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Clinical Research Coder Jobs (NOW HIRING)

Wake Research

Clinical Research Coordinator

Chattanooga, TN · On-site

$22 - $29.25/hr

The Clinical Research Coordinator (CRC) is a specialized research professional working with and ... Familiarity with the Code of Federal Regulations as they pertain to human subject protection

Adams Clinical

Clinical Research Coordinator II

Desoto, TX · On-site

$55K - $64K/yr

Philadelphia, PA; and Dallas, TX. We are seeking experienced applicants for the Clinical Research Coordinator II role at our Dallas location (Zip Code: 75115). This role is ideal for coordinators ...

Adams Clinical

Clinical Research Coordinator II

Desoto, TX · On-site

$55K - $64K/yr

Philadelphia, PA; and Dallas, TX. We are seeking experienced applicants for the Clinical Research Coordinator II role at our Dallas location (Zip Code: 75115). This role is ideal for coordinators ...

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How much do clinical research coder jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for clinical research coder in the United States is $30.16, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $31.97 per hour, depending on experience, location, and employer.

What does a Clinical Research Coder do?

A Clinical Research Coder is responsible for reviewing clinical research documentation and assigning standardized medical codes to diagnoses, procedures, and treatments. This role ensures that data collected during clinical trials is accurately coded for analysis, reporting, and regulatory compliance. Clinical Research Coders work closely with clinical research teams to maintain data integrity, support billing processes, and facilitate research outcomes. They must be familiar with medical terminology, coding systems such as ICD and CPT, and regulatory requirements related to clinical trials.

How does a Clinical Research Coder typically interact with clinical research teams and principal investigators?

Clinical Research Coders work closely with clinical research teams, including principal investigators, study coordinators, and data managers, to ensure that medical procedures and diagnoses are accurately translated into standardized codes. These professionals often participate in regular meetings to clarify clinical documentation, resolve coding discrepancies, and ensure adherence to regulatory and billing requirements. Their collaborative efforts help maintain data integrity and compliance, supporting the smooth operation of research studies and the accurate reporting of outcomes.

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

To thrive as a Clinical Research Coder, you need a strong understanding of medical terminology, coding systems (like ICD-10 and CPT), and clinical research protocols, often supported by a degree in health information management or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certification such as Certified Professional Coder (CPC) are commonly required. Attention to detail, analytical thinking, and effective communication skills help ensure accurate data coding and collaboration with research teams. These skills and qualifications are essential for maintaining data integrity, regulatory compliance, and efficient clinical research operations.

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

AspectClinical Research CoderClinical Data Coordinator
CredentialsCertification in medical coding, clinical research experienceOften requires clinical data management training, sometimes certifications
Work EnvironmentResearch sites, hospitals, clinical trial settingsData management departments, research organizations
Employer & IndustryPharmaceutical companies, research institutionsHospitals, research organizations, CROs
Primary FocusAccurate coding of clinical trial dataManaging and ensuring data quality and integrity

While both roles support clinical research, Clinical Research Coders focus on coding and classifying clinical trial data, whereas Clinical Data Coordinators manage overall data collection and quality assurance. Both positions require knowledge of clinical terminology and data management, but their daily tasks and responsibilities differ.

What cities are hiring for Clinical Research Coder jobs? Cities with the most Clinical Research Coder job openings:
What states have the most Clinical Research Coder jobs? States with the most job openings for Clinical Research Coder jobs include:
Clinical Research Coder jobs near you
Clinical Research Coordinator

Clinical Research Coordinator

Wake Research

Irvine, CA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago

Job description

Company Description

M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the largest independent, multi-site clinical research companies in the US. M3 Wake Research continues to grow through acquisitions and uncompromising commitment to careful planning and execution in accordance with regulatory compliance.

Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential clinical trial participants across the US. As of today, our board-certified physicians have completed more than 7,000+ successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data.

Due to our continued growth, we are hiring for a Clinical Research Coordinator at Wake Research, an M3 company. This position is on-site and located in Irvine, CA.  

Job Description

The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI).  While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC manages, supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. 

Essential Duties and Responsibilities:

  • Assisting trial Investigator in screening and review of potential study participants eligibility
  • Maintaining case report forms, charts and documentation
  • Mentoring, training, and high-level oversight of other clinical research coordinators and research assistants
  • Ensuring that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements
  • Collecting and entering data as necessary
  • Assist management with potential new hire selection and shadowing process
  • Assist with study start-up, maintenance, and close-out of studies as needed for those on the team
  • Ability to be flexible with study assignments
Qualifications
  • Clinical Research Coordinator with 2+ years of experience
  • Phlebotomy & EKG experience strongly preferred
  • Excellent verbal & written communication skills
  • Ability to learn quickly, read and understand complex protocols, follow very detailed directions, and multi-tasking
  • Must be able to maintain strict confidentiality of patients, employees, and company information at all times and adhere to HIPAA Guidelines
  • Extensive clinical trial knowledge through education and/or experience
  • Successful completion of GCP Certification and Advanced CRC preferred
  • Detail-oriented
  • Familiarity with the Code of Federal Regulations as they pertain to human subject protection
  • Strong interpersonal skills

Additional Information

About M3: 

M3 USA is at the forefront of healthcare innovation, offering digital solutions across healthcare, life sciences, pharmaceuticals, and more. Since our inception in 2000, we’ve seen remarkable growth, fueled by our mission to utilize the internet for a healthier world and more efficient healthcare systems.

Our success is anchored in our trusted digital platforms that engage physician communities globally, facilitating impactful medical education, precise job placement, and insightful market research. M3 USA prides itself on a dynamic and innovative work environment where every team member contributes to global health advancements.

Joining M3 USA means being part of a dedicated team striving to make a significant difference in healthcare. We provide a unique opportunity for you to be at the cutting edge of healthcare innovation, shaping the future in a meaningful career. Embrace the chance to drive change with M3 USA.

Benefits: 

A career opportunity with M3 Wake Research offers competitive wages, and benefits such as:

  • 401(k), 401(k) matching
  • Dental insurance
  • Disability insurance
  • Employee assistance program
  • Flexible spending account
  • Health insurance
  • Life insurance
  • Paid time off
  • Vision insurance

*This position offers a competitive pay rate of $30–$40 per hour.

*M3 reserves the right to change this job description to meet the business needs of the organization

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