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Work Study Jobs in Delaware (NOW HIRING)

Corteva Agriscience

Study Coordinator

Newark, DE · On-site

Make impromptu work assignments according to the daily needs of the DRGN Study Directors and Associate Investigators, ensuring appropriate coverage for in-life activities, necropsy, and time ...

AstraZeneca

Study Start Up Manager

Wilmington, DE · Hybrid

... work cross-functionally with Contracts, Feasibility, and Study Support Services in US SM&M. - Activate study sites in compliance with AZ Procedural Documents. - Share information (metrics) on study ...

AstraZeneca

Study Start Up Manager

Wilmington, DE · Hybrid

... work cross-functionally with Contracts, Feasibility, and Study Support Services in US SM&M. - Activate study sites in compliance with AZ Procedural Documents. - Share information (metrics) on study ...

AstraZeneca

Study Start Up Manager

Wilmington, DE · On-site

... work cross-functionally with Contracts, Feasibility, and Study Support Services in US SM&M. - Activate study sites in compliance with AZ Procedural Documents. - Share information (metrics) on study ...

AstraZeneca

Study Start Up Manager

Wilmington, DE · On-site

... work cross-functionally with Contracts, Feasibility, and Study Support Services in US SM&M. - Activate study sites in compliance with AZ Procedural Documents. - Share information (metrics) on study ...

AstraZeneca

Study Contracts Manager

Wilmington, DE · Hybrid

$86.40K - $115.50K/yr

Is member of LST, work with study teams to determine priorities for meeting timelines and SIV dates. Serve as a liaison between the legal and clinical trial teams. Negotiate master templates and rate ...

AstraZeneca

Study Contracts Manager

Wilmington, DE · On-site

$86.40K - $115.50K/yr

... work with study teams to determine priorities for meeting timelines and SIV dates. • Serve as a liaison between the legal and clinical trial teams. • Negotiate master templates and rate cards ...

AstraZeneca

Study Contracts Manager

Wilmington, DE · Hybrid

$86.40K - $115.50K/yr

Is member of LST, work with study teams to determine priorities for meeting timelines and SIV dates. Serve as a liaison between the legal and clinical trial teams. Negotiate master templates and rate ...

AstraZeneca

Study Contracts Manager

Wilmington, DE · On-site

$86.40K - $115.50K/yr

... work with study teams to determine priorities for meeting timelines and SIV dates. • Serve as a liaison between the legal and clinical trial teams. • Negotiate master templates and rate cards ...

AstraZeneca

Study Contracts Manager

Wilmington, DE · Hybrid

$86.30K - $115.40K/yr

... work with study teams to determine priorities for meeting timelines and SIV dates. • Serve as a liaison between the legal and clinical trial teams. • Negotiate master templates and rate cards ...

US Tech Solutions

Specialist Study Management

Wilmington, DE · On-site

$33.75 - $45.25/hr

Good interpersonal skills and ability to work in an international team environment * Willingness and ability to train others on study administration procedures * Display excellent organization and ...

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Work Study information

See Delaware salary details

$22K

$125.4K

$206.2K

How much do work study jobs pay per year?

As of May 28, 2026, the average yearly pay for work study in Delaware is $125,398.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,100.00 and $157,100.00 per year, depending on experience, location, and employer.

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

To succeed as a Work Study, you generally need strong organizational skills, time management, and the ability to balance academic and work responsibilities, often with eligibility based on financial aid requirements. Familiarity with basic office software, campus systems, and sometimes data entry tools is typically required. Reliability, professionalism, and effective communication help students stand out in diverse campus work environments. These skills are essential for meeting job expectations, supporting campus operations, and maintaining academic performance.

How do work study positions typically balance job responsibilities with academic schedules?

