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Drug Safety Associate Jobs in Delaware (NOW HIRING)

Safety Manager

Wilmington, DE · On-site

$45 - $55/hr

Safety Manager (Underground construction) Location: Wilmington, DE Schedule: 7am-3:30pm Start Date: ASAP Pay Range: $45.00/hr- $55.00/hr Per diem available if a traveler Diversified Safety Services ...

Pharmacovigilance Safety Manager Full Time Regular Sr Professiona-Other Newark, DE, US 7 days ago ... drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology ...

Implement safety policies and procedures through direct interaction and group training. * Inspect work sites to ensure working conditions are compliant with OSHA standards and Port Wilmington safety ...

Safety Specialist

Wilmington, DE · On-site

$80K - $90K/yr

Job Overview - Safety Specialist Compensation: $80,000 - $90,000/year + bonus Location: Wilmington, DE Schedule: Monday to Friday (In-Office) Atlantic Group is hiring a Safety Specialist in ...

Safety Manager

Wilmington, DE · On-site

$127 - $159/hr

Construction Safety Manager Location: Wilmington, DE Duration: 5 Months (Start: 9/14) Type: 1099 Contractor Compensation & Schedule Pay Rate: $70/hr Overtime: Available as Project Demands Require Per ...

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Drug Safety Associate information

See Delaware salary details

$12

$49

$85

How much do drug safety associate jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for drug safety associate in Delaware is $49.19, according to ZipRecruiter salary data. Most workers in this role earn between $38.51 and $55.58 per hour, depending on experience, location, and employer.

What is a drug safety associate?

Drug Safety Associates are professionals responsible for monitoring and evaluating the safety of pharmaceutical products. They collect, analyze, and report data on adverse drug reactions to ensure compliance with regulatory requirements and to protect patient safety. Their work involves reviewing case reports, maintaining safety databases, and communicating safety information to regulatory agencies and healthcare professionals. Drug Safety Associates play a vital role in the pharmacovigilance process throughout the lifecycle of a drug.

What does a drug safety associate do?

A drug safety associate works in the medical industry to monitor the safety of pharmaceutical drugs and to evaluate and prevent adverse reactions in patients. A career in drug safety, also called pharmacovigilance, can include work with clinical research organizations that conduct trials, biotechnology firms, pharmaceutical companies, or government agencies like the National Institutes of Health (NIH). Drug safety associates need excellent research skills, a strong background in medical or biological science, and in-depth knowledge of the Food and Drug Administration (FDA) regulations. Your responsibilities include analyzing clinical trial data, writing reports, and determining whether specific pharmaceutical drugs are safe.

What are the key skills and qualifications needed to thrive as a Drug Safety Associate, and why are they important?

To thrive as a Drug Safety Associate, you need a solid background in life sciences or pharmacy, knowledge of pharmacovigilance principles, and attention to detail. Familiarity with drug safety databases (such as Argus or ARISg), MedDRA coding, and regulatory reporting systems is typically required. Strong organizational skills, effective communication, and the ability to work under deadlines help you excel in collaborating with cross-functional teams. These skills ensure accurate adverse event reporting, regulatory compliance, and protection of patient safety throughout the drug development lifecycle.

How does a drug safety associate typically collaborate with other teams during the drug development process?

Drug Safety Associates regularly work in close coordination with clinical research, regulatory affairs, and medical affairs teams. They are responsible for collecting, evaluating, and reporting adverse event data, which often requires clear communication with clinical trial staff and investigators. Additionally, they may participate in cross-functional safety review meetings to discuss safety findings and ensure compliance with regulatory requirements. This collaborative environment helps ensure comprehensive safety monitoring throughout the drug's lifecycle.

What is the difference between Drug Safety Associate vs Pharmacovigilance Specialist?

AspectDrug Safety AssociatePharmacovigilance Specialist
CredentialsTypically requires a degree in life sciences or healthcare, with certifications like PV or drug safety trainingSimilar credentials, often with additional certifications or experience in pharmacovigilance
Work EnvironmentPharmaceutical companies, CROs, or healthcare settings focusing on safety data managementSame as Drug Safety Associate, often with more specialized pharmacovigilance tasks
Employer & IndustryPharmaceutical, biotech, and healthcare industriesSame industries, with a focus on drug safety monitoring and compliance

Both roles involve monitoring drug safety data, reporting adverse events, and ensuring regulatory compliance. The main difference lies in the scope and specialization, with Pharmacovigilance Specialists often handling more complex safety data analysis and regulatory submissions. However, the roles overlap significantly, and job titles are sometimes used interchangeably depending on the organization.

