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General Studies Associate Degree Jobs in Delaware

AstraZeneca

Study Start Up Manager

Wilmington, DE · On-site

Essential Skills/Experience: - Bachelors Degree and a minimum of 3+ years of current/recent ... Step into a role where your expertise activates studies faster and strengthens approvals-bring your ...

AstraZeneca

Study Start Up Manager

Wilmington, DE · On-site

Essential Skills/Experience: - Bachelors Degree and a minimum of 3+ years of current/recent ... Step into a role where your expertise activates studies faster and strengthens approvals-bring your ...

Corteva Agriscience

Study Coordinator

Newark, DE · On-site

... General, and Neurotoxicology (DRGN) group, partnering with Planning & Management to coordinate ... studies. What You'll Do: * Lead a team of 10 Associate Investigators, providing day-to-day ...

AstraZeneca

Clinical Study Administrator

Wilmington, DE · On-site

$93K - $139K/yr

The SSU CSA assists in the coordination and administration of study activities from Site Selection ... Associate's degree or an equivalent combination of education and relevant experience will be ...

AstraZeneca

Clinical Study Administrator

Wilmington, DE · On-site

$93K - $139K/yr

The SSU CSA assists in the coordination and administration of study activities from Site Selection ... Associate's degree or an equivalent combination of education and relevant experience will be ...

QPS, LLC

Associate Scientist I - TLM

Newark, DE · On-site

... studies according to study protocols, and recording study results and observations. Our TLM ... If you have a Bachelor's degree in Biology, Biochemistry, Immunology or other related disciplines ...

Bayhealth

Nuclear Medicine Technologist

Milford, DE · On-site

As Needed SALARY RANGE: 39.88 - 61.81 HOURLY General Summary: Under the direction of the Site ... Education: Associate Degree; Nuclear Medicine; Or Associate's Degree - Radiologic Technologies.

CEDENT

Study Start-Up Manager

Wilmington, DE

Lead and manage start-up activities for clinical studies, ensuring compliance with local and ... Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up ...

Truvolt Brands LLC

General Warehouse Associate

New Castle, DE · On-site

$14.75 - $17.50/hr

General Warehouse Associate Job Type: Full Time/On-Site Job Location: New Castle, DE Nice to meet ... High degree of attention required to prevent injury to others; promote a safe work environment

Truvolt Brands LLC

General Warehouse Associate

New Castle, DE · On-site

$14.75 - $17.50/hr

General Warehouse Associate Job Type: Full Time/On-Site Job Location: New Castle, DE Nice to meet ... High degree of attention required to prevent injury to others; promote a safe work environment

Bayhealth

Teacher

Dover, DE · On-site

Day/ Evening 8am-5pm SALARY RANGE: 18.73 - 28.09 HOURLY General Summary: Performs a wide variety of ... In lieu of related degree, may have an Associate's Degree in another field of study and transcript ...

Bayhealth

Ultrasound Technologist

Dover, DE · On-site

Days SALARY RANGE: 37.07 - 57.47 HOURLY General Summary: Under the direction of the Site Manager ... Associate Degree; Allied Health; Or completion of a Certificate Program in Ultrasound studies.If ...

Bayhealth

Ultrasound Technologist

Milford, DE · On-site

Variable SALARY RANGE: 37.07 - 57.47 HOURLY General Summary: Under the direction of the Site ... Associate Degree; Allied Health; Or completion of a Certificate Program in Ultrasound studies.If ...

Bayhealth

Ultrasound Technologist

Milford, DE · On-site

Variable SALARY RANGE: 37.07 - 57.47 HOURLY General Summary: Under the direction of the Site ... Associate Degree; Allied Health; Or completion of a Certificate Program in Ultrasound studies.If ...

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All JobsGeneral Studies Associate Degree JobsGeneral Studies Associate Degree Jobs in Delaware

General Studies Associate Degree information

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How much do general studies associate degree jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for general studies associate degree in Delaware is $16.17, according to ZipRecruiter salary data. Most workers in this role earn between $14.66 and $17.31 per hour, depending on experience, location, and employer.

What is a general studies associate degree?

