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Pharmacovigilance Data Entry Jobs (NOW HIRING)

Amergis Healthcare Staffing

Clinic Office Manager

Newton, MA · On-site

$25.25 - $33/hr

Experience with EMR (electronic medical records), medical terminology and a basic understanding of clinical pharmacology * Data entry skills * Experience working with patients who are suffering from ...

New

Pioneer Data

Drug Safety Associate

Parsippany, NJ · On-site

... for data entry conventions, and for search functions in the safety database. Determine ... pharmacovigilance and/or data management preferred but not required. Experience and skill with ...

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How much do pharmacovigilance data entry jobs pay per hour?

As of Aug 21, 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 states have the most Pharmacovigilance Data Entry jobs?

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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 83% Full Time, and 17% Contract. Highlights an 92% In-person, and 8% Remote job distribution, with an average salary of $78,849 per year, or $37.9 per hour.

Senior Pharmacovigilance System Architect (Argus Administrator) - US

MMS Holdings Inc

Phoenix, AZ • On-site

$120 - $180/hr

Other

Posted 3 days ago

New

Job description

Senior Pharmacovigilance System Architect Roles & Responsibilities
  • Serves as Database Administrator for Argus Safety, including database configuration, issue resolution, maintenance, governance and daily support.
  • Performs installations, upgrades, configuration of reporting rules, and E2B reporting via gateway technologies (including set-up and configuration of Axway Gateway Interchange).
  • Provides support for all systems associated with PV and drug safety.
  • Performs updates to Argus configuration and processes as per changing EudraVigilance regulations.
  • Provides support and execution of activities related to EudraVigilancetesting for various clients.
  • Performs case migration/database transfers, file importing and supports other case processing activities.
  • Provides leadership in executing Argus upgrades and related activities.
  • Provides administrator support for other safety databases (such as ARISg).
  • Performs periodic coding dictionary (MedDRA & WHO drug) updates for Argus.
  • Provides technical assistance and support to Drug Safety Associate team with electronic submissions of serious adverse advents to European agencies.
  • Writes procedural documents including Standard Operating Procedures (SOP), Work Practice Documents, and Data Entry Manuals for Argus Safety.
  • Generates case processing metrics, reviews and makes suggestions and supports process improvement implementation.
  • Maintains technical expertise of regulatory requirements and ensures alignment with company working practices.
  • Assists with business development and capabilities efforts as needed.
  • Interacts directly and independently with client to coordinate all facets of projects; competent communicator, supports client capabilities as PV/drug safety systems SME.
  • Strong understanding and experience working with Argus configuration and study set up.
  • Strong understanding of global case processing and SAE reporting.
  • Strong understanding of global clinical trial development and data.
Requirements
  • College graduate Information Technology discipline or related field, or relevant experience.
  • Minimum of 5 years’ experience in Information Technology or similar field required.
  • Expert knowledge of scientific principles and concepts.
  • Reputation as emerging leader in field with sustained performance and accomplishment.
  • Proficiency with MS Office applications.
  • Hands‑on experience with clinical trial and pharmaceutical development preferred.
  • Good communication skills and willingness to work with others to clearly understand needs and solve problems.
  • Excellent problem-solving skills.
  • Good organizational and communication skills.
  • Familiarity with current ISO 9001 and ISO 27001 standards preferred.
  • Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
  • Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.
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