ZipRecruiter

Log In

1

Drug Safety Jobs (NOW HIRING)

Global Pharmatek

Drug Safety Assistant

Piscataway, NJ · On-site

Global Pharma Tek offers services like Drug Discovery, Clinical Trials, Drug Delivery, Regulatory ... Enter applicable information into the global safety database for initial or follow up cases ...

OSI Pharmaceuticals

Drug Safety Associate

Boulder, CO · On-site

The Safety Associate works fairly independently in receiving and reviewing serious adverse event (SAE) reports for completeness, performing initial triage, data entry into the Safety database and ...

Crispr Therapeutics

Senior Manager, Drug Safety

Boston, MA · On-site

$140K - $155K/yr

Train drug safety teams on established procedures and oversee compliance * Serve as the subject matter expert for ICSR intake processes and regulatory expectations, including presentations for ...

Biogen

Sr Associate II, Drug Safety

Cambridge, MA · On-site

$106K - $138K/yr

The Sr Associate II, Drug Safety is accountable for the end-to-end operational management of Adverse Events of Special Interest (AESIs) across the product lifecycle, including both Clinical Trial and ...

next page

Showing results 1-20

People also search for

All JobsDrug Safety Jobs

Drug Safety information

See salary details

$11

$25

$37

How much do drug safety jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for drug safety 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 is drug safety?

Drug safety, also known as pharmacovigilance, is the science and activities related to detecting, assessing, understanding, and preventing adverse effects or other drug-related problems. Professionals in drug safety monitor the safety profiles of medications, collect and analyze data on side effects, and help ensure that medicines are used safely and effectively. Their work is crucial for protecting public health and supporting regulatory compliance throughout a drug’s lifecycle.

What is the difference between Drug Safety vs Pharmacovigilance Specialist?

AspectDrug SafetyPharmacovigilance Specialist
Required CredentialsDegree in pharmacy, medicine, or life sciences; certifications like Drug Safety CertificationSimilar credentials; often the same certifications are required
Work EnvironmentPharmaceutical companies, CROs, regulatory agenciesSame as Drug Safety, often within the same teams
Industry UsageFocuses on monitoring and reporting adverse drug reactionsFocuses on detecting, assessing, and preventing adverse effects
Search & Comparison IntentOften compared for roles in drug safety monitoringSimilar roles, but with a focus on safety data analysis

Drug Safety and Pharmacovigilance Specialist roles are closely related, often overlapping in responsibilities and required qualifications. Both work within the pharmaceutical industry to ensure medication safety, but Drug Safety may emphasize reporting adverse events, while Pharmacovigilance focuses on analyzing safety data to prevent issues.

What are some common challenges faced by professionals in Drug Safety roles, and how can they be managed?

Professionals in Drug Safety often face challenges such as staying current with evolving regulatory requirements, managing large volumes of adverse event data, and ensuring timely reporting to health authorities. These challenges can be managed through continuous training, strong collaboration with cross-functional teams (such as clinical, regulatory, and medical affairs), and leveraging specialized safety databases and software. Additionally, clear communication and robust standard operating procedures help maintain compliance and data integrity in this dynamic work environment.

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

To thrive in Drug Safety, a strong background in life sciences, pharmacovigilance principles, and regulatory guidelines is essential, often supported by a relevant degree such as pharmacy, nursing, or life sciences. Familiarity with safety databases (like Argus or ARISg), MedDRA coding, and certifications such as RAPS or DIA are commonly required. Attention to detail, analytical thinking, and clear communication skills help professionals accurately evaluate data and collaborate across teams. These competencies are crucial for ensuring patient safety, regulatory compliance, and effective risk management throughout the drug lifecycle.
More about Drug Safety jobs
What cities are hiring for Drug Safety jobs? Cities with the most Drug Safety job openings:
What are the most commonly searched types of Drug Safety jobs? The most popular types of Drug Safety jobs are:
What states have the most Drug Safety jobs? States with the most job openings for Drug Safety jobs include:
What job categories do people searching Drug Safety jobs look for? The top searched job categories for Drug Safety jobs are:
Drug Safety jobs near you
Infographic showing various Drug Safety job openings in the United States as of June 2026, with employment types broken down into 80% Full Time, 19% Part Time, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $53,254 per year, or $25.6 per hour.

Drug Safety Operations Associate

The Rockridge Group

Stamford, CT

Full-time

Posted 14 days ago

Job description

TITLE: Drug Safety Operations Associate
LOCATION: Stamford, CT
DURATION: 12 months
Job Description:
  • Position performs adverse event processing and submission responsibilities supporting the Case Management function within Drug Safety Operations.
Primary Responsibilities
  • Perform case processing activities (triage, data entry, report distribution) as required
    • Assess, process, and data enter all AE case types to meet compliance requirements
    • Perform triage on all case types to determine prioritization (if requested by Purdue)
    • Identify adverse events, seriousness, and listed Ness / labeled Ness for case assessment; review additional incoming information to determine reportability
    • Select the appropriate as reported causality and company causality
    • Perform all appropriate coding using MedDRA, WHO-DRUG, and Company Product dictionaries.
    • Own case narrative - create narrative text as required for medical orientation
    • Determine follow-up requirements and request follow-up as appropriate (e-mail, phone call, letter, etc.) to request additional information
    • Support ICSR submissions and transmissions as needed.
    • Perform CRO case QC activities, reconciliation etc as required.
    • Work on highest priority or assigned cases using Workflow Management System, or as directed
    • Participate in inspections and audits as identified, including interviews and provision of requested data
    • Meet KPIs/KQIs as designated by Purdue and in compliance with company guidelines and policies
    • Assist in writing late ICSR related deviations and CAPAs, upon request
    • Perform additional tasks as assigned. Work independently, assess matters, propose resolutions, and appropriately escalate internally within Purdue organization
Education and Experience Requirements:
  • Bachelor’s degree (advanced degree preferred) in life science or healthcare (e.g. nursing, pharmacy)
  • Five (5+) years of experience in a pharmaceutical/biopharmaceutical company
  • Three (3+) years in Drug Safety Operations role;
  • Experience overseeing CRO teams of case processors preferred
  • US FDA pharmacovigilance inspection experience preferred
Necessary Knowledge, Skills, and Abilities:
  • Resource and workflow management (monitoring and assigning tasks)
  • Up-to-date knowledge of US and international PV regulations and best practices
  • MedDRA coding
  • Considers present and future impacts when making recommendations
  • Strong negotiation and problem-solving skills
  • Analytical skills and attention to detail
  • Accountability – takes ownership of deliverables
Necessary Knowledge, Skills, and Abilities:
  • Resource and workflow management (monitoring and assigning tasks)
  • Up-to-date knowledge of US and international PV regulations and best practices
  • MedDRA coding
  • Considers present and future impacts when making recommendations
  • Strong negotiation and problem-solving skills
  • Analytical skills and attention to detail
  • Accountability – takes ownership of deliverables