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 ...
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 ...
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 ...
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 ...
Collegewide Title IX Investigator
Dover, DE · On-site
$61K/yr
... manage highly sensitive and confidential information. Strong skills in the areas of conflict resolution, problem solving techniques, interviewing and investigation. Knowledge of Federal and State ...
Collegewide Title IX Investigator
Dover, DE · On-site
$61K/yr
... manage highly sensitive and confidential information. Strong skills in the areas of conflict resolution, problem solving techniques, interviewing and investigation. Knowledge of Federal and State ...
Financial Crime Risk Investigator II - OneTouch (US)
Wilmington, DE · Remote
$29.75 - $47.75/hr
Financial Crime Risk Management Department Overview: Our team currently operates under a primarily ... The Financial Crime Risk Investigator II conducts investigations of moderate complexity for both ...
Financial Crime Risk Investigator II - OneTouch (US)
Wilmington, DE · Remote
$29.75 - $47.75/hr
Financial Crime Risk Management Department Overview: Our team currently operates under a primarily ... The Financial Crime Risk Investigator II conducts investigations of moderate complexity for both ...
Clinical Research Associate
Wilmington, DE · On-site +1
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 ...
Clinical Research Associate
Wilmington, DE · On-site +1
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 ...
Contract Investigator - Newark, DE
Newark, DE · On-site +1
Current (within the last 2 years) Single Scope Background Investigation (SSBI) or active Secret ... Engage in dialogue on a regular basis with managers and representatives at contractor facilities ...
Contract Investigator - Newark, DE
Newark, DE · On-site +1
Current (within the last 2 years) Single Scope Background Investigation (SSBI) or active Secret ... Engage in dialogue on a regular basis with managers and representatives at contractor facilities ...
Contract Investigator - Newark, DE
Newark, DE · On-site
$52 - $82/hr
Current (within the last 2 years) Single Scope Background Investigation (SSBI) or active Secret ... Engage in dialogue on a regular basis with managers and representatives at contractor facilities ...
Contract Investigator - Newark, DE
Newark, DE · On-site
$52 - $82/hr
Current (within the last 2 years) Single Scope Background Investigation (SSBI) or active Secret ... Engage in dialogue on a regular basis with managers and representatives at contractor facilities ...
Associate Investigator
Newark, DE · On-site
$73.95 - $115.54/hr
Position Overview Chemours is seeking an Associate Investigator to join our growing Chemours ... Manage multiple projects simultaneously with varying degrees of priority * Safely operate and ...
Associate Investigator
Newark, DE · On-site
$73.95 - $115.54/hr
Position Overview Chemours is seeking an Associate Investigator to join our growing Chemours ... Manage multiple projects simultaneously with varying degrees of priority * Safely operate and ...
Associate Investigator
Newark, DE · On-site
$45K - $45K/yr
Chemours is seeking an Associate Investigator to join our growing Chemours Leveraged Analytical ... Manage multiple projects simultaneously with varying degrees of priority * Safely operate and ...
Associate Investigator
Newark, DE · On-site
$45K - $45K/yr
Chemours is seeking an Associate Investigator to join our growing Chemours Leveraged Analytical ... Manage multiple projects simultaneously with varying degrees of priority * Safely operate and ...
Associate Investigator
Newark, DE · On-site
Chemours is seeking an Associate Investigator to join our growing Chemours Leveraged Analytical ... Manage multiple projects simultaneously with varying degrees of priority * Safely operate and ...
Associate Investigator
Newark, DE · On-site
Chemours is seeking an Associate Investigator to join our growing Chemours Leveraged Analytical ... Manage multiple projects simultaneously with varying degrees of priority * Safely operate and ...
Preparing detailed investigative reports and presenting findings to management and prosecutorial authorities. * Ensuring compliance with agency policies, procedures, and legal requirements during all ...
Preparing detailed investigative reports and presenting findings to management and prosecutorial authorities. * Ensuring compliance with agency policies, procedures, and legal requirements during all ...
