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Clinical Research Data Abstractor Jobs (NOW HIRING)

GDIT

Clinical Research Data Analyst

Fort Liberty, NC · Hybrid

$57K - $60K/yr

The Research Data Analyst will coordinate activities associated with clinical trials in the area of Traumatic Brain Injury (TBI) and provides assurance of accurate documentation in compliance with ...

UAB

CLINICAL RESEARCH DATA COORDINATOR I

Tampa, FL · On-site

$17.95 - $29.20/hr

The ideal candidate will be experienced in Clinical trial research, have knowledge of applicable clinical research data collection requirements, including GCP and ICH guidelines. The O'Neal ...

Natera

OR · On-site

Interpret and manage complex clinical patient data for research, quality improvement, and regulatory reporting. PRIMARY RESPONSIBILITIES: * Data Abstraction: Accurately review, interpret, and ...

Natera

Sr Clinical Data Abstractor

Interpret and manage complex clinical patient data for research, quality improvement, and regulatory reporting. PRIMARY RESPONSIBILITIES: * Data Abstraction: Accurately review, interpret, and ...

Natera

Sr Clinical Data Abstractor

Austin, TX · On-site

Interpret and manage complex clinical patient data for research, quality improvement, and regulatory reporting. PRIMARY RESPONSIBILITIES: * Data Abstraction: Accurately review, interpret, and ...

Natera

Sr Clinical Data Abstractor

Interpret and manage complex clinical patient data for research, quality improvement, and regulatory reporting. PRIMARY RESPONSIBILITIES: * Data Abstraction: Accurately review, interpret, and ...

Natera

OR

Interpret and manage complex clinical patient data for research, quality improvement, and regulatory reporting. PRIMARY RESPONSIBILITIES: * Data Abstraction: Accurately review, interpret, and ...

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All JobsClinical Research Data Abstractor Jobs

Clinical Research Data Abstractor information

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$18

$44

$62

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

As of Jun 14, 2026, the average hourly pay for clinical research data abstractor in the United States is $44.13, according to ZipRecruiter salary data. Most workers in this role earn between $36.30 and $52.40 per hour, depending on experience, location, and employer.

What is the difference between Clinical Research Data Abstractor vs Clinical Research Coordinator?

AspectClinical Research Data AbstractorClinical Research Coordinator
Primary RoleExtracts and summarizes data from clinical trial recordsManages overall study operations and participant coordination
Required SkillsAttention to detail, data management, basic medical knowledgeRegulatory compliance, patient interaction, study oversight
Work EnvironmentData entry labs, clinical trial sites, research officesClinical sites, hospitals, research institutions
CertificationsTypically none required, but certifications like CCR can helpOften requires CCRC or similar certifications

While both roles support clinical research, the Clinical Research Data Abstractor focuses on data extraction and analysis, whereas the Clinical Research Coordinator manages study logistics and participant interactions. Understanding these differences helps in choosing the right career path or job search focus.

What is the movie clinical about?

The term 'clinical' in a movie typically refers to themes related to medicine, healthcare, or medical settings. It may depict medical professionals, hospitals, or health-related issues, often focusing on clinical procedures or ethical dilemmas in healthcare environments.

What does it mean for someone to be clinical?

In the context of a Clinical Research Data Abstractor, being clinical relates to working with medical or health-related data from clinical trials or patient records. It involves understanding medical terminology, ensuring data accuracy, and following regulatory guidelines to support research studies. Attention to detail and familiarity with healthcare environments are important skills for this role.

What do we mean by clinical?

In the context of a Clinical Research Data Abstractor role, 'clinical' refers to activities related to the study of health, diseases, and medical treatments involving patient data. It includes collecting, reviewing, and summarizing data from clinical trials or medical records to support research and regulatory submissions. Understanding clinical terminology and data management tools is essential for this job.

What does very clinical mean?

In the context of a Clinical Research Data Abstractor, 'very clinical' typically refers to data or processes that are highly focused on medical, scientific, or healthcare-related information. It indicates a detailed understanding of clinical terminology, protocols, and documentation standards used in clinical trials and research environments.

