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Pharmacovigilance Data Entry Jobs (NOW HIRING)

Evolution Research Group

Data Entry Coordinator

Miami, FL · On-site

$18 - $22/hr

S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic ... As a Data Entry Coordinator, you will be responsible for the overall coordination, organization ...

Quotient Sciences

Data Entry Coordinator

Miami, FL · On-site

... pharmacology, clinical trials, and commercial product manufacturing. Our proprietary and disruptive platform - "Translational Pharmaceutics ® " - integrates Drug Product Manufacturing and Clinical ...

Global Pharmatek

NJ · On-site

Upload AE reports to the Drop in Data Entry II application on behalf of country offices cannot on their own. Qualifications BA degree required with 1-3 years of Safety/ Pharmacovigilance Data ...

Harrow Defunct

Data Entry Associate, QA

Data Entry Associate, QA Under the general guidance of the Quality Assurance Specialist, the Data ... Willingness to grow knowledge of pharmacovigilance principles and compliance expectations. Position ...

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How much do pharmacovigilance data entry jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for pharmacovigilance data entry in the United States is $37.91, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $51.92 per hour, depending on experience, location, and employer.

What is a pharmacovigilance data entry?

A Pharmacovigilance Data Entry job involves recording, managing, and maintaining drug safety data, primarily adverse event reports, in regulatory databases. Professionals in this role ensure accuracy, completeness, and compliance with industry regulations and company procedures. They work closely with pharmacovigilance teams to support drug safety monitoring and reporting. Attention to detail and knowledge of medical terminology are essential for this role.

What are the typical day-to-day responsibilities of a pharmacovigilance data entry professional?

As a Pharmacovigilance Data Entry professional, your daily tasks generally include entering adverse event data into safety databases, verifying the accuracy and completeness of reports, and assisting in data quality checks and coding medical terms according to regulatory standards. You may collaborate with safety associates, quality reviewers, and sometimes medical professionals to ensure data integrity and timely submissions. Additionally, you may support the preparation of documentation for regulatory filings or audits. The work environment is usually structured and process-driven, with an emphasis on accuracy and confidentiality. These responsibilities are fundamental to maintaining the integrity of pharmacovigilance processes and supporting overall drug safety efforts.

What are the key skills and qualifications needed to thrive in the pharmacovigilance data entry position, and why are they important?

To thrive as a Pharmacovigilance Data Entry professional, you need strong attention to detail, rapid and accurate data entry skills, and typically a background in life sciences or a related field. Familiarity with pharmacovigilance databases such as Argus Safety or MedDRA coding, as well as proficiency in Microsoft Office applications, is often required. Excellent organizational skills, reliability, and the ability to communicate effectively with cross-functional teams are critical soft skills for success in this role. These skills ensure that safety data is recorded swiftly and accurately, supporting effective drug safety monitoring and regulatory compliance.

Can pharmacovigilance data entry work from home?

Pharmacovigilance data entry roles are often suitable for remote work, as they primarily involve data input and review that can be performed using a computer and secure internet connection. Many companies offer work-from-home options for these positions, especially with the use of specialized data management tools and adherence to confidentiality protocols.

Is pharmacovigilance data entry a stressful job?

Pharmacovigilance data entry can be stressful due to the need for accuracy and attention to detail when managing large volumes of safety data. Deadlines and the importance of compliance with regulatory standards may also contribute to job pressure, but the work environment is typically structured to support precision and consistency. Proper training and experience can help manage stress levels in this role.
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What are the most commonly searched types of Pharmacovigilance Data Entry jobs?

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What states have the most Pharmacovigilance Data Entry jobs?

States with the most job openings for Pharmacovigilance Data Entry jobs include:

What job categories do people searching Pharmacovigilance Data Entry jobs look for?

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Pharmacovigilance Data Entry jobs near you
Infographic showing various Pharmacovigilance Data Entry job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $78,849 per year, or $37.9 per hour.

Drug Safety Data Management Specialist

Morris Plains, NJ • On-site

Artech Information System LLC
Recruiting and Staffing Services • 10K+ employees
Learn more about Artech Information System LLCexternal

Full-time

Re-posted 11 days ago

Job description

Company Description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

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 company's 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.
  • BA degree required with 1-3 years of Safety/Pharmacovigilance Data experience preferred.


Qualifications

BA degree required with 1-3 years of Safety/Pharmacovigilance Data experience preferred.



Additional Information

Sneha Shrivastava

Technical Recruiter (Clinical/Scientific)

 Artech Information Systems LLC

360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 

Office: 973.967.3348 | Fax: 973.998.2599

Connect with us on - LinkedIn | Facebook | Twitter



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About Artech

Sourced by ZipRecruiter

Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).

Industry

Recruiting and staffing services

Company size

10,000+ Employees

Headquarters location

Morristown, NJ, US

Year founded

1992

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