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Drug Safety Assistant Jobs (NOW HIRING)

Global Pharmatek

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 ...

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 ...

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 ... * Assist with implementation and documentation of CAPAs related to safety processes. * Prepare ...

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How much do drug safety assistant jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for drug safety assistant 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 a drug safety assistant?

Drug Safety Assistants are professionals who support pharmacovigilance teams by managing and processing reports of adverse drug reactions and other safety-related information. They help ensure that all data regarding the safety of pharmaceutical products is documented, evaluated, and reported in compliance with regulatory requirements. Their duties often include data entry, preparing safety reports, supporting audits, and communicating with healthcare professionals or patients as needed. Drug Safety Assistants play a crucial role in maintaining the safety profile of medicines and protecting public health.

What are some typical challenges faced by a drug safety assistant when processing adverse event reports?

Drug Safety Assistants often encounter challenges such as ensuring the accuracy and completeness of adverse event data, managing tight reporting deadlines, and coordinating with multiple stakeholders including healthcare professionals and regulatory authorities. Attention to detail is crucial, as incomplete or incorrect information can delay case processing and impact regulatory compliance. Additionally, navigating various data management systems and adapting to changing regulations can require continuous learning and flexibility.

What are the key skills and qualifications needed to thrive as a drug safety assistant, and why are they important?

To thrive as a Drug Safety Assistant, you need a solid understanding of pharmacovigilance processes, attention to detail, and typically a background in life sciences or a related field. Familiarity with drug safety databases (such as Argus or ARISg), regulatory reporting systems, and Good Pharmacovigilance Practices (GVP) is essential. Strong organizational skills, effective communication, and the ability to work well in teams are important soft skills for managing case data and reporting deadlines. These competencies ensure accurate adverse event reporting and compliance with regulatory standards, which are critical for patient safety and organizational reputation.

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Drug Safety Assistant jobs near you
Infographic showing various Drug Safety Assistant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 16% Part Time, 1% Contract, and 1% Nights. Highlights an 98% Physical, and 2% Remote job distribution, with an average salary of $53,254 per year, or $25.6 per hour.

Drug Safety Assistant

NJ • On-site

Global Pharmatek
Recruiting and Staffing Services • 51 - 200 employees
Learn more about Global Pharmatekexternal

Contractor

Re-posted 15 days ago

Job description

Company Description

We are proud to be part of the most precious thing on Earth: human life. Applying the technological expertise to the medical knowledge to derive near infallible results comes naturally to Global Pharma Tek, LLC. Global Pharma Tek is a fast-growing premier global pharmaceutical company that provides end-to-end services in pharmaceutical industry round the globe. Global Pharma Tek offers services like Drug Discovery, Clinical Trials, Drug Delivery, Regulatory and Intellectual Property Rights, Marketing and Strategic Human Resourcing. Global Pharma Tek is specialized in providing highly technical pharmaceutical and healthcare solutions and services in a cost effective way around the globe.

We are enterprise-class clinical software and clinical functional services provider, offers unique blend of both clinical trial domain and core IT expertise with thorough understanding of healthcare and pharma industry and regulatory standards. Global Pharma Tek, clinical functional services practice (FSP) enable pharmaceutical and life sciences industry customers realize their vision of safe, effective, and FDA approved delivery of drug at the lowest cost and at the fastest time to market. 

With core technology focus in the areas of statistical programming, business intelligence & data warehousing, enterprise application integration and enterprise architecture development, enterprise resource planning and custom applications development, along with clinical domain expertise, Global Pharma Tek offers a full range of specialized functional clinical & IT in-sourcing, IT projects development, clinical functional & IT projects outsourcing, software enabled services.

Job Description

Enter applicable information into the global safety database for initial or follow up cases received via paper, fax or email. Book-in, quality check and initially assess cases from suppliers sending cases to DSS via paper, email or fax.

Accept E2B cases received through the Argus Electronic Submissions Module (ESM) from European Health Authorities on behalf of Pharmaceutical Country Offices that are not online with Argus and other submitters as necessary.

Monitor electronic mailboxes and Argus ESM to ensure timely acceptance of Adverse Event (AE) Reports Perform data entry into databases, as needed.

Ensure proper coding of events and drugs for cases to ensure correct forwarding to the relevant Therapeutic Area Teams and Licensing Group.

Upload AE reports to the Drop in Data Entry II application on behalf of country offices cannot on their own. -----

Qualifications

Duration: one (1) year in length. Argus experience preferred. ----- BA degree required with 1-3 years of Safety/Pharamacoviliance Data experience. Argus experience. No Travel and No overtime. This is a 1 year Assignment.

Additional Information
All your information will be kept confidential according to EEO guidelines.
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About Global Pharmatek

Sourced by ZipRecruiter

Global Pharmatek is a leading Contract Research Organization (CRO) and integrated drug discovery solutions provider in the pharmaceutical industry. The company is located in Edison, New Jersey, USA. Their comprehensive range of services includes Drug Discovery, Clinical Trials, Regulatory Affairs, and Biometrics, designed with the goal of swiftly translating scientific innovation into a novel product. Founded with an unwavering commitment to enhance health and well-being worldwide, this leading-edge company lays emphasis on the highest quality standards, efficient delivery, and transparency.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

2011

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