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Data Annotation Education So Jobs (NOW HIRING)

Skild AI

Computer Vision AI & ML Engineer

San Mateo, CA · On-site

$127K - $149K/yr

Relevant industry experience is important, but ultimately less so than your demonstrated abilities ... Experience with data annotation tools, dataset management, and augmentation techniques.

Sigma Group

Tamil Translator (Remote) | Sigma AI

$45K - $58K/yr

Sigma is a leading global technology company specializing in data collection and annotation for ... If so, we'd love to hear from you! • Requirements We are looking for candidates with the ...

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Data Annotation Education So information

What is the difference between Data Annotation Education So vs Data Labeler?

AspectData Annotation Education SoData Labeler
Required CredentialsTypically requires training in annotation tools and basic data handlingUsually requires minimal formal education, focus on task-specific instructions
Work EnvironmentOften in training or educational settings, sometimes remotePrimarily in data labeling tasks, often remote or on-site
Industry UsageUsed in educational programs, training for data annotation rolesCommonly employed in data annotation and machine learning projects

Data Annotation Education So focuses on training individuals in data annotation techniques, often within educational or training contexts. In contrast, Data Labeler is a role that involves performing data labeling tasks in real-world projects. While both roles involve data annotation, the former emphasizes education and skill development, whereas the latter is about executing labeling tasks for AI and machine learning models.

Infographic showing various Data Annotation Education So job openings in the United States as of May 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 50% In-person, and 50% Remote job distribution.

Scientific Director - Commercial MedEd (Oncology)

The Lockwood Group, LLC

Remote

Full-time

Posted 26 days ago

Job description

This position can be based remotely (working from home) or at our headquarters in Stamford, CT.
About Lockwood: Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to identify effective, holistic, science-based strategies to address their objectives through medical communications. Our clients count on us to challenge their assumptions and help them creatively navigate around obstacles. From strategy through execution, we focus on accuracy, transparency, and scientific value to create programs that are evidence-based, clinically relevant, and contribute to the development of our clients' brands. Over a third of our staff hold advanced scientific or medical degrees, and most work from where they live. Because our flexible structure provides better work-life balance, we attract the best talent, facilitate their best work, and as a result, are more responsive to our clients, wherever and whenever they do business.
Summary: In this role, the Scientific Director is responsible for the planning, development, and oversight of scientific content for an assigned account or accounts across various therapeutic areas including Rare Disease addressing different target audiences.
Responsibilities: Responsibilities include working with the Group Scientific Director to provide clients with strategic medical communication recommendations that support the achievement of brand goals, independently leading execution of content development activities, supervising Associate Scientific Directors, and liaising with other in-house or freelance staff to manage writing and other content-related tasks such as conducting background research, data-checking, and reference annotation.
Education: An advanced degree in science is required.
Professional Skills & Experience:
  • Candidates must have 5 or more years of relevant job experience with promotional medical education content such as advisory boards, speaker programs, slide decks, etc.
  • This role requires demonstrated organizational, analytical, and interpersonal communication skills, as well as the ability to analyze and interpret scientific data, multitask, work independently, and manage projects within tight deadlines with limited direction.
  • Experience with established professional medical editorial processes (eg, AMA style) and ethical guidelines is also required.
  • Experience with Oncology / Multiple Myeloma / Hematologic Malignancy preferred.

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