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Drug Safety Manager Jobs (NOW HIRING)

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Drug Safety Manager information

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$37K

$86K

$136.5K

How much do drug safety manager jobs pay per year?

As of Aug 7, 2026, the average yearly pay for drug safety manager in the United States is $85,971.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,500.00 and $102,500.00 per year, depending on experience, location, and employer.

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

AspectDrug Safety ManagerPharmacovigilance Specialist
CredentialsTypically requires a degree in pharmacy, life sciences, or related field; certifications like PV or REMS are commonSimilar educational background; often holds certifications in pharmacovigilance or drug safety
Work EnvironmentLeads drug safety teams, manages safety data, and oversees compliance within pharmaceutical companiesFocuses on collecting, analyzing, and reporting safety data, often working under supervision
Industry UsageUsed in pharmaceutical and biotech companies for overseeing safety programsCommonly used in regulatory agencies and contract research organizations

While both roles involve drug safety and require similar qualifications, the Drug Safety Manager typically has a leadership role overseeing safety operations, whereas the Pharmacovigilance Specialist focuses on data collection and analysis. The manager has broader responsibilities, including team management and strategic planning.

What are the key skills and qualifications needed to thrive as a drug safety manager?

To thrive as a Drug Safety Manager, you need expertise in pharmacovigilance, regulatory compliance, and drug safety reporting, typically backed by a degree in pharmacy, life sciences, or a related field. Familiarity with safety databases (such as Argus or ARISg), MedDRA coding, and ICH-GCP guidelines is commonly required, along with relevant certifications like those from the Drug Information Association (DIA). Strong analytical thinking, attention to detail, and effective communication skills are crucial for managing safety data and collaborating with cross-functional teams. These skills ensure accurate safety monitoring, regulatory adherence, and the protection of patient well-being throughout a drug’s lifecycle.

What are the main challenges drug safety managers face when ensuring compliance with global pharmacovigilance regulations?

Drug Safety Managers often navigate complex and evolving international regulations to ensure a company's pharmacovigilance practices are compliant. They must coordinate with cross-functional teams to gather timely and accurate safety data, manage case processing workflows, and prepare regulatory submissions under strict deadlines. Staying updated on changing global requirements and aligning internal processes accordingly can be challenging, but is crucial for patient safety and product success. Effective communication, attention to detail, and proactive risk management are key in overcoming these challenges.

What does a drug safety manager do?

A Drug Safety Manager is responsible for overseeing the collection, evaluation, and reporting of data related to the safety of pharmaceutical products. They ensure compliance with regulatory requirements and help identify, assess, and mitigate risks associated with medications. Their role often includes managing a team, developing safety protocols, and communicating findings to regulatory authorities and internal stakeholders. By maintaining vigilance over drug safety, they help protect patient health and support the ongoing improvement of pharmaceutical products.
More about Drug Safety Manager jobs
What cities are hiring for Drug Safety Manager jobs? Cities with the most Drug Safety Manager 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 Manager jobs? States with the most job openings for Drug Safety Manager jobs include:
Infographic showing various Drug Safety Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 18% Part Time, 2% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $85,971 per year, or $41.3 per hour.

Drug Safety Associate I

Integrated Resources INC

Horsham, PA • On-site

Contractor

Re-posted 11 days ago


Job description

Company Description

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

Job Description

Responsible for the receipt and data entry of adverse event reports following company standard operating procedures, internal business practices and regulatory guidance documents, to ensure compliance with worldwide safety regulations and corporate policies.
PRINCIPAL RESPONSIBILITIES:
Case processing: 95%
Definition: The completion of full case information on the database, including quality review to ensure accuracy and completeness
Activities Include:
May Triage and classify ICSRs for report type, seriousness, causality, expectedness/labeling and reporting; prioritize ICSR according to regulatory requirements
Confirmation of Safety Coordinator case registry data
Database searches as necessary
Completion of remaining case data entry, including narrative or auto-narrative
Completion of risk and quality (label, approval, manual coding and quality review steps).
Clarification of unclear or illegible information from the LSO or Call Centre
Discussion of source documents, coding conventions and ad-hoc queries with Pharmacovigilance Physician
Request deletions as necessary
Single case unblinding
Processes & Procedures:
Definition: Continuing awareness of company procedures and guidelines to maintain regulatory compliance
Activities Include:
Standard Operating Procedures and Working Instructions
Department guidance documents
MedDRA coding dictionary and MedDRA Points to Consider
Understand relevant safety implications regarding contracts with operating companies and/or marketing partners
DECISION-MAKING AND PROBLEM-SOLVING:
Application and knowledge of Departmental processes and guidelines, regulations and regulatory guidelines, contractual arrangements, product specific information and database/systems functionality to individual case processing and evaluation. Communicate questions clearly and concisely to the appropriate audience and accompany with possible solutions.
REPORTING RELATIONSHIPS: Describe where this position fits in relation to the rest of the department it resides.
Supervised by Senior DSA
WORKING RELATIONSHIPS/INTERFACES: Describe the primary working relationships (internal & external) and primary interfaces along with the frequency and purpose/nature.
Global Medical Safety Operations (GMSO) is a functional area within the Global Medical Organization (GMO)
All others in GMSO
Medical Affairs
Clinical Affairs
Contract Research Organizations
Local Safety Officers
Marketing Partners

Qualifications

EDUCATION & EXPERIENCE REQUIREMENTS: Describe the minimum knowledge, skill and ability requirements for the position. Include any degrees or certifications which are required and/or desirable.
Registered Nurse OR
Health/Biomedical Degree (BS, PhD or other related scientific degree/qualification) OR
Licensed Practical Nurse without Bachelors degree but with knowledge of Drug Safety usually exhibited by minimum 5 years experience in pharmaceutical safety-related role.
Pharmaceutical industry experience is preferred

Required Skills/Abilities
Intermediate Information Technology Skills
Data entry experience desired
Accountability for delivery of results
Decision making skills
Problem solving skills
Proactive approach/uses own initiative
Manages owe work, able to prioritize, plan and organize work assignments and work under strict timelines
Ability to follow guidelines, working practices etc. Experience of working with SOP/WI preferred
Quality oriented, with attention to detail/accuracy
Flexibility/Adaptability
Positive attitude
Good team player
Ability to work independently and to collaborate
Good written and verbal communication skills
Understanding of medical terminology
Ability to summarize medical information

Additional Information

Thanks!!
With Regards,
Sasha Sharma
Clinical Recruiter
Integrated Resources, Inc
IT REHAB CLINICAL NURSING
Direct: 732-662-7964 | (W) 732-549-2030 x 219

Inc. 5000 - 2007-2015 (9 Years in a row)


Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996