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Full Time Clinical Data Coding Jobs (NOW HIRING)

Belcan

Clinical Data manager

Durham, NC · On-site

$55 - $65/hr

Zip Code: 27701 Area Code: 919, 984 Start Date: Right Away Contract: 9 months Keywords: #DurhamJobs; #ClinicalDatamanagerJobs ; Job Summary: The Clinical Data Manager will apply his or her knowledge ...

Belcan

Clinical Data manager

Durham, NC · On-site

$55 - $65/hr

Zip Code: 27701 Area Code: 919, 984 Start Date: Right Away Contract: 9 months Keywords: #DurhamJobs; #ClinicalDatamanagerJobs; Job Summary: The Clinical Data Manager will apply his or her knowledge ...

TalentBurst, Inc.

Clinical Data manager

Durham, NC · On-site

Title: Clinical Data manager Location: Durham, NC 27709 Duration: 9 Months Job Summary: The ... Develops project-specific eCCG, data management plans that address areas such as data coding ...

University of Utah

Clinical Data Managers

Campus, IL · On-site +1

$50.91K - $69.59K/yr

... Code? No Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule ... Build, review, and maintain clinical databases, data collection tools, and applications. Create ...

University of Utah

Clinical Data Managers

Campus, IL · On-site +1

$50.91K - $69.59K/yr

... Code? No Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule ... Build, review, and maintain clinical databases, data collection tools, and applications. Create ...

University of Utah

Clinical Data Managers

Campus, IL · On-site +1

$50.91K - $69.59K/yr

... Code? No Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule ... Build, review, and maintain clinical databases, data collection tools, and applications. Create ...

University of Utah

Clinical Data Managers

Salt Lake City, UT · On-site +1

$50.91K - $69.59K/yr

... Code? No Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule ... Build, review, and maintain clinical databases, data collection tools, and applications. Create ...

University of Utah

Clinical Data Managers

Salt Lake City, UT · On-site

$34.77K - $84.20K/yr

... Code? No Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule ... Build, review, and maintain clinical databases, data collection tools, and applications. Create ...

ImmunityBio, Inc.

Clinical Data Manager

Position Summary The Clinical Data Manager is an expert in clinical data management with ... Coding Guidelines * Annotated CRFs * Edit Check Specifications * Attend study-specific team ...

Centria Autism

Clinical Data Analyst

Farmington Hills, MI · On-site

$105K - $115K/yr

The Clinical Data Analyst partners with clinical leadership, payor relations, and operations to ... Compliance with Centria's Code of Conduct, policies and procedures, and Federal and State laws.

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Full Time Clinical Data Coding information

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How much do full time clinical data coding jobs pay per hour?

As of Jun 3, 2026, the average hourly pay for full time clinical data coding in the United States is $57.17, according to ZipRecruiter salary data. Most workers in this role earn between $45.19 and $68.03 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Full Time Clinical Data Coder, and why are they important?

To thrive as a Full Time Clinical Data Coder, you need a strong understanding of medical terminology, anatomy, and disease classification systems, typically supported by certification such as CPC, CCS, or CCA. Proficiency in coding software (e.g., 3M, EPIC), ICD-10, CPT, and electronic health records (EHR) systems is essential. Attention to detail, analytical thinking, and effective communication are crucial soft skills for ensuring accuracy and collaborating with healthcare professionals. These skills are important because they ensure precise coding, regulatory compliance, and optimized reimbursement for healthcare organizations.

What are some typical challenges faced by professionals in Full Time Clinical Data Coding roles, and how can they be managed?

Professionals in Full Time Clinical Data Coding often encounter challenges such as staying updated with frequent changes in medical coding standards (like ICD-10, CPT), ensuring high accuracy under tight deadlines, and managing large volumes of complex clinical data. To manage these challenges, it’s important to participate in ongoing training, utilize coding software and resources efficiently, and collaborate closely with clinical and administrative teams to clarify ambiguous documentation. Effective time management and attention to detail are key to maintaining compliance and data integrity in this fast-paced environment.

What is a Full Time Clinical Data Coding job?

A Full Time Clinical Data Coding job involves reviewing clinical documentation and assigning standardized codes to diagnoses, procedures, and other medical information. These codes are essential for billing, insurance claims, compliance, and data analysis in healthcare settings. Professionals in this role ensure that all patient records are accurately coded according to established medical classification systems, such as ICD-10 or CPT. This helps maintain data integrity, supports research, and facilitates smooth operations within healthcare organizations.

