Clinical Data Coder - Oncology (1099 only, NO C2C)
Marlborough, MA · On-site
$19.50 - $24.75/hr
Monitor coding metrics and quality indicators, proactively identifying trends and areas for improvement.
Quick apply
Marlborough, MA · On-site
$19.50 - $24.75/hr
Monitor coding metrics and quality indicators, proactively identifying trends and areas for improvement.
Quick apply
Marlborough, MA · On-site
$19.50 - $24.75/hr
Monitor coding metrics and quality indicators, proactively identifying trends and areas for improvement.
Cambridge, MA · On-site +1
$197K - $266K/yr
... data coding, cleaning, database lock and archiving; * Supervise the execution of cross-functional, internal data review plans by direct reports across all Alnylam clinical studies; * Partner with ...
Cambridge, MA · On-site +1
$197K - $266K/yr
... data coding, cleaning, database lock and archiving; * Supervise the execution of cross-functional, internal data review plans by direct reports across all Alnylam clinical studies; * Partner with ...
Cambridge, MA · On-site
$197K - $266K/yr
... data coding, cleaning, database lock and archiving; * Supervise the execution of cross-functional, internal data review plans by direct reports across all Alnylam clinical studies; * Partner with ...
Cambridge, MA · On-site
$197K - $266K/yr
... data coding, cleaning, database lock and archiving; * Supervise the execution of cross-functional, internal data review plans by direct reports across all Alnylam clinical studies; * Partner with ...
Support medical coding activities using MedDRA and WHODrug, as applicable. * Contribute to clinical data review meetings and help prepare data outputs for internal decision-making. * Maintain data ...
Support medical coding activities using MedDRA and WHODrug, as applicable. * Contribute to clinical data review meetings and help prepare data outputs for internal decision-making. * Maintain data ...
$115K - $145K/yr
Support medical coding activities using MedDRA and WHODrug, as applicable. * Contribute to clinical data review meetings and help prepare data outputs for internal decision-making. * Maintain data ...
$115K - $145K/yr
Support medical coding activities using MedDRA and WHODrug, as applicable. * Contribute to clinical data review meetings and help prepare data outputs for internal decision-making. * Maintain data ...
Burlington, MA · Hybrid
Produce medical monitor, coding listings and ad hoc listings for team review (Jreview, SAS ... Minimum of 5 years of experience in clinical data management within the pharmaceutical or ...
Burlington, MA · Hybrid
Produce medical monitor, coding listings and ad hoc listings for team review (Jreview, SAS ... Minimum of 5 years of experience in clinical data management within the pharmaceutical or ...
Boston, MA · On-site
$115K - $145K/yr
Support medical coding activities using MedDRA and WHODrug, as applicable. * Contribute to clinical data review meetings and help prepare data outputs for internal decision-making. * Maintain data ...
Boston, MA · On-site
$115K - $145K/yr
Support medical coding activities using MedDRA and WHODrug, as applicable. * Contribute to clinical data review meetings and help prepare data outputs for internal decision-making. * Maintain data ...
Burlington, MA · On-site
$145K - $160K/yr
Produce medical monitor, coding listings and ad hoc listings for team review (Jreview, SAS ... Minimum of 5 years of experience in clinical data management within the pharmaceutical or ...
Burlington, MA · On-site
$145K - $160K/yr
Produce medical monitor, coding listings and ad hoc listings for team review (Jreview, SAS ... Minimum of 5 years of experience in clinical data management within the pharmaceutical or ...
Cambridge, MA · On-site
Managing the collection, validation, coding and storage of clinical program data; enforcing standardization to maximize global data integration and inter-program efficiency. Directing the work of ...
Cambridge, MA · On-site
Managing the collection, validation, coding and storage of clinical program data; enforcing standardization to maximize global data integration and inter-program efficiency. Directing the work of ...
Oversee medical coding (MedDRA, WHODrug) and risk-based data quality review through listings ... Minimum of 7 years of clinical data management experience in industry-sponsored clinical trials ...
