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Contract Clinical Research Associate Jobs in Delaware

AstraZeneca

Clinical Research Associate

Wilmington, DE · On-site +1

As a Clinical Research Associate, you will be the face of AstraZeneca at investigative sites, ensuring our studies are initiated, conducted, and closed with excellence so regulators can make ...

System One

Research Associate I

Wilmington, DE · On-site

$29 - $35/hr

Contract Compensation: $29.00 - $35.00/hour Hours: 8 AM - 5 PM M-F Overview: Reputable Specialty Chemical Company is seeking a Research Associate to support the R&D and analytical testing of new ...

System One

Research Associate I

Wilmington, DE · On-site

$29 - $35/hr

Contract Compensation: $29.00 - $35.00/hour Hours: 8 AM - 5 PM M-F Overview: Reputable Specialty Chemical Company is seeking a Research Associate to support the R&D and analytical testing of new ...

System One

Research Associate I

Wilmington, DE · On-site

$29 - $35/hr

Contract Compensation: $29.00 - $35.00/hour Hours: 8 AM - 5 PM M-F Overview: Reputable Specialty Chemical Company is seeking a Research Associate to support the R&D and analytical testing of new ...

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Showing results 1-20

All JobsContract Clinical Research Associate JobsContract Clinical Research Associate Jobs in Delaware

Contract Clinical Research Associate information

See Delaware salary details

$12

$41

$69

How much do contract clinical research associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for contract clinical research associate in Delaware is $41.16, according to ZipRecruiter salary data. Most workers in this role earn between $28.89 and $52.69 per hour, depending on experience, location, and employer.

What is a contract clinical research associate?

Contract Clinical Research Associates (CRAs) are professionals who monitor clinical trials on behalf of pharmaceutical companies, contract research organizations (CROs), or other sponsors, but work on a contract or freelance basis rather than as permanent employees. Their primary responsibilities include ensuring that trials are conducted according to regulatory guidelines, monitoring data accuracy, and verifying that patient rights and safety are protected. Contract CRAs may work on multiple projects for different clients and often enjoy more flexibility in their schedules and work locations. This role requires strong organizational skills, knowledge of Good Clinical Practice (GCP), and the ability to travel to clinical sites.

What are some of the unique challenges faced by contract clinical research associates compared to permanent employees?

Contract Clinical Research Associates often need to quickly adapt to new study protocols, sponsor requirements, and team dynamics since they may work on multiple projects for different organizations. This can mean a faster onboarding process and the need to build rapport with new colleagues and site staff efficiently. Additionally, contract CRAs must be highly organized to manage shifting assignments and maintain compliance across different trial sites, as well as keep up with varying documentation standards. While this variety can be rewarding, it can also present challenges in terms of consistency and long-term project ownership.

What are the key skills and qualifications needed to thrive as a contract clinical research associate, and why are they important?

To thrive as a Contract Clinical Research Associate, you need a solid understanding of clinical trial protocols, regulatory guidelines (such as GCP and ICH), and typically a degree in life sciences or related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are highly valued. Strong attention to detail, organizational skills, and effective communication help build productive site relationships and ensure compliance. These skills are crucial for maintaining data integrity, ensuring regulatory adherence, and supporting successful clinical trial outcomes.

What is the difference between Contract Clinical Research Associate vs Clinical Research Associate?

AspectContract Clinical Research AssociateClinical Research Associate
CredentialsTypically requires a degree in life sciences and relevant certificationsSame as Contract CRA, often with additional experience
Work EnvironmentTemporary, project-based assignments often with multiple sponsorsFull-time employment with a single organization or sponsor
Employer & Industry UsageUsed by CROs and pharma companies for short-term projectsCommonly employed directly by pharmaceutical companies or CROs
Search & Comparison IntentOften compared for flexibility and contract work benefitsViewed as a permanent role with career growth

In summary, Contract Clinical Research Associates work on temporary, project-specific basis, often with multiple sponsors, offering flexibility. Clinical Research Associates typically hold full-time roles within a single organization, providing stability and career development opportunities.

What are popular job titles related to Contract Clinical Research Associate jobs in Delaware?

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

What job categories do people searching Contract Clinical Research Associate jobs in Delaware look for?

The top searched job categories for Contract Clinical Research Associate jobs in Delaware are:

What cities in Delaware are hiring for Contract Clinical Research Associate jobs?

Cities in Delaware with the most Contract Clinical Research Associate job openings:

Contract Clinical Research Associate jobs near you
Infographic showing various Contract Clinical Research 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 $85,616 per year, or $41.2 per hour.