What is the difference between Full Time Clinical Data Coding vs Medical Records Technician?

AspectFull Time Clinical Data CodingMedical Records Technician
CertificationsAHIMA or AAPC coding certificationsRHIT or RHIA certifications often preferred
Work EnvironmentHospitals, clinics, healthcare organizationsMedical facilities, health information departments
Job FocusAssigning codes to diagnoses and procedures for billing and recordsOrganizing, maintaining, and retrieving patient records

Full Time Clinical Data Coding involves assigning standardized codes to medical diagnoses and procedures, primarily for billing and data analysis, often requiring coding certifications. Medical Records Technicians focus on organizing and managing patient records, ensuring accuracy and confidentiality. While both roles work within healthcare settings, Clinical Data Coders are more involved in coding and billing processes, whereas Medical Records Technicians handle record management and retrieval tasks.

What cities are hiring for Full Time Clinical Data Coding jobs? Cities with the most Full Time Clinical Data Coding job openings:
What are the most commonly searched types of Clinical Data Coding jobs? The most popular types of Clinical Data Coding jobs are:
Full Time Clinical Data Coding jobs near you
Clinical Data Manager/Clinical Data Reviewer

Clinical Data Manager/Clinical Data Reviewer

Charles River Laboratories

Manhattan, NY • Remote

Full-time

Medical, Vision, Retirement

Posted 13 days ago

Charles River Laboratories rating

8.2

Company rating: 8.2 out of 10

Based on 90 frontline employees who took The Breakroom Quiz

26th of 71 rated pharmaceutical

Job description

Clinical Data Manager/Clinical Data Reviewer Join to apply for the Clinical Data Manager/Clinical Data Reviewer role at Charles River Laboratories For 75+ years, Charles River has advanced the discovery, development, and safe manufacture of new drug therapies. Join a global team where your expertise directly supports healthier lives worldwide. We are seeking an experienced Clinical Data Manager/Clinical Data Reviewer to join our Safety Assessment business on a full-time, permanent, remote basis (UK or EU).

In this role, you'll support end-to-end clinical data management processes, ensure data integrity, and collaborate closely with clients across multiple complex studies. Clinical Data Management & Transfer Prepare and review Data Transfer Agreements for all assay data types. Build strong client relationships through regular meetings and data presentations.

Create and QC SDTM and non-SDTM datasets . Ensure all datasets meet regulatory standards and are delivered securely. Use approved data exchange platforms for compliant data transfers.

Data Review & Quality Review clinical trial data for accuracy, completeness, and protocol adherence. Validate data coding, interpretation, and consistency. Conduct robust QC checks across all study documentation and regulatory requirements.

Partner with internal teams and external clients throughout the data lifecycle. Mentor and support peers; serve as team lead when applicable (Manager level). Host and participate in internal/external meetings to maintain project alignment.

Process Improvement Develop and maintain templates, tools, and SOPs. Lead or support initiatives focused on data automation and workflow enhancement (Manager level). What You Bring Education Bachelor's degree in a scientific discipline (preferred).

Experience Strong background in a research or pharmaceutical environment with hands‐on clinical data management and clinical data review experience. CRO/Pharma industry experience preferred. Comfortable in customer‐facing roles; able to build and maintain strong stakeholder relationships.

Technical Skills Knowledge of CDISC standards (CDASH, SDTM, Controlled Terminology). Experience with common data formats (.xml, .xpt, sas7bdat, ASCII, .DAT, .xlsx). Proficiency in Microsoft Office; able to learn validated systems quickly.

Soft Skills Excellent communication, organizational, and leadership abilities. Ability to manage complex workloads under tight timelines. At Manager level: exceptional customer service and relationship‐building skills.

If you're passionate about data integrity, collaboration, and advancing global health, we'd love to hear from you. Apply today and make an impact with Charles River. Seniority level Mid‐Senior level Employment type Full-time Job function Science Benefits Medical insurance Vision insurance 401(k) Pension plan Paid paternity leave #J-18808-Ljbffr

What Charles River Laboratories employees say

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About Charles River

Sourced by ZipRecruiter

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947

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