Quick apply
Oversee medical coding (MedDRA, WHODrug) and risk-based data quality review through listings ... Minimum of 7 years of clinical data management experience in industry-sponsored clinical trials ...
Position Summary The Clinical Data Coordinator is responsible for clinical data entry activities ... GCPs, ICH, and Code of Federal Regulations. * Clinical study experience in the field of Oncology.
Position Summary The Clinical Data Coordinator is responsible for clinical data entry activities ... GCPs, ICH, and Code of Federal Regulations. * Clinical study experience in the field of Oncology.
$130K - $150K/yr
Support SAE reconciliation and medical coding activities * Develop data transfer agreements with third parties * Generate ad hoc data listings to support medical, clinical operations and ...
$130K - $150K/yr
Support SAE reconciliation and medical coding activities * Develop data transfer agreements with third parties * Generate ad hoc data listings to support medical, clinical operations and ...
Waltham, MA · On-site
$130K - $150K/yr
Support SAE reconciliation and medical coding activities * Develop data transfer agreements with third parties * Generate ad hoc data listings to support medical, clinical operations and ...
Waltham, MA · On-site
$130K - $150K/yr
Support SAE reconciliation and medical coding activities * Develop data transfer agreements with third parties * Generate ad hoc data listings to support medical, clinical operations and ...
Waltham, MA · On-site
$130K - $150K/yr
Support SAE reconciliation and medical coding activities * Develop data transfer agreements with third parties * Generate ad hoc data listings to support medical, clinical operations and ...
Quick apply
Waltham, MA · On-site
$130K - $150K/yr
Support SAE reconciliation and medical coding activities * Develop data transfer agreements with third parties * Generate ad hoc data listings to support medical, clinical operations and ...
Oversee medical coding (MedDRA, WHODrug) and risk-based data quality review through listings ... Minimum of 7 years of clinical data management experience in industry-sponsored clinical trials ...
Oversee medical coding (MedDRA, WHODrug) and risk-based data quality review through listings ... Minimum of 7 years of clinical data management experience in industry-sponsored clinical trials ...
Strong knowledge of EDC systems, clinical data standards, medical coding, and data reconciliation processes * Experience supporting major regulatory submissions, such as NDA, BLA, or MAA * Proven ...
Strong knowledge of EDC systems, clinical data standards, medical coding, and data reconciliation processes * Experience supporting major regulatory submissions, such as NDA, BLA, or MAA * Proven ...
Lead all clinical data management activities across multiple programs from IND through BLA ... Oversee CRF design, database build, edit checks, data review, coding, reconciliation, and database ...
Lead all clinical data management activities across multiple programs from IND through BLA ... Oversee CRF design, database build, edit checks, data review, coding, reconciliation, and database ...
Cambridge, MA · On-site
$245K - $276K/yr
Strong knowledge of EDC systems, clinical data standards, medical coding, and data reconciliation processes * Experience supporting major regulatory submissions, such as NDA, BLA, or MAA * Proven ...
Cambridge, MA · On-site
$245K - $276K/yr
Strong knowledge of EDC systems, clinical data standards, medical coding, and data reconciliation processes * Experience supporting major regulatory submissions, such as NDA, BLA, or MAA * Proven ...
Cambridge, MA · Remote
$130K - $209K/yr
... coding guidelines, Serious Adverse Events (SAE) reconciliation guidelines, and database lock plans. * Lead data review, including query management, and activities required for interim and final ...
Cambridge, MA · Remote
$130K - $209K/yr
... coding guidelines, Serious Adverse Events (SAE) reconciliation guidelines, and database lock plans. * Lead data review, including query management, and activities required for interim and final ...
Lead all clinical data management activities across multiple programs from IND through BLA ... Oversee CRF design, database build, edit checks, data review, coding, reconciliation, and database ...
Lead all clinical data management activities across multiple programs from IND through BLA ... Oversee CRF design, database build, edit checks, data review, coding, reconciliation, and database ...