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

Clinical Research Data Abstractors often encounter challenges such as interpreting complex medical records, ensuring data accuracy, and navigating various electronic health record (EHR) systems. To manage these challenges, it's helpful to develop strong attention to detail, maintain up-to-date knowledge of medical terminology, and collaborate closely with clinical teams for clarification when needed. Additionally, frequent communication with data managers and adhering to standardized data abstraction protocols can greatly reduce errors and improve data quality.

What is a Clinical Research Data Abstractor?

A Clinical Research Data Abstractor is a professional responsible for collecting and extracting important data from medical records, clinical trials, or patient charts. They ensure that the data is accurate, complete, and entered into research databases or electronic systems. This role is vital in supporting clinical research studies by ensuring high-quality data for analysis, compliance, and reporting. Clinical Research Data Abstractors often work closely with research coordinators, physicians, and other healthcare professionals.

What are the key skills and qualifications needed to thrive as a Clinical Research Data Abstractor, and why are they important?

To thrive as a Clinical Research Data Abstractor, you need strong attention to detail, knowledge of medical terminology, and experience with data collection, often supported by a degree in health sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and possibly certifications like ACRP-CP or SoCRA-CCRP is common. Excellent organizational skills, critical thinking, and the ability to communicate clearly with research teams help set top performers apart. These skills ensure accurate, timely data abstraction that is vital for regulatory compliance and the integrity of clinical research studies.
More about Clinical Research Data Abstractor jobs
What cities are hiring for Clinical Research Data Abstractor jobs? Cities with the most Clinical Research Data Abstractor job openings:
What states have the most Clinical Research Data Abstractor jobs? States with the most job openings for Clinical Research Data Abstractor jobs include:
What job categories do people searching Clinical Research Data Abstractor jobs look for? The top searched job categories for Clinical Research Data Abstractor jobs are:
Clinical Research Data Abstractor jobs near you
Infographic showing various Clinical Research Data Abstractor job openings in the United States as of June 2026, with employment types broken down into 84% Full Time, 12% Part Time, and 4% Contract. Highlights an 92% In-person, 4% Hybrid, and 4% Remote job distribution, with an average salary of $91,797 per year, or $44.1 per hour.
Clinical Research & Data Coordinator

Clinical Research & Data Coordinator

Morehouse School of Medicine

Atlanta, GA • On-site

Full-time

Posted 21 days ago

Job description

Posting Details
Position Information
About MSM
Morehouse School of Medicine (MSM) is a place of distinction, serving as the nation's leading academic medical center for vulnerable populations. It's also a place for passionate individuals looking to join a dedicated community working today to help prepare tomorrow's leaders.
We exist to:
• Improve the health and well-being of individuals and communities;
• Increase the diversity of the health professional and scientific workforce;
• Address primary health care through programs in education, research and service;
With emphasis on people of color and the under-served urban and rural populations in Georgia, the nation and the world.
At Morehouse School of Medicine, we're leading the creation and advancement of health equity. You will find a fulfilling career at MSM!
Posting Number
NONAC3729
Job Title
Clinical Research & Data Coordinator
Position Title
Position Type
Non-Faculty
Number of vacancies
1
Salary
Commensurate with experience
Department
Cancer Health Equity Institute
Position Summary
The GRAIL Pathfinder II study team at the Morehouse School of Medicine is seeking a passionate and dedicated Community Outreach Coordinator/Navigator. The candidate will play a crucial role in bridging the gap between the study team and community clinics, churches, and other healthcare organizations. Expertise in identifying and engaging community leaders, including clinicians, church officials, and patient navigators, to facilitate and enhance the reach and impact of the study will be key.
POSITION ACCOUNTABILITIES AND ESSENTIAL FUNCTIONS:
  1. Study Participant Management: Oversee the electronic health records (EHRs) to identify & match study participants and screen and enroll study participants for available clinical trials.
  2. Clinical Data Management: Manage clinical trial data sets, ensuring accuracy, consistency, and security. Ensure that all clinical trial data are accurately entered into electronic data capture (EDC) systems and promptly, adhering to established protocols and guidelines.
  3. Study Coordination: Collaborate with researchers and physicians to implement health informatics solutions that support the enrollment of clinical trial participants.
  4. Study Compliance and Data Integrity: Maintain data standards, ontologies, and metadata frameworks in alignment with best practices and regulatory requirements. Ensure adherence to clinical trial regulatory requirements (IRB, HIPAA, GCP, etc.).
  5. Data Analysis: Assist with data visualization and communication of clinical and real-world data to various stakeholders.
  6. Collaboration: Contribute to the drafting of manuscripts, reports, and grants, as well as present findings at scientific meetings and conferences.