Work study positions are designed to accommodate students' academic commitments, with supervisors often offering flexible scheduling and reduced hours during exam periods. Students are generally expected to communicate their class schedules and workload in advance to ensure shifts do not conflict with academic requirements. While workload varies by department, most roles emphasize efficient time management and prioritize academics, fostering a supportive environment for student employees. Many work study roles also provide opportunities to develop professional skills and network within the institution.

What are work study jobs?

Work study jobs are part-time positions offered to students, typically through a federal or institutional financial aid program, to help them earn money while attending school. These jobs are often located on campus or with approved off-campus employers and are designed to be flexible with students' class schedules. Work study positions can include roles in administrative offices, libraries, research labs, or community service organizations, and they provide valuable work experience while helping to offset educational expenses.

What jobs make $3,000 a month without a degree?

Work-study positions typically do not pay $3,000 a month; however, some freelance or gig jobs such as web development, digital marketing, or skilled trades can reach or exceed this income without a degree. These roles often require specific skills, certifications, or experience and may involve flexible schedules or remote work.

What is the difference between Work Study vs Intern?

AspectWork StudyIntern
CredentialsUsually requires enrollment in a college or universityMay require enrollment or recent graduation
Work EnvironmentOn-campus or related to academic institutionVaries; can be on-site or remote in various industries
Employer & IndustryEducational institutions, government, some nonprofitsBusinesses, organizations across multiple industries
PurposeFinancial aid and work experience for studentsGaining work experience, networking, or exploring careers

Work Study positions are primarily designed for students enrolled in college, offering financial aid and relevant work experience within academic or related environments. Internships are broader, often targeted at students or recent graduates seeking industry experience across various sectors. While both provide valuable work exposure, Work Study is more focused on supporting education costs, whereas internships emphasize career development.

What are popular job titles related to Work Study jobs in Delaware? For Work Study jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Work Study jobs in Delaware look for? The top searched job categories for Work Study jobs in Delaware are:
What cities in Delaware are hiring for Work Study jobs? Cities in Delaware with the most Work Study job openings:
Work Study jobs near you
Study Coordinator

Study Coordinator

Corteva Agriscience

Newark, DE • On-site

Full-time

Medical, Retirement, PTO

Posted 15 days ago

Job description

Who are we, and what do we do?
At Corteva Agriscience, you will help us grow what's next. No matter your role, you will be part of a team that is building the future of agriculture - leading breakthroughs in the innovation and application of science and technology that will better the lives of people all over the world and fuel the progress of humankind.
The Team Lead, In Vivo Associate Investigators will provide hands-on people leadership and oversight for technical staff within the Developmental, Reproductive, General, and Neurotoxicology (DRGN) group, partnering with Planning & Management to coordinate resources, remove execution barriers, and ensure timely, compliant study conduct and reporting. This role is expected to communicate priorities and progress to both scientific and operational stakeholders and to coach team members to deliver consistent, high-quality outcomes, while fostering a culture of safety, animal welfare, and continuous improvement. The Team Lead will help translate study plans into daily execution, proactively manage risk, and drive operational excellence across multiple concurrent studies.
What You'll Do:
  • Lead a team of 10 Associate Investigators, providing day-to-day direction, coaching, and performance support to enable consistent study execution.
  • Maintain a strong working knowledge of rodent developmental and reproductive (DART), and general toxicology study conduct, including endpoints and sample collection requirements that support downstream interpretation and reporting.
  • Coordinate with Planning & Management, Study Directors, PIs, and Technical Leads to align facility resources with DRGN study needs, anticipating constraints and rebalancing staff and space to protect critical timelines.
  • Demonstrate comprehensive understanding of Good Laboratory Practices (GLP) and ensure team execution meets applicable regulatory expectations and internal quality standards.
  • Follow well established Standard Operating Procedures (SOPs) and Guidance Documents, and reinforce documentation discipline (e.g., records, deviations, and training) to support inspection readiness.
  • Anticipate, identify, and prioritize critical needs, issues, and gaps in collaboration with DRGN Scientists and the Planning & Management staff, driving timely escalation and practical mitigation plans.
  • Make impromptu work assignments according to the daily needs of the DRGN Study Directors and Associate Investigators, ensuring appropriate coverage for in-life activities, necropsy, and time-sensitive endpoints.
  • Facilitate training programs, maintain training records, mentor team members, and foster cross training, including coaching on clear communication of technical issues and study status to scientific and operational partners.
  • Ensure completion of orientation and training records for new Associate Investigators, and verify readiness before independent task execution.
  • Partner with Study Directors, Quality Assurance, and facility leadership during audits/inspections and internal readiness reviews, supporting timely responses, investigations, and corrective/preventive actions (CAPA).