$21.79 - $27.95
4% of jobs
$27.95 - $34.11
10% of jobs
$34.11 - $40.26
2% of jobs
$40.26 - $46.42
4% of jobs
$49.50 is the 25th percentile. Wages below this are outliers.
$46.42 - $52.58
9% of jobs
$52.58 - $58.74
10% of jobs
The median wage is $63.87 / hr.
$58.74 - $64.89
13% of jobs
$64.89 - $71.05
17% of jobs
$72.86 is the 75th percentile. Wages above this are outliers.
$71.05 - $77.21
18% of jobs
$77.21 - $83.37
7% of jobs
$83.37 - $89.52
5% of jobs
$21
$62
$89
A Clinical Data Coding job involves assigning standardized medical codes to clinical data, such as diagnoses, procedures, and treatments, to ensure accurate documentation and facilitate healthcare analytics, billing, and research. Professionals in this role use coding systems like ICD, CPT, and SNOMED CT to classify medical information. They work with electronic health records (EHRs) and collaborate with healthcare providers, data analysts, and regulatory bodies. Accuracy and attention to detail are crucial, as coded data impacts patient care, compliance, and reimbursement.
To thrive in Clinical Data Coding, strong knowledge of medical terminology, clinical research processes, and disease classification systems (such as ICD-10 or MedDRA) is generally required, often supported by a degree in life sciences or related fields. Familiarity with electronic data capture systems, clinical trial databases, and specialized coding software is essential, along with certifications like Certified Clinical Data Manager (CCDM) or Certified Clinical Research Professional (CCRP) being advantageous. Attention to detail, analytical thinking, and effective communication enhance quality and teamwork in this role. These skills and qualities ensure precise and compliant data coding, which is critical for research integrity, regulatory submissions, and high-quality clinical outcomes.
A typical day in Clinical Data Coding involves reviewing clinical trial data, assigning accurate codes to medical terms, adverse events, and procedures using standard classification systems, and ensuring compliance with regulatory standards. You’ll collaborate closely with clinical data managers, medical reviewers, and biostatisticians to resolve discrepancies and maintain data integrity. Additionally, you may attend team meetings to discuss coding conventions or project updates and perform quality checks on coded data. This role offers a structured environment where attention to detail and accuracy are highly valued, supporting the success of clinical research projects.

$19.50 - $24.75/hr
Contractor
Posted 14 days ago
We are an Information Technology and Business Consulting firm specializing in Project-based Solutions and Professional Staffing Services. Please have a look at below position which is with our Client and let me know your interest ASAP. I would really appreciate if you could send me your MOST RECENT UPDATED RESUME:
Need strong Clinical Data Coder with Oncology, Clinical Trials, ICH, Good Clinical Practice, FDA regulations, Rave Coder, MedDRA, WHO Drug dictionaries Exp.
Consultant LinkedIn profile must have been created before 2018/2019
Need 8-10+yrs of IT Exp. Profiles
Job Overview
We are seeking a detail-oriented and technically proficient Clinical Data Coder to support the accurate and timely coding of medical and medication terms within our electronic data capture (EDC) systems, primarily Rave Coder. This role is critical to ensuring data integrity and regulatory compliance across oncology clinical trials.
Skills: Job Duties and Responsibilities
Perform ongoing medical and medication coding using Rave Coder in accordance with MedDRA and WHO Drug dictionaries.
Review and resolve auto-coded and manually coded terms, ensuring alignment with SMPA coding conventions and internal SOPs
Collaborate with Clinical Data Managers to clarify ambiguous or unclear verbatim terms and issue coding queries when necessary
Maintain coding listings and ensure all terms are coded and approved prior to database lock
Support coding-related documentation and contribute to the development and maintenance of coding guidelines and SOPs
Participate in system validation, user acceptance testing, and updates related to coding modules and dictionary integrations.
Review and resolve complex or ambiguous verbatim terms, escalating to medical reviewers or clinical teams as needed.
Monitor coding metrics and quality indicators, proactively identifying trends and areas for improvement.
Sourced by ZipRecruiter
11 - 50 Employees
Charlotte, NC, US
2004