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Study Director Jobs in Delaware (NOW HIRING)

Corteva Agriscience

Study Coordinator

Newark, DE · On-site

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 ...

AstraZeneca

Local Study Associate Director

Wilmington, DE · On-site

$32.50 - $44.50/hr

Local Study Associate Director Introduction to role The Local Study Associate Director leads the delivery of country-level clinical study commitments, guiding Local Study Teams to meet agreed ...

Net2Source (N2S)

Animal Technician

Newark, DE

$22 - $25/hr

Communicating effectively with Study Directors, peers, supervisors, and attending veterinarian * Understanding and following all relevant protocols, SOPs, GLPs, and safety guidelines * Learning and ...

Net2Source (N2S)

Animal Technician

Newark, DE

Communicate effectively with Study Directors, supervisors, veterinarians, and peers * Address QA audit findings as needed * Ensure adherence to regulatory and safety standards * Assist in development ...

AstraZeneca

Director, External Partnerships

Wilmington, DE · On-site +1

$171K - $257K/yr

The External Partnership Director develops and executes the engagement strategy for high impact ... Serve as the escalation point for performance issues for both internally and externally led studies.

AstraZeneca

Director, External Partnerships

Wilmington, DE · On-site

$171K - $257K/yr

The External Partnership Director develops and executes the engagement strategy for high impact ... Serve as the escalation point for performance issues for both internally and externally led studies.

AstraZeneca

Director, External Partnerships

Wilmington, DE · On-site

$171K - $257K/yr

The External Partnership Director develops and executes the engagement strategy for high impact ... Serve as the escalation point for performance issues for both internally and externally led studies.

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Study Director information

See Delaware salary details

$45K

$128.5K

$232.7K

How much do study director jobs pay per year?

As of Jun 9, 2026, the average yearly pay for study director in Delaware is $128,478.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,000.00 and $188,700.00 per year, depending on experience, location, and employer.

What job makes $10,000 a month without a degree?

A Study Director typically earns a salary that varies based on experience and industry, but reaching $10,000 a month without a degree is uncommon. High-paying roles in research or management may require specialized skills, certifications, or extensive experience rather than formal education. Most jobs with such income levels often demand advanced training or significant industry expertise.

What is the difference between Study Director vs Laboratory Manager?

AspectStudy DirectorLaboratory Manager
CredentialsTypically requires advanced degrees (e.g., MS, PhD) and relevant certificationsRequires relevant degrees and management experience, but not necessarily advanced research credentials
Work EnvironmentLeads specific research or regulatory studies, often in contract labs or pharmaceutical companiesOversees daily lab operations, staff, and compliance across multiple projects
Industry UsageCommonly used in GLP, clinical, and research settingsUsed broadly in laboratory settings across industries

The Study Director focuses on designing, overseeing, and ensuring the integrity of specific studies, often requiring scientific expertise. The Laboratory Manager handles overall lab operations, staff management, and compliance. Both roles are essential but differ in scope and responsibilities.

What is a Study Director?

A Study Director is the individual responsible for the overall conduct of a scientific study, particularly in regulated environments such as pharmaceuticals, chemicals, or environmental research. They oversee the planning, execution, and reporting of studies to ensure they comply with regulatory standards, such as Good Laboratory Practice (GLP). The Study Director acts as the main point of control and communication, coordinating among team members and ensuring that the study meets its scientific and regulatory objectives. Their role is critical for the integrity and quality of the data generated.

How does a Study Director typically collaborate with cross-functional teams during a research project?

As a Study Director, you play a central role in coordinating research activities by regularly collaborating with scientists, technicians, quality assurance personnel, and regulatory teams. You are responsible for ensuring all team members are aligned on study objectives, timelines, and compliance requirements. Effective communication and leadership are essential, as you facilitate meetings, delegate tasks, and resolve issues that arise to keep the project on track. This collaborative environment not only fosters professional growth but also provides valuable exposure to various scientific and operational domains within the organization.

What Is the Job of a Study Director?