  • Drive continuous improvement by identifying recurring pain points (e.g., scheduling conflicts, documentation errors, training gaps) and implementing practical countermeasures, metrics, and standard work to improve throughput and quality.
  • Model and reinforce a strong safety and animal welfare culture, ensuring hazards are addressed, staff are trained and equipped, and in-life activities are executed with integrity and care.

What Skills You Need:
  • Ph.D. with 3-years or M.S. Degree with 10 years experience in a relevant scientific discipline (e.g., toxicology, DART, Animal Sciences or related field).
  • Comprehensive experience with rodent toxicity study conduct, including execution in a GLP environment.
  • Experience managing technical level scientists, with demonstrated ability to coordinate multiple priorities, projects, and timelines in a fast-paced environment as a people leader.
  • Hands-on experience with cesarean sections including fetal examinations and other relevant parental and fetal endpoints promulgated in OECD reproductive and developmental testing guidelines.
  • Working skills with MS Office, Instem Provantis, and other software tools, with the ability to produce clear, timely study documentation and status updates.
  • Excellent communication and organizational skills, including the ability to communicate complex technical or scheduling issues clearly to scientific and non-scientific audiences.
  • The ability to react calmly and efficiently in urgent situations, prioritizing safety, animal welfare, data integrity, and business-critical deliverables.

Benefits - How We'll Support You:
  • Numerous development opportunities offered to build your skills.
  • Be part of a company with a higher purpose and contribute to making the world a better place.
  • Health benefits for you and your family on your first day of employment.
  • Four weeks of paid time off and two weeks of well-being pay per year, plus paid holidays.
  • Excellent parental leave which includes a minimum of 16 weeks for mother and father.
  • Future planning with our competitive retirement savings plan and tuition reimbursement program.
  • Learn more about our total rewards package here - Corteva Benefits.
  • Check out life at Corteva! www.linkedin.com/company/corteva/life.

Are you a good match? Apply today! We seek applicants from all backgrounds to ensure we get the best, most creative talent on our team.
Corteva Agriscience is an equal opportunity employer. We are committed to embracing our differences to enrich lives, advance innovation, and boost company performance. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, military or veteran status, pregnancy related conditions (including pregnancy, childbirth, or related medical conditions), disability or any other protected status in accordance with federal, state, or local laws.
Benefits - How We'll Support You:
  • Numerous development opportunities offered to build your skills
  • Be part of a company with a higher purpose and contribute to making the world a better place
  • Health benefits for you and your family on your first day of employment
  • Four weeks of paid time off and two weeks of well-being pay per year, plus paid holidays
  • Excellent parental leave which includes a minimum of 16 weeks for mother and father
  • Future planning with our competitive retirement savings plan and tuition reimbursement program
  • Learn more about our total rewards package here - Corteva Benefits
  • Check out life at Corteva! www.linkedin.com/company/corteva/life

Are you a good match? Apply today! We seek applicants from all backgrounds to ensure we get the best, most creative talent on our team.
Corteva Agriscience is an equal opportunity employer. We are committed to embracing our differences to enrich lives, advance innovation, and boost company performance. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, military or veteran status, pregnancy related conditions (including pregnancy, childbirth, or related medical conditions), disability or any other protected status in accordance with federal, state, or local laws.

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