A General Studies Associate Degree is a two-year undergraduate program that provides students with a broad foundation in various academic subjects, including humanities, social sciences, mathematics, and natural sciences. This degree is designed for those who want flexibility in their educational path or are undecided about a specific major. Graduates can use the degree to transfer to a four-year college, explore diverse career options, or gain general skills for the workforce. The curriculum typically emphasizes critical thinking, communication, and problem-solving skills.

What types of entry-level roles are commonly available to graduates with a general studies associate degree, and how can this degree support career advancement?

Graduates with a General Studies Associate Degree often find entry-level opportunities in administrative support, customer service, sales, and roles within educational or nonprofit organizations. This degree provides a broad academic foundation and essential soft skills like communication, critical thinking, and adaptability, making graduates competitive for a wide range of positions. Additionally, many employers value the versatility and willingness to learn demonstrated by General Studies graduates. The degree also serves as a stepping stone, allowing individuals to transfer credits toward a bachelor's program or specialize further as their career interests develop.

What are the key skills and qualifications needed to thrive with a general studies associate degree, and why are they important?

To thrive with a General Studies Associate Degree, you need broad foundational knowledge in critical thinking, communication, and basic quantitative skills, typically gained through a diverse curriculum. Familiarity with productivity software like Microsoft Office and basic research tools is common, and some roles may benefit from certifications in areas such as project management or digital literacy. Strong adaptability, time management, and interpersonal skills help graduates stand out in varied workplace settings. These skills and qualities are crucial for successfully transitioning into a wide range of entry-level jobs or further academic pursuits where versatility and effective communication are valued.

What is the difference between General Studies Associate Degree vs Paralegal?

AspectGeneral Studies Associate DegreeParalegal
Required CredentialsAssociate degree in general studies or related fieldAssociate degree or certificate in paralegal studies
Work EnvironmentVaries across multiple industries; entry-level rolesLaw firms, corporate legal departments, government agencies
Industry UsageBroad; applicable in many sectorsLegal industry specific
Common Search/ComparisonYesYes

The General Studies Associate Degree provides a broad educational foundation suitable for various entry-level roles across industries. In contrast, a Paralegal certification or degree specializes in legal support tasks. While both may require an associate-level credential, the General Studies degree offers flexibility, whereas the Paralegal credential prepares you specifically for legal assistant roles.

What is a general studies associate degree good for?

A general studies associate degree provides a foundation for entry-level positions across various fields such as administration, customer service, and retail. It also serves as a stepping stone for transferring to a four-year college or university to pursue a bachelor's degree, enhancing career advancement opportunities.

What are popular job titles related to General Studies Associate Degree jobs in Delaware?

For General Studies Associate Degree jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching General Studies Associate Degree jobs in Delaware look for?

The top searched job categories for General Studies Associate Degree jobs in Delaware are:

What cities in Delaware are hiring for General Studies Associate Degree jobs?

Cities in Delaware with the most General Studies Associate Degree job openings:

General Studies Associate Degree jobs near you
Infographic showing various General Studies Associate Degree job openings in Delaware as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 10% Part Time, and 2% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $33,643 per year, or $16.2 per hour.

Clinical Research Associate, Cell Therapy - Mid Atlantic

Wilmington, DE • On-site

AstraZeneca
Pharmaceutical Product Wholesalers • 10K+ employees

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical

People enjoy working here

Good employer

Recommended by students

Learn more about AstraZenecaexternal

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 8 days ago

Job description

The Clinical Research Associate (CRA) has local responsibility for the delivery of studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficient manner. The CRA acts as the primary contact with study sites and is responsible for monitoring study conduct to ensure proper delivery of clinical trials.
This is a field-based position with a strong preference for candidates residing within the Mid-Atlantic region, including Maryland, Virginia, Washington D.C., Delaware, Pennsylvania, and New Jersey.
The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies in compliance with AstraZeneca Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations, ensuring that sites deliver according to study commitments.
A CRA with longer tenure and experience may take on additional responsibilities, including tasks associated with the Local Study Associate Director (LSAD) role.
Typical Accountabilities
  • Contributes to the selection of potential investigators.

  • Supports study start-up and regulatory maintenance activities, including Site Qualification Visits (SQVs), collection and review of regulatory documents, and submission activities to EC/IRB and Regulatory Authorities as applicable.

