Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to ... freelance staff to manage writing and other content-related tasks such as conducting background ...
Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to ... freelance staff to manage writing and other content-related tasks such as conducting background ...
Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to ... freelance staff to manage writing and other content-related tasks such as conducting background ...
Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to ... freelance staff to manage writing and other content-related tasks such as conducting background ...
Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to ... freelance staff to manage writing and other content-related tasks such as conducting background ...
Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to ... freelance staff to manage writing and other content-related tasks such as conducting background ...
Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to ... freelance staff to manage writing and other content-related tasks such as conducting background ...
Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to ... freelance staff to manage writing and other content-related tasks such as conducting background ...
... about medical evidence? We're looking for a Principal Clinical Scientist to bring senior-level ... Prior involvement in data annotation, data quality assurance, or evaluation systems * Experience ...
... about medical evidence? We're looking for a Principal Clinical Scientist to bring senior-level ... Prior involvement in data annotation, data quality assurance, or evaluation systems * Experience ...
... medical evidence, regulatory submissions, and patient outcomes? We're looking for a Principal ... Prior experience with data annotation, data quality assurance, or evaluation systems * Familiarity ...
... medical evidence, regulatory submissions, and patient outcomes? We're looking for a Principal ... Prior experience with data annotation, data quality assurance, or evaluation systems * Familiarity ...
... with data annotation, data quality review, or AI evaluation workflows Background in ... medical affairs, or clinical operations Exposure to real‐world evidence (RWE) or post‐market ...
... with data annotation, data quality review, or AI evaluation workflows Background in ... medical affairs, or clinical operations Exposure to real‐world evidence (RWE) or post‐market ...
... medical evidence, regulatory submissions, and patient outcomes? We're looking for a Principal ... Prior experience with data annotation, data quality assurance, or evaluation systems * Familiarity ...
... medical evidence, regulatory submissions, and patient outcomes? We're looking for a Principal ... Prior experience with data annotation, data quality assurance, or evaluation systems * Familiarity ...
Senior Behavioral Health Consultant
San Francisco, CA · Remote
$150/hr
This is not therapy delivery, tutoring, or generic annotation work.About AlignedAt Aligned, we ... Unlike low-skill freelance work on traditional consulting platforms, our community of experts set ...
Senior Behavioral Health Consultant
San Francisco, CA · Remote
$150/hr
This is not therapy delivery, tutoring, or generic annotation work.About AlignedAt Aligned, we ... Unlike low-skill freelance work on traditional consulting platforms, our community of experts set ...
Product Manager, Pay and Safety -- Handshake AI
San Francisco, CA · On-site
$145K - $180K/yr
... freelance AI training gigs to first internships to full-time careers and beyond. This unique value ... Medical, dental, and vision, mental health support, $500 wellness stipend 📚 Growth: $2,000 ...
Quick apply
Product Manager, Pay and Safety -- Handshake AI
San Francisco, CA · On-site
$145K - $180K/yr
... freelance AI training gigs to first internships to full-time careers and beyond. This unique value ... Medical, dental, and vision, mental health support, $500 wellness stipend 📚 Growth: $2,000 ...
Freelance Medical Annotation information
See salary details
$23.52 is the 25th percentile. Wages below this are outliers.
$14.90 - $25.57
31% of jobs
The median wage is $32.14 / hr.
$25.57 - $36.23
31% of jobs
$36.23 - $46.90
4% of jobs
$56.23 is the 75th percentile. Wages above this are outliers.
$46.90 - $57.56
10% of jobs
$57.56 - $68.23
9% of jobs
$68.23 - $78.89
5% of jobs
$78.89 - $89.55
0% of jobs
$89.55 - $100.22
8% of jobs
$100.22 - $110.88
0% of jobs
$110.88 - $121.55
0% of jobs
$121.55 - $132.21
1% of jobs
$14
$47
$132
How much do freelance medical annotation jobs pay per hour?
What are the key skills and qualifications needed to thrive as a Freelance Medical Annotation Specialist, and why are they important?
What are some common challenges faced by freelance medical annotators, and how can they be managed effectively?
What is freelance medical annotation?
What is the difference between Freelance Medical Annotation vs Medical Data Labeler?
| Aspect | Freelance Medical Annotation | Medical Data Labeler |
|---|---|---|
| Credentials | Basic medical knowledge, attention to detail | Basic understanding of data labeling |
| Work Environment | Remote, freelance projects | Remote, often part of a team |
| Industry Usage | Healthcare, AI training, research | AI, machine learning, data processing |
| Search & Comparison Intent | Understanding freelance roles in medical AI | Comparing data labeling jobs in healthcare |
Freelance Medical Annotation involves providing detailed annotations on medical data, often for AI training, requiring medical knowledge and precision. Medical Data Labeler typically performs similar tasks but may work within a team or in a more structured environment. Both roles are essential in healthcare AI development but differ mainly in work setup and scope.

Full-time
Posted 15 days ago
Job description
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 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 (ie. PhD, PharmD, or MD) is required. CMPP preferred.
Professional Skills and Requirements:
- Candidates must have 5 or more years of relevant job experience with medical publications, including manuscripts, posters, abstracts, podium presentations, scientific platforms, and publication extenders.
- 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.
- Experience with established professional medical editorial processes (ie. AMA style) and ethical guideline working knowledge (ie. ICMJE, GPP2022) is also required.
- Experience with respiratory medicine (pulmonary) is a plus.