertive when communicating with internal stakeholders and sites
  • Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment.
  • Team oriented and flexible; ability to respond quickly to shifting demands and opportunities.
  • Experience in all study phases and in rare medical conditions preferred.

Date Posted
16-Jul-2026
Closing Date
22-Jul-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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