Preparing detailed investigative reports and presenting findings to management and prosecutorial authorities. * Ensuring compliance with agency policies, procedures, and legal requirements during all ...
Preparing detailed investigative reports and presenting findings to management and prosecutorial authorities. * Ensuring compliance with agency policies, procedures, and legal requirements during all ...
Risk Manager
Wilmington, DE · On-site
Investigate and address theft, fraud, vandalism, security breaches, and safety policy violations, partnering with Human Resources and management, as needed. Conduct internal theft interviews and ...
Quick apply
Risk Manager
Wilmington, DE · On-site
Investigate and address theft, fraud, vandalism, security breaches, and safety policy violations, partnering with Human Resources and management, as needed. Conduct internal theft interviews and ...
NMR Investigator, Analytical R&D Associate
Newark, DE · On-site
$45K - $46K/yr
The Chemours Company in Newark, DE is seeking an Associate Investigator for joining its Leveraged ... and project management skills. The position also includes competitive compensation and ...
NMR Investigator, Analytical R&D Associate
Newark, DE · On-site
$45K - $46K/yr
The Chemours Company in Newark, DE is seeking an Associate Investigator for joining its Leveraged ... and project management skills. The position also includes competitive compensation and ...
NMR Investigator, Analytical R&D Associate
Newark, DE · On-site
$45K - $46K/yr
The Chemours Company in Newark, DE is seeking an Associate Investigator for joining its Leveraged ... and project management skills. The position also includes competitive compensation and ...
NMR Investigator, Analytical R&D Associate
Newark, DE · On-site
$45K - $46K/yr
The Chemours Company in Newark, DE is seeking an Associate Investigator for joining its Leveraged ... and project management skills. The position also includes competitive compensation and ...
Experience in risk management, deviation and root-cause investigations and CAPAs. Experience in ... writing CMC sections of IND and BLA (Biologics License Application) Experience in formulation ...
Experience in risk management, deviation and root-cause investigations and CAPAs. Experience in ... writing CMC sections of IND and BLA (Biologics License Application) Experience in formulation ...
Overview The Senior Principal Investigator, Drug Product Process Development will report to the ... Manage and execute Primary/Registration batch manufacturing aligned with regulatory filings. * Lead ...
Overview The Senior Principal Investigator, Drug Product Process Development will report to the ... Manage and execute Primary/Registration batch manufacturing aligned with regulatory filings. * Lead ...
Job Summary (Primary function) The Research Investigator, Pharmacokinetics is responsible for ... Work with clinician, biostatistician, and data manager to provide deliverables on time. * Represent ...
Job Summary (Primary function) The Research Investigator, Pharmacokinetics is responsible for ... Work with clinician, biostatistician, and data manager to provide deliverables on time. * Represent ...
Research Investigator, Quantitative Pharmacology
Wilmington, DE · On-site
$45K - $45K/yr
Job Summary (Primary function) The Research Investigator, Pharmacokinetics is responsible for ... Work with clinician, biostatistician, and data manager to provide deliverables on time. * Represent ...
Research Investigator, Quantitative Pharmacology
Wilmington, DE · On-site
$45K - $45K/yr
Job Summary (Primary function) The Research Investigator, Pharmacokinetics is responsible for ... Work with clinician, biostatistician, and data manager to provide deliverables on time. * Represent ...
Research Investigator, Quantitative Pharmacology
Wilmington, DE · On-site
$120 - $180/hr
Job Summary (Primary function) The Research Investigator, Pharmacokinetics is responsible for ... Work with clinician, biostatistician, and data manager to provide deliverables on time. * Represent ...
Research Investigator, Quantitative Pharmacology
Wilmington, DE · On-site
$120 - $180/hr
Job Summary (Primary function) The Research Investigator, Pharmacokinetics is responsible for ... Work with clinician, biostatistician, and data manager to provide deliverables on time. * Represent ...
Investigation Manager information
See Delaware salary details
$23K - $30.3K
4% of jobs
$30.3K - $37.5K
10% of jobs
$43.3K is the 25th percentile. Wages below this are outliers.