What are the most commonly searched types of Drug Safety jobs in Delaware?

The most popular types of Drug Safety jobs in Delaware are:

What are popular job titles related to Drug Safety Associate jobs in Delaware?

For Drug Safety Associate jobs in Delaware, the most frequently searched job titles are:

What cities in Delaware are hiring for Drug Safety Associate jobs?

Cities in Delaware with the most Drug Safety Associate job openings:

Infographic showing various Drug Safety Associate job openings in Delaware as of August 2026, with employment types broken down into 100% Full Time. Highlights an 74% In-person, and 26% Remote job distribution, with an average salary of $102,305 per year, or $49.2 per hour.

HSE Risk and Controls Associate (Delaware/Atlanta/Princeton)

BlackRock

Wilmington, DE • On-site

Full-time

Medical, Retirement

Re-posted 10 days ago


BlackRock rating

7.8

Company rating: 7.8 out of 10

Based on 14 frontline employees who took The Breakroom Quiz


Job description

About this role

Your Team

The Health, Safety & Environment (HSE) team is responsible for maintaining a safe, compliant, and resilient workplace across the organization's global footprint. The team partners closely with Regulatory, Legal, Facilities, and regional stakeholders to identify and manage risk, strengthen governance, and drive the consistent execution of HSE programs and compliance requirements.

Your Role and Impact

As an HSE Risk & Controls Associate, you will play a critical role in advancing the organization's global HSE risk and control framework. You will help translate regulatory obligations and enterprise requirements into effective operational controls, ensuring programs operate consistently, are supported by high-quality evidence, and deliver sustainable, auditable outcomes.

In this role, you will work across regions and functions to enhance control effectiveness, strengthen compliance processes, improve risk visibility, and support a culture of accountability and continuous improvement. Your contributions will help ensure HSE programs remain scalable, effective, and aligned with evolving regulatory expectations.

Your Responsibilities

  • Support the development, implementation, and continuous enhancement of the global HSE risk and control framework, ensuring clear alignment between regulatory requirements, internal standards, risks, and controls.

  • Translate regulatory obligations and enterprise requirements into practical, scalable controls that can be embedded within HSE programs and operational processes.

  • Maintain and enhance control inventories and control-mapping documentation linking requirements, policies, procedures, risks, and controls.

  • Define evidence requirements and promote consistent documentation standards to support compliance and audit readiness across regions.

  • Review and validate control evidence, including permits, inspections, risk assessments, and training records, to confirm completeness, accuracy, and effectiveness.

  • Support the maintenance of accurate and complete records within enterprise systems of record and compliance platforms.

  • Conduct control design and operating effectiveness assessments to evaluate whether controls are functioning as intended and mitigating risk appropriately.

  • Support assurance reviews, thematic assessments, and targeted evaluations of key risk areas to strengthen the overall control environment.

  • Identify control deficiencies, compliance risks, execution inconsistencies, and process improvement opportunities, and partner with stakeholders to implement sustainable solutions.

  • Analyze trends and findings from audits, inspections, risk assessments, and regulatory reviews to identify recurring issues, emerging risks, and systemic control concerns.

  • Support oversight of core HSE programs to ensure controls are operating effectively and delivering intended risk management outcomes.

  • Assist in developing, tracking, and validating corrective and preventive action plans, ensuring remediation activities address root causes and are supported by appropriate evidence.

  • Monitor remediation progress, escalate risks when appropriate, and help drive timely resolution of identified issues.

  • Develop reporting, dashboards, and performance metrics that provide actionable insights on compliance coverage, risk exposure, issue management, and control maturity.

  • Partner with Legal, Regulatory, and regional HSE stakeholders to promote consistency in control implementation, evidence management, and compliance practices globally.

  • Provide guidance and support to stakeholders on effective control execution, documentation expectations, and continuous improvement opportunities.

Your Experience

  • Bachelor's degree in Occupational Health & Safety, Environmental Science, Engineering, Risk Management, or a related discipline.

