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Remote Clinical Data Abstractor Jobs in Lexington, MA

Cytel

Principal Clinical Data Manager

Cambridge, MA · Remote

Principal Clinical Data Manager United States (Remote) Responsibilities - Responsible for vendor oversight activities across global development programs. - Represents data management function on the ...

IQVIA

Senior Data Team Lead (Remote)

Boston, MA · Remote

$86K - $217K/yr

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

IQVIA

Senior Data Team Lead (Remote)

Boston, MA · Remote

$86K - $217K/yr

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

DRC Systems

Technical Lead - Data Analysis

Boston, MA · Remote

$50 - $54/hr

Title - Technical Lead - Data Analysis Location - Boston, MA - Remote JD - Key Skills * Advanced ... Deep expertise in claims and/or clinical data * Strong understanding of medical economics, risk ...

Whoop

Director, Clinical Operations

Boston, MA · On-site +1

Oversee Clinical Data Management and clinical trial technologies, ensuring high-quality, timely ... ePRO, eTMF, and remote study platforms. * Oversee study startup and regulatory operations ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

Lead cross-functional meetings with the Clinical Development, Clinical Operations, Data Management ... Perform clinical research site activities, which can include onsite or remote monitoring, co ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

Lead cross-functional meetings with the Clinical Development, Clinical Operations, Data Management ... Perform clinical research site activities, which can include onsite or remote monitoring, co ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

Lead cross-functional meetings with the Clinical Development, Clinical Operations, Data Management ... Perform clinical research site activities, which can include onsite or remote monitoring, co ...

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Remote Clinical Data Abstractor information

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

As of Jul 28, 2026, the average hourly pay for remote clinical data abstractor in Lexington, MA is $28.46, according to ZipRecruiter salary data. Most workers in this role earn between $20.82 and $35.91 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 cities near Lexington, MA are hiring for Remote Clinical Data Abstractor jobs? Cities near Lexington, MA 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 Lexington, MA as of July 2026, with employment types broken down into 43% Full Time, and 57% Contract. Highlights an 100% Remote job distribution, with an average salary of $59,196 per year, or $28.5 per hour.
Principal Clinical Data Manager

Principal Clinical Data Manager

Cytel

Cambridge, MA • Remote

Full-time

Posted 11 days ago

Job description

Principal Clinical Data Manager United States (Remote) JOB DESCRIPTION Responsibilities - Responsible for vendor oversight activities across global development programs. - Represents data management function on the Clinical Sub-team ensuring aligned expectations between the CRO and client for all data related deliverables, especially in support of key decision points and regulatory submissions. - Contributes influential leadership in collaboration with other client Stakeholders to ensure established milestones and deliverables are met with the highest degree of quality. - Partners with appropriate stakeholders and CRO partners to mitigate and resolve risks. - Provides input to functional governance with client strategic suppliers. Partners with appropriate stakeholders to resolve issues escalated from the vendor and/or cross-functional teams. - Participates in preparing function for submission readiness and may represent function in a formal inspection or audit. - Participates and represents function in formal inspections and audits as requested. - Ensure archival and inspection readiness of all Data Management Trial Master File (TMF) documents. Ensures achievement of major data management deliverables and milestones in coordination with other functions including the Therapeutic Area Units, Clinical Operations, Statistical Programming and Statistics. - Responsible for the planning and management of external Data Management budgets and timelines to ensure accuracy, understand trends in variances and support continuous improvement in forecasting. - Acts as a process expert for operational and oversight models. - Maintains SOPs, process maps and templates and timelines to support functions operational and oversight models. - May prepare metrics to support the function’s KPIs. - Represents function in external professional initiatives and organizations such as SCDM, CDISC, DIA, etc. to identify industry best practice and increase the visibility of client. - Contributes or Leads functional Continuous Improvement initiatives, providing strategic direction and identifying key deliverables that meet timelines, budget, and are in alignment with company, departmental or functional requirements. - Ensure compliance with own Learning Curricula, corporate and/or GXP requirements. - Works cross-functionally to ensure the quality of the data in each database and on time delivery, as well as quality of other data management deliverables. - Performs other duties as assigned Qualifications Educational qualifications: - MS or BS in health-related, life sciences area or technology-related field. Minimum Work Requirements: - Minimum of 10 years data management and/or drug development process with expertise in the cross-functional interfaces with the data management function. - Proven track record of strong project management skills and experience managing data management activities for large drug development programs. - Experience with all phases of development in one or more therapeutic areas preferred. - Ability to handle multiple development programs simultaneously. - NDA/CTD Experience preferred. - Strong knowledge of data management best practices & technologies as applied to clinical trials. - Solid understanding of clinical trial documents (protocols, statistical analysis plans, CRFs, study reports) and processes. - Expert knowledge of FDA and ICH regulations and industry standards applicable to data capture and data management process. - Advanced knowledge of broad drug development process with expertise in the cross-functional interfaces with the data management function. APPLY NOW JOB INFO Job Identification 1311 Job Category Clinical Data Insights & Analytics Posting Date 17/02/2026, 00:38 Locations Remote, Cambridge, MA, 02139, US (Remote)

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