As a study director, your job is to manage studies, analyze results, and interpret reports so you can deliver a summary of the findings. This work has three categories. First, on the technical side, your job includes creating the plan for the study, coordinating with other scientists, and overseeing data collection. In the administrative role, you monitor junior employees and ensure each investigation finishes within budgetary constraints. In the compliance role, you ensure that each study happens under strict safety and ethics protocols. You may be asked to run multiple studies at the same time, adding to the complexity of this position.

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

To thrive as a Study Director, you need a solid background in scientific research methods, regulatory compliance, and study protocol development, usually supported by an advanced degree in life sciences or a related field. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP) standards, and project management tools is highly valued. Strong leadership, attention to detail, and effective communication are crucial soft skills for managing cross-functional teams and ensuring study integrity. These competencies are vital to ensure regulatory adherence, data accuracy, and successful project outcomes in research environments.
More about Study Director jobs
What are the most commonly searched types of Study jobs in Delaware? The most popular types of Study jobs in Delaware are:
What are popular job titles related to Study Director jobs in Delaware? For Study Director jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Study Director jobs in Delaware look for? The top searched job categories for Study Director jobs in Delaware are:
Study Director jobs near you
Infographic showing various Study Director job openings in Delaware as of June 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, 1% Temporary, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $128,478 per year, or $61.8 per hour.
Local Study Associate Director

Local Study Associate Director

AstraZeneca

Wilmington, DE • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 11 days ago

AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 71 rated pharmaceutical

Job description

Local Study Associate Director
Introduction to role
The Local Study Associate Director leads the delivery of country-level clinical study commitments, guiding Local Study Teams to meet agreed timelines, budgets and quality standards. This role works in close alignment with Global Study Teams and local leadership to ensure that studies are designed, set up, conducted, and closed in full compliance with AstraZeneca Procedural Documents, ICH-GCP and local regulations. From feasibility and site selection through monitoring and inspection readiness, the Local Study Associate Director plays a central role in turning innovative oncology science into robust clinical evidence that can change patient outcomes. Ready to shape how complex oncology trials are delivered in practice?
Accountabilities
  • Hold overall accountability for meeting country-level study commitments, ensuring timely delivery of high-quality data.
  • Lead Local Study Teams for assigned studies, including CRAs, CSAs and other contributors, promoting collaboration, clarity of roles and strong performance.
  • Drive optimal performance and compliance of Local Study Teams with AstraZeneca Procedural Documents, ICH-GCP requirements and local regulations.
  • Oversee high-quality clinical and operational feasibility assessments for potential studies, providing robust input into study selection and design.
  • Coordinate and manage the site selection process, including identification of potential sites and investigators, initial site quality risk assessments and, where needed, Site Qualification Visits to assess suitability and quality risk.
  • Ensure timely submission of applications and documentation to Ethics Committees/IRBs and, in partnership with Regulatory Affairs, support delivery of submissions to Regulatory Authorities in line with local requirements.
  • Prepare accurate country-level financial agreements and maintain current study budgets within the clinical financial system, working closely with Director SMM or Director Country Head and Clinical Finance as appropriate.
  • Ensure effective set-up and ongoing management of studies within CTMS, eTMF, study finance systems and any other tools or local platforms required by country-specific laws and processes.
  • Oversee, manage and coordinate all monitoring activities from site activation to closure according to Monitoring Plans, reviewing monitoring visit reports and providing guidance and support to monitors.
  • Conduct co-monitoring visits, accompanied site visits and training visits with study CRAs to drive quality, consistency and development.
  • Proactively identify risks, facilitate rapid resolution of complex study issues and escalate when necessary.
  • Organize and lead regular, agenda-driven Local Study Team meetings that enable transparent communication, issue resolution and aligned decision-making.
  • Build and maintain strong working relationships with Local Study Team members, site staff and global stakeholders to support smooth study execution.
  • Report study progress, milestones, risks and mitigation plans to the Global Study Associate Director, Global Study Team and SMM/Study Operations Lead as applicable.
  • Contribute to patient recruitment strategies and maintain regular contact with investigators to support enrolment targets.
  • Develop, maintain and review a study-level country risk management plan, managing sites, stakeholders, vendors and customers to ensure timely risk identification and mitigation.
  • Coordinate closely with National Coordinating Investigator or National Lead Investigator on recruitment and other key study matters where applicable.
  • Plan and lead National Investigator Meetings in line with local codes when required.
  • Support forecasting for study timelines, resource needs, recruitment, budgeting, materials and investigational product supply.
  • Ensure set-up, updating and access to business-critical systems for Safety Reporting, Regulatory Submissions and Clinical Trial Transparency at country level.
  • Ensure accuracy and compliance of all study payments in accordance with local regulations and agreements.
  • Participate in training and coaching of new Local Study Team members to ensure quality delivery and adherence to ICH-GCP and AstraZeneca procedures.
  • Maintain the study eTMF in an inspection-ready state at all times, ensuring documentation is complete, accurate and current.
  • Plan and lead audit and regulatory inspection activities in collaboration with the Clinical Quality Associate Director and Quality Assurance teams.
  • Contribute insights to process development and continuous improvement initiatives across the organization.
  • Keep line managers regularly informed about study status, milestones, key issues and team performance.
  • Ensure full compliance with local policies, codes of ethics and business practices in all study-related activities.
  • Provide feedback on research trends, competing studies and site/investigator insights that can inform local strategy.
  • Collaborate with the local Medical Affairs team as needed to support optimal study delivery and scientific quality.
  • Actively support SMM initiatives at local, regional or global level as agreed with line management.

