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Map Annotation Jobs in Cranford, NJ (NOW HIRING)

Datavant

Clinical AI Data Specialist

New York, NY

The technical work -- annotation at scale, prompt and rule iteration, and label-quality analysis ... mapping to clinical ontologies (ICD-10-CM/PCS, CPT, RxNorm) when required by project scope

Wipro Limited

Driver Behavior Analyst

Manhattan, NY · On-site

$73K - $83K/yr

Behavioral Annotation: Analyze video and sensor data from US roads to label driver intent ... Business Analyst/ Data Analyst(Maps) . Experience: 3-5 Years . The expected compensation for this ...

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Map Annotation information

What are the key skills and qualifications needed to thrive in the Map Annotation position, and why are they important?

To thrive as a Map Annotation specialist, you should have excellent attention to detail, spatial reasoning abilities, and familiarity with geographic information systems (GIS) or digital mapping platforms. Proficiency with annotation tools like ArcGIS, QGIS, or proprietary annotation software is often required, and some roles may prefer prior experience or training in cartography or remote sensing. Strong communication, problem-solving skills, and the ability to follow complex guidelines are valuable soft skills in this position. These skills and qualities are vital because accuracy and consistency in annotating map data directly influence the quality of geographic datasets used in applications like navigation, autonomous vehicles, and urban planning.

What does a typical day look like for someone working in Map Annotation?

In a Map Annotation role, your day often involves reviewing and labeling satellite imagery or digital maps using specialized software to identify features like roads, buildings, or natural landmarks. You may work independently or as part of a team, following detailed guidelines to ensure consistency and high accuracy across the dataset. Collaboration with supervisors or quality assurance teams is common to resolve ambiguities and uphold annotation standards. The work is usually computer-based, and you might attend regular meetings to discuss updates to project requirements or annotation protocols. Over time, you can expand your responsibilities by training new teammates or moving into lead annotator or project coordinator roles.

What is a Map Annotation job?

A Map Annotation job involves labeling, tagging, or annotating geographic data to improve the accuracy of digital maps. This can include identifying roads, landmarks, businesses, addresses, and other points of interest. Annotators help train AI and mapping systems by reviewing and verifying location-based information. The role requires attention to detail, spatial awareness, and sometimes familiarity with local geography. These jobs are often remote and may be project-based.

What job categories do people searching Map Annotation jobs in Cranford, NJ look for? The top searched job categories for Map Annotation jobs in Cranford, NJ are:
What cities near Cranford, NJ are hiring for Map Annotation jobs? Cities near Cranford, NJ with the most Map Annotation job openings:
Map Annotation jobs near you
Infographic showing various Map Annotation job openings in Cranford, NJ as of June 2026, with employment types broken down into 68% Full Time, 10% Part Time, and 22% Contract. Highlights an 84% In-person, 7% Hybrid, and 9% Remote job distribution.
Senior Clinical Programmer - SDTM and R/SAS 3635027

Senior Clinical Programmer - SDTM and R/SAS 3635027

Axiom Path

Bridgewater, NJ • Remote

$75 - $80/hr

Full-time

Posted 11 days ago

Job description

Be Part Of A High-Performing Team:

Join a growing clinical programming function within a science-driven biopharmaceutical organization developing therapies for patients with serious and rare diseases. This newly established team is bringing critical SDTM programming capabilities in-house and works closely with data management, biostatistics, and statistical programming. The environment is collaborative, technically rigorous, and well suited to an experienced programmer who enjoys building reliable clinical-data solutions while helping shape new internal processes.

What's In Store For You:

Engagement: W2 only (no C2C/1099)

This is a fully remote, 12-month consulting assignment open to candidates located anywhere in the United States. Availability during Eastern Time business hours is preferred.

The role offers the opportunity to become one of the early members of a growing clinical programming team and contribute directly to the organization’s transition from outsourced SDTM programming to an internal delivery model. A contract extension may be possible based on performance and business needs, although permanent conversion is not currently planned.

How You Will Make An Impact:

  • Create production-quality SDTM datasets using both SAS and R.
  • Independently perform quality control and validation of SDTM datasets.
  • Develop dataset specifications using CDISC standards and current SDTM Implementation Guides.
  • Create annotated CRFs, including domain mappings, annotation boxes, controlled terminology, and page-level placement.
  • Apply existing team macros and programming utilities to support annotated CRF and SDTM production.
  • Develop SAS- and R-based listings and reports supporting medical monitoring, clinical data management, and statistical endpoint monitoring.
  • Perform clinical-data checks, reconciliations, and issue investigation as assigned.
  • Collaborate closely with data managers, biostatisticians, statistical programmers, and clinical-study stakeholders.
  • Help establish scalable internal standards, workflows, and quality practices as SDTM programming transitions in-house.
  • Manage multiple study deliverables independently while maintaining accuracy, traceability, and timely execution.

Do you bring proven success in SDTM programming with both SAS and R?

  • Approximately 8–10 years of hands-on clinical programming experience in pharmaceutical, biotechnology, CRO, or related regulated clinical environments.
  • Strong production programming proficiency in both SAS and R.
  • Demonstrated experience creating and independently quality-checking SDTM datasets.
  • Strong knowledge of CDISC standards and current SDTM Implementation Guides.
  • Hands-on experience creating annotated CRFs, including page-level annotations and terminology mapping.
  • Ability to use established macros, functions, and programming utilities.
  • Experience translating raw clinical data, CRFs, specifications, and programming standards into compliant SDTM deliverables.
  • Strong analytical, troubleshooting, documentation, and quality-control skills.
  • Ability to work independently as an individual contributor in a small and evolving team.
  • Strong written and verbal communication skills.
  • Experience with JReview is highly preferred.
  • Experience with Shiny, Pharmaverse, or R Markdown is highly desirable.
  • Exposure to SQL programming is preferred.
  • Experience supporting medical monitoring, data-management reports, reconciliations, or statistical endpoint monitoring is beneficial.

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