Reporting & Documentation:
  • Maintain detailed records of outreach activities, including meetings, interactions, and outcomes.
  • Prepare regular reports detailing outreach efforts, challenges, and opportunities for the leadership team.

KNOWLEDGE, SKILLS, & ABILITIES:
  • Comprehensive knowledge of local community dynamics, culture, and key stakeholders.
  • Strong organizational skills with the ability to multitask and manage multiple projects simultaneously.
  • Proficient communication skills, both written and verbal, with the ability to engage diverse audiences.
  • Familiarity with healthcare or academic research settings is an advantage.

CORE COMPETENCIES:
  1. Clinical Research Coordination: Understands clinical trial protocols, workflows, and regulatory compliance and coordinates multiple study components with precision and timeliness.
  2. Attention to Detail: Demonstrates accuracy in data entry, documentation, and review; identifies and resolves discrepancies in patient records and study data.
  3. Communication: Communicates clearly and effectively with internal and external stakeholders, including physicians, patients, and research staff, adapting messaging based on the audience and context (e.g., written, verbal, or electronic).
  4. Collaboration & Teamwork: Builds productive relationships across departments and with partner organizations and demonstrates a cooperative approach and willingness to support team goals.
  5. Patient-Centered Focus: Prioritizes patient safety, privacy, and access to appropriate clinical trials and demonstrates cultural sensitivity and empathy in patient interactions.
  6. Problem-Solving & Critical Thinking: Identifies operational challenges and proposes practical, evidence-based solutions; anticipates potential issues and takes proactive steps to minimize disruptions.
  7. Time Management & Adaptability: Manages shifting priorities in a dynamic research environment and remains flexible and calm under pressure, especially during rapid study activations.
  8. Ethical Conduct & Integrity: Upholds institutional and regulatory standards related to clinical research and handles confidential data responsibly and adheres to ethical principles.
  9. Technology Proficiency: Navigates clinical databases, electronic health records (EHRs), and research software efficiently and learns new digital tools and platforms as needed for trial coordination.
  10. Project Management: Demonstrates experience in coordinating and managing projects, ensuring objectives are met within set timeframes. Able to identify and allocate resources effectively and can anticipate and mitigate potential risks or delays.

Minimum Qualifications
  1. Minimum 2-3 years of experience working with clinical data, particularly in a research or healthcare setting.
  2. Familiarity with EHR data standards, data integration, and the ethical/legal considerations surrounding data usage.
  3. Excellent analytical, problem-solving, and organizational skills.
  4. Superior communication skills, both written and verbal.
  5. Ability to prioritize tasks and work independently, as well as part of a multi-disciplinary team.
  6. Prior experience in health-related community outreach and event organization is highly preferred.

Preferred Qualifications
  1. Experience in public health, communications, social work, or a related field.
  2. Intermediate or higher proficiency in MS Office Suite.
  3. Strong knowledge of the local community, culture, and key stakeholders.
  4. Excellent communication, interpersonal, and organizational skills.
  5. Ability to work independently and collaboratively in a team-oriented environment.