  • Trains, supports, and advises investigators and site staff on study-related matters, including Risk Based Quality Management (RbQM) principles.

  • Confirms site staff have completed required training, including ICH-GCP training, prior to and throughout the study duration. Ensures sites remain inspection ready at all times.

  • Actively participates in Local Study Team (LST) meetings.

  • Contributes to Investigator Meetings as applicable.

  • Initiates, monitors, and closes study sites in compliance with AstraZeneca Procedural Documents. Shares updates on patient recruitment and site performance within the LST.

  • Drives site performance by proactively identifying, resolving, and escalating study-related issues as appropriate.

  • Updates CTMS and other clinical systems within required timelines.

  • Manages study supplies, ISF documentation, investigational product accountability, and study drug reconciliation/destruction activities where applicable.

  • Performs onsite and remote monitoring visits, including remote data review activities, in accordance with study-specific Monitoring Plans.

  • Performs Source Data Review (SDR), Source Data Verification (SDV), and CRF review activities.

  • Conducts Site Quality Risk Assessments and adjusts monitoring intensity accordingly throughout the study.

  • Ensures timely resolution of data queries and collaborates with Data Management to maintain high-quality study data.

  • Ensures accurate and timely reporting of Serious Adverse Events (SAEs) and follow-up documentation.

  • Prepares and finalizes monitoring visit reports and follow-up letters within required timelines and in accordance with AstraZeneca SOPs.

  • Follows up on outstanding site actions to ensure timely resolution.

  • Escalates significant quality issues, compliance concerns, data privacy breaches, or ICH-GCP deviations to Local Management and/or Quality teams as required.

  • Assists sites in maintaining inspection-ready Investigator Site Files (ISF).

  • Supports audit and regulatory inspection readiness activities in collaboration with LSAD and Quality teams.

  • Ensures timely collection and upload of essential documents into the eTMF in compliance with ICH-GCP, AstraZeneca SOPs, and local requirements.

  • Ensures study documentation is complete and ready for final archiving activities.

  • Provides insights regarding investigators, sites, and competing studies relevant to the local market.

  • Ensures compliance with AstraZeneca's Code of Ethics and company policies related to Safety, Health & Environment (SHE), security, technology, finance, and people practices.

  • Ensures compliance with local, national, and regional regulations as applicable.

  • Collaborates with local Medical Science Liaisons (MSLs) as directed by LSAD or line management.

Minimum Qualifications
  • Bachelor's degree in Life Sciences or related discipline, or equivalent qualification.

  • Minimum 3 years of CRA or similar relevant clinical research experience within the pharmaceutical, biotechnology, or CRO industry.

  • Excellent knowledge of ICH-GCP guidelines and basic knowledge of GMP/GDP.

  • Good knowledge of relevant local regulations and clinical trial requirements.

  • Strong medical and scientific aptitude with the ability to learn AstraZeneca therapeutic areas.

  • Basic understanding of the drug development process.

  • Good understanding of Clinical Study Management, including site monitoring, study drug handling, and data management.

  • Strong attention to detail and documentation accuracy.

  • Excellent written and verbal communication skills.

  • Strong collaboration, interpersonal, and relationship-building skills.

  • Good negotiation and conflict-resolution skills.

  • Ability to travel nationally and internationally as required.

Desirable Qualifications
  • Clinical trial or relevant experience in Cell Therapy preferred. Ability to work effectively in an environment with remote collaborators and cross-functional teams.

  • Positive and adaptable approach to change management.

  • Ability to identify and champion process improvements that increase efficiency and quality.

  • Strong analytical and problem-solving capabilities.

  • Ability to prioritize and manage multiple competing deadlines effectively.

  • Familiarity with risk-based monitoring methodologies, including remote monitoring.

  • Good cultural awareness and ability to work within global teams.

  • Proficiency with clinical systems, software platforms, and technology-enabled environments.

  • Team-oriented, flexible, and responsive to shifting priorities and business needs.

Why AstraZeneca?
At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We're on an exciting journey to pioneer the future of healthcare.
So, what's next?
Are you already imagining yourself joining our team? Good, because we can't wait to hear from you!
The annual base pay for this position ranges from $112,154.40 - $168,231.60. 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
24-Aug-2026
Closing Date
17-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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