$37.5K - $44.7K
14% of jobs
$44.7K - $52K
16% of jobs
The median wage is $58.2K / yr.
$52K - $59.2K
7% of jobs
$59.2K - $66.4K
10% of jobs
$70K is the 75th percentile. Wages above this are outliers.
$66.4K - $73.7K
29% of jobs
$73.7K - $80.9K
4% of jobs
$80.9K - $88.1K
3% of jobs
$88.1K - $95.4K
1% of jobs
$95.4K - $102.6K
2% of jobs
$23K
$61.4K
$102.6K
How much do investigation manager jobs pay per year?
As of Sep 7, 2026, the average yearly pay for investigation manager in Delaware is $61,404.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $69,100.00 per year, depending on experience, location, and employer.
What is an investigation manager?
Investigation Managers are professionals responsible for overseeing and coordinating investigative activities within an organization. They lead teams that conduct inquiries into issues such as fraud, misconduct, compliance violations, or criminal activity. Their role involves developing investigation strategies, ensuring adherence to legal and ethical standards, gathering and analyzing evidence, and preparing reports. Investigation Managers also liaise with law enforcement or regulatory agencies as needed and may recommend corrective actions based on their findings.
What are the key skills and qualifications needed to thrive as an investigation manager?
To thrive as an Investigation Manager, you need a solid background in investigative techniques, case management, and relevant legal or regulatory knowledge, often supported by a degree in criminal justice or a related field. Familiarity with case management software, digital forensics tools, and industry-specific compliance systems is typically required. Strong analytical thinking, leadership, and effective communication skills help you guide teams and handle sensitive situations with discretion. These skills and qualities are essential to ensure thorough, fair, and compliant investigations that protect organizational integrity and mitigate risk.
What are some common challenges investigation managers face when overseeing complex cases?
Investigation Managers often encounter challenges such as coordinating multi-disciplinary teams, managing large volumes of sensitive information, and ensuring that investigations remain unbiased and compliant with legal standards. Balancing the need for thoroughness with tight deadlines can be demanding, especially in high-stakes environments. Additionally, Investigation Managers must frequently adapt to evolving regulations and maintain effective communication with stakeholders, including legal counsel, HR, and external agencies.
What is the difference between Investigation Manager vs Detective?
| Aspect | Investigation Manager | Detective |
|---|---|---|
| Credentials | Relevant degrees, certifications in investigations or law enforcement | Law enforcement training, police academy certification |
| Work Environment | Corporate, private investigation firms, law firms | Police departments, law enforcement agencies |
| Employer & Industry | Private companies, legal firms, corporate security | Government, law enforcement agencies |
| Search & Comparison Intent | Understanding managerial roles in investigations | Fieldwork, case investigations, law enforcement duties |
Investigation Managers oversee investigation teams, plan strategies, and coordinate investigations within organizations, often in corporate or legal settings. Detectives typically conduct field investigations, gather evidence, and work directly on cases for law enforcement agencies. While both roles involve investigations, Investigation Managers focus on management and strategy, whereas Detectives focus on active casework.
What does an investigation manager do?
An investigation manager oversees and coordinates investigations within an organization, ensuring that cases are thoroughly examined and resolved. They plan investigation strategies, manage teams, review evidence, and ensure compliance with legal and procedural standards, often using tools like case management software. Strong leadership, analytical skills, and knowledge of investigative procedures are essential for this role.
What are the most commonly searched types of Investigation jobs in Delaware?
The most popular types of Investigation jobs in Delaware are:
What cities in Delaware are hiring for Investigation Manager jobs?
Cities in Delaware with the most Investigation Manager job openings:
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 11 days ago
AstraZeneca rating
8.4
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:
Essential Skills/Experience:
Role Required Skills
Desirable Skills/Experience:
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
27-Aug-2026
Closing Date
12-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.
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, 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
27-Aug-2026
Closing Date
12-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.
What AstraZeneca employees say
Pay
Benefits
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Workplace
Get the full story on Breakroom
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