  • 4-8 years of relevant experience in HSE compliance, regulatory affairs, risk management, governance, controls, audit, or related disciplines.

  • Experience supporting the design, implementation, testing, or oversight of risk and control frameworks.

  • Strong understanding of compliance programs, operational risk management principles, and control governance practices.

  • Demonstrated ability to interpret regulatory requirements and translate them into practical business processes and controls.

  • Experience evaluating documentation and evidence to support compliance, assurance, and audit-readiness activities.

  • Strong analytical and problem-solving skills with the ability to identify trends, assess risk, and drive improvements.

  • Excellent communication and stakeholder management skills, with the ability to influence and collaborate across functions and regions.

  • Experience developing reports, dashboards, and key performance metrics using data analysis and visualization tools.

  • Familiarity with compliance, governance, risk management, or workflow management systems is preferred.

For Princeton, NJ and Atlanta, GA Only the salary range for this position is USD$80,000.00 - USD$105,000.00 . Additionally, employees are eligible for an annual discretionary bonus, and benefits including healthcare, leave benefits, and retirement benefits. BlackRock operates a pay-for-performance compensation philosophy and your total compensation may vary based on role, location, and firm, department and individual performance. For Wilmington, DE Only the salary range for this position is USD$75,000.00 - USD$100,000.00 . Additionally, employees are eligible for an annual discretionary bonus, and benefits including healthcare, leave benefits, and retirement benefits. BlackRock operates a pay-for-performance compensation philosophy and your total compensation may vary based on role, location, and firm, department and individual performance.

Our benefits
To help you stay energized, engaged and inspired, we offer a wide range of benefits including a strong retirement plan, tuition reimbursement, comprehensive healthcare, support for working parents and Flexible Time Off (FTO) so you can relax, recharge and be there for the people you care about.

Our hybrid work model

BlackRock's hybrid work model is designed to enable a culture of collaboration and apprenticeship that enriches the experience of our employees, while supporting flexibility for all. Employees are currently required to work at least 4 days in the office per week, with the flexibility to work from home 1 day a week. Some business groups may require more time in the office due to their roles and responsibilities. We remain focused on increasing the impactful moments that arise when we work together in person - aligned with our commitment to performance and innovation. As a new joiner, you can count on this hybrid model to accelerate your learning and onboarding experience here at BlackRock.


Guidance on AI use for candidates


At BlackRock, AI has long been part of how we work - enhancing decision-making, improving operations, and helping us deliver better outcomes for clients. We encourage candidates to use AI thoughtfully to learn, prepare, and work more effectively; but during our interview process, we want to focus on getting to know you through your own experiences, thinking, and judgment. To support you, we've provided guidanceon when and how to use AI during our hiring process so you can approach each step with confidence and showcase your best self.


About BlackRock


At BlackRock, we are all connected by one mission: to help more and more people experience financial well-being. Our clients, and the people they serve, are saving for retirement, paying for their children's educations, buying homes and starting businesses. Their investments also help to strengthen the global economy: support businesses small and large; finance infrastructure projects that connect and power cities; and facilitate innovations that drive progress.


This mission would not be possible without our smartest investment - the one we make in our employees. It's why we're dedicated to creating an environment where our colleagues feel welcomed, valued and supported with networks, benefits and development opportunities to help them thrive.


To learn more about BlackRock, please visit Careers.BlackRock.com. We also encourage you to get to know us on LinkedIn, Instagram, YouTube, X, and TikTok.

BlackRock is proud to be an equal opportunity workplace. We are committed to equal employment opportunity to all applicants and existing employees, and we evaluate qualified applicants without regard to race, creed, color, national origin, sex (including pregnancy and gender identity/expression), sexual orientation, age, ancestry, physical or mental disability, marital status, political affiliation, religion, citizenship status, genetic information, veteran status, or any other basis protected under applicable federal, state, or local law.View theEEOC's Know Your Rights poster and its supplementand thepay transparency statement.

BlackRock is committed to full inclusion of all qualified individuals and to providing reasonable accommodations or job modifications for individuals with disabilities. If reasonable accommodation/adjustments are needed throughout the employment process, please email Disability.Assistance@blackrock.com. All requests are treated in line with ourprivacy policy.

BlackRock will consider for employment qualified applicants with arrest or conviction records in a manner consistent with the requirements of the law, including any applicable fair chance law.

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