Clinical Research Associate

AstraZeneca

Wilmington, DE • On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 10 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

23rd of 86 rated pharmaceutical

Job description

Are you ready to turn rigorous site execution into faster access to life-changing medicines for patients? As a Clinical Research Associate, you will be the face of AstraZeneca at investigative sites, ensuring our studies are initiated, conducted, and closed with excellence so regulators can make decisions with confidence.
In this role, you will drive the quality, speed, and integrity of clinical delivery across assigned sites. You will combine risk-based insight with hands-on partnership, building trusted relationships with investigators and site staff while keeping participant safety and data robustness at the forefront. Do you thrive on solving problems in real time and translating complex protocols into confident, compliant site performance?
From day one, you will contribute to a nimble, outcome-focused team that values curiosity, accountability, and collaboration. Your impact will be tangible-measured in inspection-ready sites, reliable data, strong recruitment, and study milestones achieved on schedule.
Accountabilities:
  • Site Readiness and Initiation: Qualify and select investigators; manage start-up activities as required, including document preparation, ethics/regulatory submissions, and site initiation. Ensure site teams complete all required training and remain inspection-ready throughout the study.
  • Risk-Based Monitoring: Plan and conduct remote and onsite monitoring visits per the Monitoring Plan; perform source data verification/review; complete remote data checks; use Site Quality Risk Assessments to adjust monitoring intensity and focus on what matters most.
  • Data Quality and Systems Excellence: Maintain up-to-date, accurate entries in CTMS and other systems; collaborate with data management to resolve queries promptly; prepare clear, timely monitoring reports and follow-up letters; collect and quality-check essential documents in the eTMF.
  • Patient Safety Oversight: Ensure accurate and prompt reporting of Serious Adverse Events and follow-up; verify protocol adherence; safeguard participant rights, privacy, and wellbeing at every step.
  • Site Performance and Recruitment: Track and drive enrollment and retention; proactively identify risks and issues; implement corrective and preventive actions; escalate appropriately; follow through to resolution to protect timelines and quality.
  • Investigational Product and Materials: Manage study supplies and the Investigator Site File; oversee investigational product accountability and preparation for destruction, where applicable.
  • Compliance and Inspection Readiness: Adhere to ICH-GCP, local regulations, and AstraZeneca procedures; escalate quality or compliance concerns; prepare sites and collaborate during audits and regulatory inspections.
  • Stakeholder Collaboration: Engage actively with the Local Study Team and investigators; contribute to investigator meetings; communicate progress and insights; share site intelligence that informs strategy; collaborate with cross-functional colleagues as directed.
  • Continuous Improvement: Identify and champion more efficient, cost- and time-optimized delivery of quality clinical trials; apply risk-based thinking to streamline processes and improve outcomes over the course of the study.

Essential Skills/Experience:
  • Bachelor's degree in related discipline, preferably in life science, or equivalent qualification aligned to the knowledge and skills of the role and ensures successful conduct of responsibilities and appropriate interactions with internal and or external stakeholders.
  • Relevant knowledge and ability to fulfil key responsibilities, including but not limited to: Drug development process, international guidelines ICH-GCP, relevant country regulations, medical knowledge and ability to learn relevant AZ Therapeutic Areas, Clinical Study Management including monitoring, study drug handling and data management.

Role Required Skills
  • Personal Effectiveness & Drives Self-Accountability
  • Learning Agility
  • Financial, Technology & Process Competency
  • Active Listening, Fluency in written & spoken business-level English
  • Act with Integrity & high ethical standards
  • Effectively work as part of a team, in person and virtual settings, demonstrates cultural awareness
  • Identify and champion more efficient delivery of quality clinical trials with optimised cost and time.
  • Ability to travel nationally/internationally as required.
  • Valid driving license, if country employment requirement
  • Communication & Teamwork - Impactful Site conversations
  • Effective, risk-based thinking - Plans & Aligns, Strategic thinking, Problem Solving, Critical Thinking, Decision Making, Effective Issue Management
  • Ethical & Participant Safety Considerations - Interpret and Implement the Clinical Study Protocol; Adhere to Participant Rights, Privacy and Wellbeing; Participant Safety Oversight and Reporting
  • Clinical Study Operations (GCP) & Quality Management - Audit & Inspection Readiness, RbQM: Interpreting and implementing the Monitoring Plan; Source Documentation and Effective Source Data Verification/Review (SDV/SDR)
  • Deliver Priorities Results & Impact: Recruitment/Retention Planning & Action.

Desirable Skills/Experience:
  • Prior experience delivering multi-center clinical studies as a CRA across phases.
  • Hands-on experience with CTMS, eTMF, and risk-based monitoring, including remote monitoring approaches.
  • Experience in start-up activities and submissions to Ethics Committees/IRBs and Regulatory Authorities.
  • Exposure to audits and inspections with proven inspection-readiness practices.
  • Certification such as ACRP-CCRA or SOCRA.
  • Strong command of local language(s) in addition to English.
  • Experience across multiple therapeutic areas and complex protocols.
  • Comfort with data analytics or digital tools used in clinical operations.

Why AstraZeneca:
Join a science-led organization where your fieldwork directly accelerates decisions that bring new medicines to people who need them. You will collaborate closely with colleagues across development, often bringing diverse experts together to challenge ideas and move faster with balanced risk. We value curiosity alongside accountability and kindness; leaders remove barriers so you can focus on what matters-patient safety, data quality, and timely delivery. With modern tools, a culture that welcomes bold thinking, and opportunities to grow across varied projects, your contributions will shape both our pipeline and your career.
Seize this opportunity to elevate your impact-help deliver confident, fast approvals by turning exceptional site execution into better outcomes for patients and your own growth.
The annual base pay (or hourly rate of compensation) for this position ranges from $112,154.40 - $168,231.60 USD Annual, either as annual base pay or as the hourly rate (annual base pay divided by 2080 hours)]. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
Date Posted
26-Aug-2026
Closing Date
25-Sep-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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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB

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