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Internship Remote Clinical Data Abstractor Jobs (NOW HIRING)

Moffitt

ABSTRACTOR ASSO/I/II/III

Chicago, IL · On-site +1

$113K - $144K/yr

... data integration in the full spectrum of all disease sites of cancer (Diagnosis; Clinical and ... REMOTE WORK allowed in the following states: AL,AZ,AR,GA,ID,IN,IA,KS,LA,MS,MO,MT,NC,OH,OK,SC,SD,TN ...

Latica AI

Clinical Data Scientist (Remote)

Latica is a community data network and clinical AI platform that enables to safely access de-identified real-world data and accelerate diagnostic and therapeutic innovation.Our platform enables fast ...

RedSail Technologies, LLC

Clinical Data Scientist

Irving, TX · On-site +1

$130K - $160K/yr

Clinical Data Scientist Job Summary The RedSail Technologies Network Services Business Unit has the ... Position is performed in a general office environment, home office, or approved remote workspace ...

Ascension

Clinical Data Analyst

Sand Springs, OK · Remote

$72K - $100K/yr

Remote Facility: Ascension St. John's Medical Group Department/Specialty: Total Quality Management ... for clinical and market teams. * Collaborate with cross-functional teams to validate payer data ...

Calyx

Clinical Data Manager I

$52K - $75K/yr

Ensures the accuracy and consistency of clinical databases by: * Reviewing data and identifying ... Other duties as assigned This role is remote. Candidates located in the following states: AZ, CT ...

University of Chicago

Abstractor Coder II

$29.97 - $45.59/hr

The role serves as a subject matter expert to clinical staff and supports revenue integrity through ... Understands HIPPA regulations, treats all patient information and data with complete ...

Carina Health Network

Clinical Data Engineer

$85K - $100K/yr

Clinical Data Engineer - Remote, Must Live in State of Colorado Join Carina Health Network and help us make Colorado communities healthier! Are you passionate about population health and interested ...

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

As of Jul 13, 2026, the average hourly pay for internship remote clinical data abstractor in the United States is $22.50, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.52 per hour, depending on experience, location, and employer.

What is an Internship Remote Clinical Data Abstractor?

An Internship Remote Clinical Data Abstractor is a trainee who works remotely to collect and organize clinical data from patient records and other healthcare documents. Their main responsibility is to review medical records, extract specific data points, and enter them into databases or electronic health record systems. This role is crucial for supporting research projects, quality improvement initiatives, and regulatory reporting in healthcare organizations. Interns in this position gain valuable experience in medical data management, health informatics, and compliance with privacy standards such as HIPAA.

What are the key skills and qualifications needed to thrive as an Internship Remote Clinical Data Abstractor, and why are they important?

To thrive as an Internship Remote Clinical Data Abstractor, you need a solid understanding of medical terminology, clinical documentation, and data management, often supported by coursework in health sciences or related fields. Familiarity with electronic health records (EHR) systems, data abstraction software, and HIPAA compliance is typically required. Attention to detail, strong analytical thinking, and effective written communication are crucial soft skills for this role. These abilities ensure accurate data extraction, maintain patient confidentiality, and support reliable clinical research or quality improvement efforts.

What are some typical challenges faced during a remote clinical data abstractor internship?

Interns in remote clinical data abstraction often face challenges related to learning complex medical terminology and understanding various electronic health record (EHR) systems. Adapting to remote communication with supervisors and team members can also require strong organizational and time management skills. Additionally, maintaining strict attention to detail is essential, as data accuracy directly impacts patient care and research outcomes. Interns are encouraged to proactively seek feedback and clarification to overcome these challenges and ensure high-quality work.

What is the difference between Internship Remote Clinical Data Abstractor vs Remote Clinical Data Coordinator?

AspectInternship Remote Clinical Data AbstractorRemote Clinical Data Coordinator
CredentialsTypically pursuing or recent graduate, no required certificationsOften requires relevant certifications or experience
Work EnvironmentRemote, internship setting, part-time or temporaryRemote, full-time, ongoing role
Employer & IndustryResearch institutions, clinical trials, healthcare companiesHospitals, research organizations, pharmaceutical companies
Search & Comparison IntentLearning about entry-level or internship roles in clinical dataUnderstanding full-time data management roles in healthcare

The Internship Remote Clinical Data Abstractor is an entry-level, temporary position ideal for students or recent graduates gaining experience in clinical data abstraction. In contrast, the Remote Clinical Data Coordinator is a more advanced, ongoing role responsible for managing and coordinating clinical data processes. Both roles are remote and industry-focused, but differ in experience level, responsibilities, and employment status.

