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Drug Safety Risk Management Jobs (NOW HIRING)

Job Summary The Director of Patient Safety and Risk Management will be responsible for the strategic oversight and implementation of an effective Patient Safety and Enterprise Risk Management program.

The Safety and Risk Management Consultant (Consultant) of TRISTAR's Risk Control Division, Aspen Risk Management Group (Aspen), provides safety, risk, and loss control consultation services to ...

... risk and quality (label, approval, manual coding & quality review steps) Clarification of unclear or illegible information from the LSO or Call Centre Discuss source documents, coding conventions and ...

Drug Safety Associate Duration: 12 months contract, extendable up to 36 months Location: Parsippany ... You may participate in the company group medical insurance plan Safety Data Management Specialist ...

Drug Safety Associate III

Alameda, CA · On-site

$124K - $177K/yr

Development of study specific safety management plan from Exelixis Drug Safety template Development ... review and update of drug safety forms and templates, and harmonization with relevant clinical ...

Drug Safety Associate III

Alameda, CA · On-site

$124K - $177K/yr

Development of study specific safety management plan from Exelixis Drug Safety template ... Development, review and update of drug safety forms and templates, and harmonization with relevant ...

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Drug Safety Risk Management information

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How much do drug safety risk management jobs pay per hour?

As of Jun 6, 2026, the average hourly pay for drug safety risk management in the United States is $25.60, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $28.61 per hour, depending on experience, location, and employer.

What are some common challenges faced by professionals in Drug Safety Risk Management, and how can they be addressed?

Professionals in Drug Safety Risk Management often face challenges such as staying current with evolving regulatory requirements, effectively analyzing large volumes of safety data, and ensuring clear communication with cross-functional teams. To address these, it's important to engage in continuous professional development, utilize advanced pharmacovigilance tools, and foster strong collaboration with regulatory, clinical, and medical affairs colleagues. Proactively managing these challenges helps ensure timely identification and mitigation of drug-related risks, ultimately promoting patient safety.

What are the key skills and qualifications needed to thrive in Drug Safety Risk Management, and why are they important?

To thrive in Drug Safety Risk Management, you need expertise in pharmacovigilance, risk assessment, regulatory guidelines, and often a degree in pharmacy, medicine, or life sciences. Familiarity with safety databases (like Argus or ARISg), MedDRA coding, and compliance with ICH and FDA regulations is crucial. Strong analytical thinking, attention to detail, and effective communication help professionals identify, evaluate, and mitigate drug-related risks. These skills ensure patient safety, regulatory compliance, and effective decision-making throughout the drug lifecycle.

What is drug safety risk management?

Drug safety risk management refers to the systematic process of identifying, evaluating, and minimizing the risks associated with pharmaceutical products throughout their lifecycle. Professionals in this field develop and implement risk management plans to ensure patient safety, monitor adverse events, and comply with regulatory requirements. Their work helps pharmaceutical companies and regulatory agencies prevent, detect, and address potential drug-related problems, ultimately protecting public health.

What is the difference between Drug Safety Risk Management vs Pharmacovigilance Specialist?

AspectDrug Safety Risk ManagementPharmacovigilance Specialist
CredentialsHealthcare background, certifications in drug safetyHealthcare or life sciences background, pharmacovigilance certifications
Work EnvironmentRegulatory agencies, pharmaceutical companies, clinical settingsPharmaceutical companies, CROs, regulatory agencies
Industry UsageFocuses on risk mitigation, safety monitoring, and complianceMonitoring, detecting, and reporting adverse drug reactions

Drug Safety Risk Management and Pharmacovigilance Specialist roles overlap in safety monitoring but differ in scope. Risk management emphasizes proactive strategies to minimize drug risks, while pharmacovigilance focuses on detecting and reporting adverse events. Both roles require similar credentials and work environments, often within pharmaceutical companies or regulatory bodies.

Director, Patient Safety & Risk Management

Full-time

Posted 23 days ago


Henry Mayo Newhall Hospital rating

7.1

Company rating: 7.1 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

432nd of 993 rated hospitals


Job description

Job Summary

The Director of Patient Safety and Risk Management will be responsible for the strategic oversight and implementation of an effective Patient Safety and Enterprise Risk Management program. The facility wide responsibilities for this integrated role will require proactive, strategic planning to ensure the alignment of critical functions that will promote a just culture, prioritize the HMNH zero harm goals and protect the organization from violations of the law, and/or regulatory risk. 

The Director will be responsible for the management of program personnel and fiscal and material resources. They will support staff development and continuous program and process improvement. They will be a role model for the Henry Mayo Way of patient, employee, partner and community engagement.

Licensure and Certification:

  • Clinical Licensure (RN, PharmD, Medical, or Healthcare related field) preferred
  • Certificate Professional in Patient Safety (CPPS) preferred 
  • Certified Professional in Healthcare Quality (CPHQ) preferred 
  • Certified Professional in Healthcare Risk Management (CPHRM) preferred

Education:

  •   Bachelor's degree required 
  • Master's degree in related field or Juris Doctor preferred

Experience:

  • Minimum five (5) years' experience in Healthcare Law, Risk Management and/or Patient Safety 
  • Minimum three (3) years' experience in management required 
  • Previous clinical care experience required

Knowledge and Skills:

  • Demonstrates and applies leadership and management theories, principles, practices, techniques and methods to create and maintain a high functioning, engaged team. 
  • Effective oral, written and presentation skills. 
  • Ability to interact and collaborate with all levels of the organization, including the Medical Staff 
  • Advocate and facilitator for continuous improvement
Employment Type: Full Time