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As of Aug 5, 2026, the average hourly pay for current argus in the United States is $49.14, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $55.53 per hour, depending on experience, location, and employer.

What is the Current Argus?

The Current Argus is a newspaper based in Carlsbad, New Mexico, that covers local news, sports, business, entertainment, and community events. It serves Carlsbad and the surrounding areas, providing both print and digital news coverage. The publication is known for its in-depth reporting on local issues and its commitment to informing and engaging the community.

What are the typical responsibilities of a journalist at the Current Argus?

Journalists at local newspapers such as the Current Argus are often responsible for researching, interviewing, and writing stories on a variety of community topics, including local government, education, and events. They may be expected to cover breaking news, attend public meetings, and maintain relationships with sources to stay informed about issues impacting the community. Collaboration with editors, photographers, and other reporters is common to ensure stories are accurate, timely, and engaging. Additionally, journalists often work under tight deadlines and may be required to manage multiple assignments simultaneously.

What are the key skills and qualifications needed to thrive as a journalist at the Current Argus?

To thrive as a journalist, you need strong writing, research, and investigative skills, typically supported by a degree in journalism or communications. Familiarity with content management systems, digital publishing tools, and multimedia editing software is often required. Excellent communication, curiosity, and adaptability are crucial soft skills for telling compelling stories and engaging with diverse sources. These abilities ensure accurate, timely, and impactful news coverage that meets the needs of the publication and its audience.
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Infographic showing various Current Argus job openings in the United States as of July 2026, with employment types broken down into 34% Locum Tenens, 9% Full Time, 54% Nights, and 3% Summer. Highlights an 88% Physical, 5% Hybrid, and 7% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

Senior Pharmacovigilance System Architect (Argus Administrator) - US

MMS

Raleigh, NC • On-site

Full-time

Posted 20 days ago

Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.

Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.

Senior Pharmacovigilance System Architect

We are recruiting for an experienced Pharmacovigilance System Architect (Argus Administrator SME) to join our US team.

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 EudraVigilance testing 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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About M. M. S.

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

Los Angeles, CA, US

Year founded

1980

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