Essential Skills/Experience
  • Bachelor's degree in related discipline with 5+ years of previous experience in the pharmaceutical industry
  • Relevant knowledge and ability to fulfill key responsibilities, including but not limited to:
    • Drug development process and related GxP processes, International guidelines ICH-GCP, relevant country regulations, medical knowledge and ability to learn relevant AZ Therapeutic Areas, Clinical Study Management including project management, monitoring, study drug handling and data management.
  • Personal Effectiveness & Drives Accountability in Others
  • Learning Agility
  • Financial, Technology & Process Competency
  • Active Listening, Fluency in written & spoken business-level English
  • Act with Integrity & high ethical standards
  • Effectively lead a team across in-person and virtual settings to deliver shared goals, demonstrates cultural awareness
  • Identify and champion more efficient delivery of quality clinical trials with optimized cost and time
  • Ability to travel nationally/internationally as required
  • Valid driving license, if country employment requirement
  • Communication & Teamwork - Influencing, Collaboration, Impactful Site conversations
  • Effective, risk-based thinking - Plans & Aligns, Strategic thinking, Problem Solving, Critical Thinking,
  • Decision Making, Effective Issue Management
  • Clinical Study Operations (GCP) & Quality Management - RbQM: Interpreting and implementing the Monitoring Plan, Study site selection & set-up
  • Deliver Priorities Results & Impact - Project Management, Recruitment/Retention Planning & Action.

Desirable Skills/Experience
  • Bachelor's degree in the life sciences field is preferred
  • Previous experience in Clinical Operations (CRA, SrCRA) or other related fields (Medical Affairs-led or Academic-led studies) is a plus

At AstraZeneca, work connects directly to a bold ambition: transforming the lives of people living with cancer by advancing cutting-edge science into meaningful treatments. Teams collaborate across disciplines and geographies, supported by strong investment in innovation, data and technology that accelerates decision-making. Curiosity is encouraged, smart risk-taking is backed by real resources, and partnerships with leading academic centers open doors to pioneering research. Every study offers the chance to learn fast, influence strategy and build a career that has clear impact on patients who need new options most.
Ready to take ownership of country-level oncology studies that could help redefine cancer care? Apply now.
The annual base pay for this position ranges from $137,938 to $206,906. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
04-Jun-2026
Closing Date
10-Jun-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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