ZipRecruiter

Log In

1

Drug Safety Scientist Jobs (NOW HIRING)

GRIFOLS, S.A.

Drug Safety Scientist

Clayton, NC · On-site

They will be responsible for providing oversight to Drug Safety Coordinators and the case intake ... Requirements: * BS in health science field, Pharmacy, CRA, biomedical sciences with 2 years of ...

Grifols

Drug Safety Scientist

Clayton, CA · On-site

They will be responsible for providing oversight to Drug Safety Coordinators and the case intake ... Requirements: * BS in health science field, Pharmacy, CRA, biomedical sciences with 2 years of ...

Viridian Therapeutics, Inc.

Safety Scientist

Waltham, MA · On-site +1

$127K - $155K/yr

The Safety Scientist collaborates primarily with the Product Safety Lead/Safety Physician for ... Knowledge of MedDRA and WHO Drug Dictionary terminology and its application as well as experience ...

Viking Therapeutics

Drug Safety Associate

San Diego, CA · On-site

$77K - $90K/yr

The Drug Safety Associate provides operational and documentation support for the company's clinical ... BA degree in Nursing, Pharmacy, Public Health, Biomedical Sciences, Life Sciences, or a related ...

Argenx

Safety Scientist

The safety scientist directs a cross functional team comprised of and Medical Safety, Clinical ... Experience with MedDRA, WHO Drug Dictionary * Understanding of the principles of databases ...

Systimmune

Drug Safety Physician

Princeton, NJ · On-site

$150K - $250K/yr

... of drug safety and pharmacovigilance regulations, pharmacovigilance practices, safety surveillance ... Collaborate with Medical Monitors and Clinical Research Scientists and vendor clinical staff as ...

next page

Showing results 1-20

All JobsDrug Safety Scientist Jobs

Drug Safety Scientist information

See salary details

$30

$61

$92

How much do drug safety scientist jobs pay per hour?

As of Aug 3, 2026, the average hourly pay for drug safety scientist in the United States is $61.42, according to ZipRecruiter salary data. Most workers in this role earn between $42.55 and $73.80 per hour, depending on experience, location, and employer.

What are common daily responsibilities for a Drug Safety Scientist, and how do they contribute to the overall drug development process?

As a Drug Safety Scientist, your typical day may involve reviewing and analyzing adverse event reports, preparing safety summaries, and ensuring timely compliance with regulatory requirements. You’ll frequently collaborate with clinical teams, regulatory affairs, and medical experts to evaluate safety signals and implement risk mitigation strategies. Your work is vital in monitoring and improving the safety profiles of medications throughout their lifecycle, thus directly supporting patient safety and effective drug development. Being detail-oriented and effectively communicating findings within cross-functional teams are key aspects of success in this role.

What is a Drug Safety Scientist job?

A Drug Safety Scientist is responsible for monitoring, evaluating, and ensuring the safety of pharmaceutical products throughout their lifecycle. They analyze adverse event data, assess potential risks, and collaborate with regulatory authorities to ensure compliance with safety regulations. Their role involves reviewing clinical trial data, post-market surveillance, and contributing to risk management strategies. By identifying and mitigating drug-related risks, they help ensure patient safety and regulatory adherence.

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

To thrive as a Drug Safety Scientist, you need a strong background in pharmacovigilance, life sciences, and data analysis, typically supported by a relevant degree such as pharmacology or pharmacy. Familiarity with safety databases (e.g., Argus, ARISg), regulatory guidelines (ICH, FDA), and certifications like the Drug Safety Certification are highly valuable. Strong attention to detail, analytical thinking, and effective communication skills are essential soft skills in this role. These skills and qualities are vital for assessing drug safety data, maintaining regulatory compliance, and effectively collaborating with internal and external stakeholders.

More about Drug Safety Scientist jobs
What cities are hiring for Drug Safety Scientist jobs? Cities with the most Drug Safety Scientist job openings:
What are the most commonly searched types of Drug Safety Scientist jobs? The most popular types of Drug Safety Scientist jobs are:
Who are the top companies hiring for Drug Safety Scientist jobs? The top employers for Drug Safety Scientist jobs are:
What states have the most Drug Safety Scientist jobs? States with the most job openings for Drug Safety Scientist jobs include:
What job categories do people searching Drug Safety Scientist jobs look for? The top searched job categories for Drug Safety Scientist jobs are:
What are popular job titles related to Drug Safety Scientist jobs? For Drug Safety Scientist jobs, the most frequently searched job titles are:
Drug Safety Scientist jobs near you
Infographic showing various Drug Safety Scientist job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $127,745 per year, or $61.4 per hour.

Drug Safety Scientist

Integrated Resources INC

Rockland, MA

Full-time

Re-posted 29 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

To utilize medical knowledge and operational expertise to ensure patient safety by performing medical assessment of adverse events, assembling up-front safety information, collecting quality follow-up and ensuring medical information is included in cases for investigational and marketed products. To facilitate operational integration and alignment with US Drug Safety Medicine and providing training to US Drug Safety on relevant activities.

Qualifications

- Provide initial medical evaluation of adverse events on company investigational and marketed products by determining the seriousness, expectedness, and therefore reportability of adverse events in line with FDA and global regulatory guidelines.
- Collect high quality medical follow-up information for serious cases.
- Perform quality review of clinical trial cases and develop queries as appropriate.
- Perform quality review of post-marketing serious adverse event reports as applicable.
- Perform initial assessment of non-adverse events to evaluate validity of report and identify requisite follow up.
- Log onto USDS phone line to receive incoming calls of potential adverse event reports and document information according to approved standards.
- Determine reportability including assessment of labeling for clinical trial and post-marketing cases processed by Global Drug Safety and distributed to US Drug Safety for potential reporting.
- Determine if adverse events should be reported to other manufacturers as required.
- Coordinate development of periodic safety reports and contribute to the development of aggregate reports as requested by US Drug Safety Medicine.
- Support Product Lead in signal detection activities as assigned.
- Participate in the set-up and approval of local clinical trials by developing drug safety manuals and SAE reconciliation plans, and conducting CRF reviews, and collaborating with US Drug Safety Medicine and GDS for the development and execution of Clinical Development plan as needed.
- Collaborate with GDS Staff to ensure a consistent global approach to safety by participating in meetings and implementing global standards within the department.
- Work closely with Medical Directors and Associate Medical Directors to ensure alignment by providing operational expertise.
- Represent USDS Operations with respect to the safety aspects of investigational and marketed products with external groups and on select cross-functional teams as appropriate.
- Provide medical operations expertise and help develop relevant training content for the case processing group and external vendors.
- Participate in internal and external training programs, meetings, and conferences to continually improve and build a knowledge base of product safety and risk management.
- Perform Sample QA per USDS and Company guidelines in order to identify quality trends and implement preventative actions.
- Obtain detailed knowledge of FDA and global safety regulations as applicable to assigned products and responsibilities.

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

View All Integrated Resources Jobs

Apply