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Remote Clinical Data Abstractor Jobs in Raleigh, NC

COMPASS Pathways

HEOR Science Liaison

Raleigh, NC · On-site +1

$63K - $85K/yr

Location: Remote in the United States. Reports to: Director, HEOR. Roles and responsibilities ... Deliver fair-balanced, scientifically rigorous presentations on clinical data, real-world evidence ...

The Select Group

LIMS Admin

Durham, NC · On-site +1

LIMS ADMINISTRATOR | REMOTE (EST) The Select Group is seeking a talented LIMS Administrator to join ... clinical data environments TSG is an equal opportunity employer. All qualified applicants will ...

Javara Inc.

Be Seen First

Director of Business Development- Clinical Research (Remote)

Raleigh, NC · Remote

The Director of Business Development is a fully remote role. Javara is an integrated research ... Effectively manage and maintain client relationships and tracking of key events, data and action ...

New

Javara Inc.

Be Seen First

Director of Business Development- Clinical Research (Remote)

Raleigh, NC · Remote

The Director of Business Development is a fully remote role. Javara is an integrated research ... Effectively manage and maintain client relationships and tracking of key events, data and action ...

New

Icon plc

Senior Clinical Research Associate

Cary, NC · Remote

Collaborating with cross-functional teams to ensure timely and accurate data collection and ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

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Remote Clinical Data Abstractor information

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$13

$24

$38

How much do remote clinical data abstractor jobs pay per hour?

As of Jul 10, 2026, the average hourly pay for remote clinical data abstractor in Raleigh, NC is $24.62, according to ZipRecruiter salary data. Most workers in this role earn between $17.98 and $31.06 per hour, depending on experience, location, and employer.

What's the highest paid remote job?

Remote clinical data abstractors typically earn between $50,000 and $80,000 annually, depending on experience and certifications. Higher-paying remote roles in healthcare and data analysis, such as remote medical directors or senior data scientists, can exceed $100,000 per year. Specialized skills and industry demand influence compensation levels for remote jobs in this field.

What does a clinical data abstractor do?

A clinical data abstractor reviews and extracts relevant information from medical records and clinical documents to ensure accurate data collection for research, quality improvement, or regulatory purposes. They typically use electronic health record systems and must understand medical terminology and data privacy regulations. Attention to detail and accuracy are essential in this role.

What are the key skills and qualifications needed to thrive in the Remote Clinical Data Abstractor position, and why are they important?

To excel as a Remote Clinical Data Abstractor, you need a strong background in medical terminology, anatomy, and clinical documentation, often supported by experience in healthcare or a related degree. Familiarity with electronic health record (EHR) systems, data abstraction software, and certifications such as RHIA, RHIT, or CCS are highly valued. Attention to detail, self-motivation, and strong communication skills are essential soft skills in this remote role. These competencies ensure accurate extraction and management of clinical data, supporting compliance and quality improvement initiatives.

What are some common challenges faced by Remote Clinical Data Abstractors, and how can they be managed?

Remote Clinical Data Abstractors often encounter challenges such as managing large volumes of complex medical records, interpreting varied documentation styles, and maintaining accuracy under tight deadlines. Staying organized through effective time management and utilizing standardized abstraction guidelines can help mitigate these obstacles. Regular communication with clinical teams and ongoing training are also important for resolving ambiguities and staying updated on best practices. Adapting to a remote environment requires self-discipline, but with the right tools and support, most abstractors can excel and find satisfaction in the vital work they do.

What skills do you need to be a clinical data abstractor?

A clinical data abstractor needs strong attention to detail, excellent organizational skills, and familiarity with medical terminology and electronic health record systems. Proficiency in data entry, basic understanding of healthcare regulations, and the ability to review and interpret medical records are also important for accuracy and compliance.

How to become a clinical data abstractor online?

To become a remote clinical data abstractor, you typically need a healthcare-related degree or background, such as nursing or health information management, along with strong attention to detail and familiarity with medical terminology. Training programs or certifications in clinical research or data abstraction can enhance your qualifications, and proficiency with electronic health records (EHR) systems is often required. Many positions also require good organizational skills and the ability to work independently in a remote environment.

