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Temporary Drug Safety Scientist Jobs (NOW HIRING)

Freseniusglobal

Sr Drug Safety Scientist

Lake Zurich, IL · Hybrid

$133K - $146K/yr

Responsible for peer review in KabiSafe LSMV database and the Global Complaint Management Workflow (gCMW) for all Drug Safety Scientists and Data Specialists. Liaises with the Global Vigilance ...

Fresenius Kabi

Sr Drug Safety Scientist

Lake Zurich, IL · On-site

$133K - $146K/yr

Responsible for peer review in KabiSafe LSMV database and the Global Complaint Management Workflow (gCMW) for all Drug Safety Scientists and Data Specialists. Liaises with the Global Vigilance ...

Belcan

Drug Safety Coordinator

Clayton, NC · On-site

$19.23 - $26/hr

Assists Drug Safety Scientist (DSS) and management in building team environment among assigned ... We offer excellent opportunities for contract, temporary, temp-to-hire, and direct assignments. We ...

Socket.dev

Senior Safety Scientist I

Redwood City, CA · On-site

$120 - $150/hr

The Senior Safety Scientist within Global Patient Safety Science is an individual contributor who ... Acquire and contribute knowledge of relevant drug class and/or competitor safety issues. * Identify ...

New

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 ...

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 ...

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How much do temporary drug safety scientist jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for temporary 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 does a temporary drug safety scientist do?

A Temporary Drug Safety Scientist is responsible for monitoring and evaluating the safety of pharmaceutical products during clinical trials and after they reach the market. They review adverse event reports, analyze safety data, and ensure compliance with regulatory requirements. Their work helps to identify potential risks associated with medications, contributing to patient safety. As a temporary role, assignments may be project-based or for a fixed duration, supporting ongoing drug safety operations.

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

To thrive as a Temporary Drug Safety Scientist, you need a background in life sciences or pharmacy, knowledge of pharmacovigilance practices, and familiarity with regulatory requirements. Proficiency with drug safety databases (such as Argus or ARISg), MedDRA coding, and adverse event reporting systems is crucial. Strong attention to detail, analytical thinking, and effective communication skills help you interpret data and work with cross-functional teams. These competencies ensure accurate safety assessments and compliance with global regulations, which are vital for patient safety and successful product development.

What are some common challenges faced by temporary drug safety scientists, and how can they be managed effectively?

Temporary Drug Safety Scientists often encounter challenges such as quickly adapting to new processes, managing high volumes of safety data, and ensuring compliance with strict regulatory timelines. Since contracts are typically short-term, effective onboarding and proactive communication with permanent team members are crucial. Building strong organizational skills and familiarizing oneself with the company's pharmacovigilance systems early on can help manage workload and contribute to the team's success.

What cities are hiring for Temporary Drug Safety Scientist jobs?

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Temporary Drug Safety Scientist jobs near you

Drug Safety Scientist

Integrated Resources INC

Rockland, MA

Full-time

Re-posted 15 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

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