Remote Clinical Data Code, Oncology

Globalchannelmanagement; Marlborough (MA); Remote; USD 90,000 - 120,000; Part time

Job summary

A leading healthcare organization is seeking a Remote Clinical Data Code specialist in Oncology with at least 2 years of experience in clinical data coding, ideally in oncology trials. The position requires a Bachelor's degree in Life Sciences or related fields and strong communication skills for cross-functional collaboration. Responsibilities include ongoing medical coding, resolving coding issues, and maintaining coding listings to comply with standards. Candidates should have a strong understanding of clinical trial data regulations and tools like Rave Coder.

Qualifications

• 2+ years of experience in clinical data coding, preferably in oncology trials.
• Strong understanding of clinical trial data standards and regulatory requirements.
• Excellent attention to detail and ability to manage multiple coding tasks.
• Excellent attention to detail and ability to manage multiple coding tasks in a fast-paced environment.
• Knowledge of ICH, Good Clinical Practice and FDA regulations.
• Proficiency with Rave Coder and familiarity with MedDRA and WHO Drug dictionaries.
• Effective time management and organization skills.
• Strong communication skills for cross-functional collaboration with CRAs, CDMs, and medical reviewers.
• Experience with coding in global, multi-site oncology studies.
• Good interpersonal, written and verbal communication skills.

Responsibilities

• Perform ongoing medical and medication coding using Rave Coder.
• Collaborate with Clinical Data Managers to clarify ambiguous terms.
• Monitor coding metrics and quality indicators for improvement.
• 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.
• Ensure adherence to Data Management standards

Skills

Clinical data coding experience

Attention to detail

Cross-functional collaboration

Knowledge of clinical trial data standards

Familiarity with MedDRA and WHO Drug dictionaries

Education

Bachelor's degree in Life Sciences

Tools

Rave Coder

Job description

Marlborough, Massachusetts, United States

About the job Remote Clinical Data Code, Oncology

Remote Clinical Data Code, Oncology needs 2+ years of experience in clinical data coding, preferably in oncology trials.

Clinical Data Code, Oncology requires:

• 20 hours weekly
• Bachelors degree in Life Sciences, Health Information Management, or related field.
• Strong understanding of clinical trial data standards and regulatory requirements.
• Excellent attention to detail and ability to manage multiple coding tasks in a fast-paced environment.
• Results-driven, take initiative and ownership to accomplish work. Knowledge of ICH, Good Clinical Practice and FDA regulations.
• Proficiency with Rave Coder and familiarity with MedDRA and WHO Drug dictionaries. Effective time management and organization skills.
• Strong communication skills for cross-functional collaboration with CRAs, CDMs, and medical reviewers.
• Experience with coding in global, multi-site oncology studies. Good interpersonal, written and verbal communication skills.

Clinical Data Code, Oncology duties:

• 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.
• Ensure adherence to Data Management standards