What is a Remote Clinical Data Abstractor job?

A Remote Clinical Data Abstractor is responsible for reviewing and analyzing medical records to extract key clinical data for research, quality improvement, or compliance purposes. They work remotely, often for healthcare organizations, insurance companies, or research institutions, ensuring accurate and timely data abstraction. This role requires a strong understanding of medical terminology, coding systems, and electronic health records (EHRs). Attention to detail and adherence to HIPAA regulations are essential.

What are popular job titles related to Remote Clinical Data Abstractor jobs in Raleigh, NC? For Remote Clinical Data Abstractor jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Remote Clinical Data Abstractor jobs in Raleigh, NC look for? The top searched job categories for Remote Clinical Data Abstractor jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Remote Clinical Data Abstractor jobs? Cities near Raleigh, NC with the most Remote Clinical Data Abstractor job openings:
Remote Clinical Data Abstractor jobs near you
Infographic showing various Remote Clinical Data Abstractor job openings in Raleigh, NC as of July 2026, with employment types broken down into 74% Full Time, 18% Part Time, and 8% Contract. Highlights an 100% Remote job distribution, with an average salary of $51,213 per year, or $24.6 per hour.
Clinical Scientist - Oncology - US - Remote

Clinical Scientist - Oncology - US - Remote

Worldwide Clinical Trials

Durham, NC • On-site, Remote

Full-time

Re-posted 24 days ago

Job description

Who we are

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

What the ClinicalScientistdoes at Worldwide

As a member of the Clinical Oncology Operations team, the Clinical Scientist leads the review and assessment of clinical data, ensuring it meets the highest standards of quality and integrity. This role translates complex data into clear insights, communicates trends to internal teams and clients, and supports the development of key regulatory deliverables such as clinical study reports. Working closely with cross-functional stakeholders, the Clinical Scientist helps drivetimelyproject delivery, contributes to data review strategies, andidentifiesopportunities to improve processes and elevate overall study execution.

What you will do

  • Partner with cross-functional Study Teams (Medical, Biostatistics, Data Management) to develop and execute data review plans, ensuringaccuratecollection and reporting of protocol-defined endpoints.

  • Perform ongoing review and interpretation of clinical data (efficacy and safety) across listings and visual analytics,identifyingtrendsand generating actionable insights.

  • Monitor and analyze safety events across studies and programs, supporting risk identification, escalation, and informed decision-making.

  • Communicate and present clinical findings, trends, and recommendations to Study Teams, Medicalleadership, and clients; contribute to strategic discussions and study modifications.

  • Support development of key deliverables, including clinical study reports (CSRs), regulatory documents (e.g., INDs, NDAs/BLAs, IBs), and data summaries for SRCs, DSMBs, and internal review meetings.

  • Collaborate on CRF design, data quality processes, and EDC query management;identifyprotocol deviations and ensure data integrity in partnership with internal teams and vendors.

  • Contribute to study execution and continuous improvement efforts, including dashboard/UAT support, study documentation, scientific writing (e.g., narratives, abstracts), and mentoring of junior staff.

What you will bring to the role

  • Strong knowledge of the clinical development process, study design principles, and product safety profiles.

  • Experience in clinical data analysis, interpretation, and translating insights into clinical relevance.

  • Proficiencywith electronic data capture (EDC) systems, data visualization tools, and Microsoft Office (Excel, PowerPoint, Word).

  • Solid understanding of GCP, ICH, and applicable regulatory requirements.

  • Excellent communication and presentation skills, with the ability to convey complex data clearly to diverse stakeholders.

  • Strong organizational, analytical, and problem-solving skills, with the ability to manage multiple priorities and meet deadlines.

  • Collaborative, adaptable team player with strong interpersonal skills and the ability to work effectively across all levels of an organization.

  • Sound judgment, high attention to detail, and the ability to work both independently and in fast-paced, evolving environments.

Your experience

  • Advanced clinical/science degree (e.g., PharmD, PhD, MSN, MPH, etc.) preferred.

  • 8+ of industry/related experience in Oncology human clinical trial research including review and interpretation of clinical data.

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative,innovative,and successful. We'reon a mission to hire thevery bestand are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.

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