What cities are hiring for Internship Remote Clinical Data Abstractor jobs? Cities with the most Internship Remote Clinical Data Abstractor job openings:
What are the most commonly searched types of Remote Clinical Data Abstractor jobs? The most popular types of Remote Clinical Data Abstractor jobs are:
What states have the most Internship Remote Clinical Data Abstractor jobs? States with the most job openings for Internship Remote Clinical Data Abstractor jobs include:
Internship Remote Clinical Data Abstractor jobs near you
Clinical Data Manager II/Senior Clinical Data Manager

Clinical Data Manager II/Senior Clinical Data Manager

Precision for Medicine

Remote

Full-time

Medical, Life, Retirement, PTO

Posted 10 days ago

Job description

*This position is 100% remote, but the preference is to have someone on the east coast*
Position Summary:
The Senior Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up to post database lock for assigned projects. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position will also oversee and/or perform database development and testing.
Essential functions of the job include but are not limited to:
  • Primary Data Management (DM) contact (Lead DM role) for assigned clinical project(s) / program(s), ensuring that there is back-up, continuity, responsiveness, and that tasks are performed in a timely manner. May support another Lead DM as a back-up and/or team member. May include DM oversight of sponsor programs.
  • Oversee project data entry process including development of data entry guidelines, training, data entry quality and resourcing
  • May perform quality control of data entry
  • Provide input, assesses and manage timelines. Ensure that clinical data management deadlines are met with quality. Assess resource needs for assigned projects, as needed.
  • Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders
  • May assist in building clinical databases
  • Conduct database build UAT and maintain quality controlled database build documentation. Oversee overall quality of the clinical database.
  • May specify requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. Oversee development of the edit check specifications and manual data review specifications
  • Responsible for creating, revising, appropriate versioning and maintaining data management documentation. Oversee completeness of data management documentation for the Trial Master File.
  • Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed.
  • Review and query clinical trial data according to the Data Management Plan
  • Perform line listing data review based on the guidance provided by the sponsor and/or Lead DM
  • Run patient and study level status and metric reporting
  • Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency
  • Coordinate SAE/AE reconciliation
  • Liaises with third-party vendors such as external data and EDC vendors in a projectmanager capacity in support of timelines and data-related deliverables
  • May assist with SAS programming and quality control of SAS programs used in the Data Management department
  • Identify and troubleshoot operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders
  • May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project
  • Participate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities
  • May attend strategy meetings, bid defense prep meetings, bid defenses, capability presentations, potential client engagement meetings
  • May review Request for Proposals (RFP), proposals, provide project estimates
  • Provide leadership for cross-functional and organization-wide initiatives, where applicable
  • Trains and ensures that all data management project team members have been sufficiently trained
  • Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues
  • May present software demonstrations/trainings, department/company training sessions, present at project meetings
  • May require some travel
  • Perform other duties as assigned

Qualifications:
Minimum Required:
  • Bachelors and/or a combination of related experience

Other Required:
  • 8+ years' experience as a Sr. Clinical Data Manager and 5 Years as a Clinical Data Manager II
  • Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
  • Able to handle a variety of clinical research tasks
  • Excellent organizational and communication skills
  • Professional use of the English language; both written and oral
  • Experience in utilizing various clinical database management systems
  • Broad knowledge of drug, device and/or biologic development and effective data management practices
  • Strong representational skills, ability to communicate effectively orally and in writing
  • Strong leadership and interpersonal skills
  • Ability to undertake occasional travel

Preferred:
  • Experience in a clinical, scientific or healthcare discipline
  • Dictionary medical coding (MedDRA and WHODrug)
  • Understanding of CDISC standards (CDASH, SDTM, ADaM, etc....)
  • Oncology and/or Orphan Drug therapeutic experience

Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.
Reasonable estimate of the current range
$91,500-$166,100 USD
Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com.
Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.

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