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Freelance Clinical Data Coding Jobs (NOW HIRING)

Belcan

Clinical Data Manager

Durham, NC

$55 - $65/hr

Clinical Data Manager Location: Durham, NC Duration: 09 Months contract (Potential temp to Perm ... Develops project-specific eCCG, data management plans that address areas such as data coding ...

Belcan

Clinical Data Manager

Durham, NC

$55 - $65/hr

Clinical Data Manager Location: Durham, NC Duration: 09 Months contract(Potential temp to Perm ... Develops project-specific eCCG, data management plans that address areas such as data coding ...

Intellectt Inc

Clinical Data Manager

Durham, NC

Develops project-specific eCCG, data management plans that address areas such as data coding ... Processes clinical data transfers including receipt, entry, verification, or filing of information.

Intellectt INC

Clinical Data Manager

Durham, NC · On-site

Develops project-specific eCCG, data management plans that address areas such as data coding ... Processes clinical data transfers including receipt, entry, verification, or filing of information.

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 ...

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 ...

Medpace, Inc.

Clinical Data Coder

Cincinnati, OH · On-site

$18 - $22.75/hr

... based Clinical Data Coder to join our Clinical Coding & Support team in Cincinnati, OH. This ... Perform accurate coding of medical terms and medications utilizing industry-wide standards as well ...

Medpace, Inc.

Clinical Data Coder

Cincinnati, OH · On-site

$18 - $22.75/hr

... based Clinical Data Coder to join our Clinical Coding & Support team in Cincinnati, OH. This ... Perform accurate coding of medical terms and medications utilizing industry-wide standards as well ...

University of Utah

Clinical Data Managers

Campus, IL · On-site +1

$50.91K - $69.59K/yr

Job Code: P57161 Grade: P12 Expected Pay Range: $34,771 to $52,705 Clinical Data Manager, II Requires moderate skill set and proficiency in discipline. Conducts work assignments of increasing ...

University of Utah

Clinical Data Managers

Campus, IL · On-site +1

$50.91K - $69.59K/yr

Job Code: P57161 Grade: P12 Expected Pay Range: $34,771 to $52,705 Clinical Data Manager, II Requires moderate skill set and proficiency in discipline. Conducts work assignments of increasing ...

University of Utah

Clinical Data Managers

Campus, IL · On-site +1

$50.91K - $69.59K/yr

Job Code: P57161 Grade: P12 Expected Pay Range: $34,771 to $52,705 Clinical Data Manager, II Requires moderate skill set and proficiency in discipline. Conducts work assignments of increasing ...

ImmunityBio

Clinical Data Manager

Culver City, CA · On-site +1

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 ...

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Freelance Clinical Data Coding information

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How much do freelance clinical data coding jobs pay per year?

As of Jun 4, 2026, the average yearly pay for freelance clinical data coding in the United States is $70,839.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,000.00 and $81,000.00 per year, depending on experience, location, and employer.

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

To thrive as a Freelance Clinical Data Coder, you need a strong understanding of medical terminology, clinical documentation, and coding standards (such as ICD-10 and CPT), often supported by certification like CCS or CPC. Familiarity with coding software, electronic health records (EHR) systems, and data management tools is typically required. Strong attention to detail, self-motivation, and effective communication skills help ensure accuracy and client satisfaction in remote settings. These skills are critical to producing compliant, error-free coding that supports proper billing, reporting, and healthcare decision-making.

What are some common challenges freelancers face when working in clinical data coding, and how can they be addressed?

Freelance clinical data coders often encounter challenges such as staying updated with evolving medical coding standards and ensuring data accuracy across multiple client systems. Additionally, they may face difficulties in accessing sufficient training or support, and managing varying workflows from different organizations. To address these issues, freelancers can invest in continuous education, join professional associations, and utilize coding resources and forums to stay current. Building strong communication channels with clients also helps clarify project expectations and maintain high-quality deliverables.

What is freelance clinical data coding?

Freelance clinical data coding involves independently assigning standardized codes to medical diagnoses, procedures, and clinical information collected during clinical trials or research studies. Clinical data coders use coding systems such as MedDRA or WHO Drug Dictionary to ensure data consistency and regulatory compliance. As freelancers, they typically work remotely for pharmaceutical companies, contract research organizations, or healthcare institutions, providing flexible support for clinical research projects. Their work is essential for accurate data analysis, reporting, and regulatory submissions.

What is the difference between Freelance Clinical Data Coding vs Freelance Medical Coding?

AspectFreelance Clinical Data CodingFreelance Medical Coding
CredentialsCertifications like CCS, CPC, or CCA; knowledge of clinical trialsCertifications like CPC, CCS, or CCA; focus on medical billing and coding
Work EnvironmentRemote, project-based, often with research organizations or pharma companiesRemote, healthcare providers, insurance companies, or billing services
Industry UsagePrimarily in clinical research, pharmaceutical, and biotech sectorsHealthcare, hospitals, clinics, insurance, and billing companies

Freelance Clinical Data Coding involves coding clinical trial data for research purposes, requiring clinical knowledge and specific certifications. Freelance Medical Coding focuses on assigning codes to medical diagnoses and procedures for billing, with a broader healthcare industry application. Both roles are remote and require certification, but they serve different industry needs and environments.

What cities are hiring for Freelance Clinical Data Coding jobs? Cities with the most Freelance 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:
What states have the most Freelance Clinical Data Coding jobs? States with the most job openings for Freelance Clinical Data Coding jobs include:
Freelance 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

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

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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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