Closing Date
Open Until Filled
Yes
Special Instructions to Applicants
Employment in this role may be contingent upon extramural funding and successful performance and may be terminated or reduced in percentage of appointment if such funding is not secured or ceases to be available.
Quick Link
https://careers.msm.edu/postings/24105
EEO Statement Summary
Morehouse School of Medicine is an equal opportunity/equal access/affirmative action employer fully committed to achieving a diverse workforce and complies with all Federal and Georgia State laws, regulations, and executive orders regarding non-discrimination and affirmative action. Morehouse School of Medicine does not discriminate on the basis of race, age, color, religion, national origin or ancestry, sex, gender, disability, veteran status, genetic information, sexual orientation, or gender identity or expression.
Job Duties
Description of Job Duty
The GRAIL Pathfinder II study team at the Morehouse School of Medicine is seeking a passionate and dedicated Community Outreach Coordinator/Navigator. The candidate will play a crucial role in bridging the gap between the study team and community clinics, churches, and other healthcare organizations. Expertise in identifying and engaging community leaders, including clinicians, church officials, and patient navigators, to facilitate and enhance the reach and impact of the study will be key.
POSITION ACCOUNTABILITIES AND ESSENTIAL FUNCTIONS:
Community Engagement:
  • Identify and coordinate meetings between study staff and influential community (healthcare, churches, health promotion organizations, etc.) authorities and stakeholders, including but not limited to clinic administrators, physicians, church leaders.
  • Develop and nurture relationships with various community entities to bolster the study's visibility and engagement.

Event Organization:
  • Plan, organize, and execute community events to inform and enroll participants in the GRAIL Pathfinder II study.
  • Coordinate logistics, materials, and communication for successful event execution.

Communication & Collaboration:
  • Work closely with the principal investigator and associate director to formulate outreach strategies.
  • Provide regular updates and feedback, ensuring alignment with the study's objectives and guidelines.

KNOWLEDGE, SKILLS, & ABILITIES:
  • Strong understanding of clinical research processes and human subjects research and protections.
  • Understanding of clinical data, including data structures, standards, and ontologies29292929.
  • Familiarity with oncology trials and precision medicine concepts, particularly related to genomic testing and clinical trial matching.
  • Working knowledge of electronic health records (EHRs), clinical trial management systems (CTMS), and data entry protocols.
  • Awareness of ethical considerations related to the informed consent process and data privacy33. Also, familiarity with regulatory and ethical aspects of clinical research, including Good Clinical Practice (GCP) guidelines, Institutional Review Board (IRB) procedures, and Health Insurance Portability and Accountability Act (HIPAA) regulations.
  • Ability to build and maintain positive working relationships across interdisciplinary teams.
  • Ability to adapt quickly to changes in program needs, study protocols, and technology platforms.
  • Ability to manage multiple tasks and projects simultaneously, set priorities, and meet deadlines.
  • Ability to maintain confidentiality and protect sensitive patient and research data, upholding ethical standards and complying with all regulations applicable to clinical research.

CORE COMPETENCIES:
  1. Clinical Research Coordination: Understands clinical trial protocols, workflows, and regulatory compliance and coordinates multiple study components with precision and timeliness.
  2. Attention to Detail: Demonstrates accuracy in data entry, documentation, and review; identifies and resolves discrepancies in patient records and study data.
  3. Communication: Communicates clearly and effectively with internal and external stakeholders, including physicians, patients, and research staff, adapting messaging based on the audience and context (e.g., written, verbal, or electronic).
  4. Collaboration & Teamwork: Builds productive relationships across departments and with partner organizations and demonstrates a cooperative approach and willingness to support team goals.
  5. Patient-Centered Focus: Prioritizes patient safety, privacy, and access to appropriate clinical trials and demonstrates cultural sensitivity and empathy in patient interactions.
  6. Problem-Solving & Critical Thinking: Identifies operational challenges and proposes practical, evidence-based solutions; anticipates potential issues and takes proactive steps to minimize disruptions.
  7. Time Management & Adaptability: Manages shifting priorities in a dynamic research environment and remains flexible and calm under pressure, especially during rapid study activations.
  8. Ethical Conduct & Integrity: Upholds institutional and regulatory standards related to clinical research, handles confidential data responsibly, and adheres to ethical principles.
  9. Technology Proficiency: Navigates clinical databases, electronic health records (EHRs), and research software efficiently and learns new digital tools and platforms as needed for trial coordination.
  10. Project Management: Demonstrates experience in coordinating and managing projects, ensuring objectives are met within set timeframes. Able to identify and allocate resources effectively and can anticipate and mitigate potential risks or delays.

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