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Clinical Data Analyst Iii

4-6 years
Not Disclosed
10 Jan. 18, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Position: Clinical Data Analyst III
Location: [Location not provided]
Employment Type: [Employment type not specified]
Job Category: [Category not specified]
Job Number: [Job number not provided]
Is Job Remote?: [Remote status not specified]
Country: United States


Job Overview

The Clinical Data Analyst III role is designed for professionals with 4-6 years of experience in clinical data analysis. This position involves more advanced tasks, such as managing large datasets, leading data analysis efforts, and collaborating with cross-functional teams to ensure the successful execution of clinical trials.

Essential Job Responsibilities

  • Oversee the collection, validation, and analysis of clinical trial data, ensuring compliance with protocols, regulatory guidelines, and best practices.
  • Manage the data cleaning and data quality review process to ensure the accuracy and completeness of clinical trial data.
  • Develop and execute data analysis plans, including statistical analyses and the generation of reports.
  • Lead and mentor junior data analysts, providing guidance on best practices for data management and analysis.
  • Support the creation of datasets, tables, and figures for clinical trial reports, presentations, and regulatory submissions.
  • Collaborate with clinical research teams, biostatisticians, and other stakeholders to ensure accurate interpretation and reporting of clinical trial data.
  • Apply knowledge of clinical data standards (e.g., CDISC, SDTM) and work to ensure datasets are consistent with these standards.
  • Conduct root cause analysis and resolve data discrepancies or issues related to clinical data.
  • Support the development and implementation of data management procedures, tools, and systems.
  • Provide expertise in the use of clinical data management software and other analytical tools.

Required Qualifications

  • Bachelor's degree in Life Sciences, Statistics, Computer Science, or a related field.
  • 4-6 years of experience in clinical data analysis, with a proven track record of managing complex clinical trial datasets.
  • Strong understanding of clinical trial design, regulatory requirements, and industry standards (e.g., ICH GCP, CDISC).
  • Advanced proficiency in statistical analysis and data visualization tools (e.g., SAS, R, Python, Excel).
  • Experience with clinical data management systems (CDMS) and familiarity with electronic data capture (EDC) systems.
  • Strong problem-solving skills and the ability to manage multiple priorities and deadlines.
  • Excellent communication and interpersonal skills, with experience working in cross-functional teams.

Preferred Qualifications

  • Master's degree in a related field.
  • Experience in managing and analyzing large clinical trial datasets.
  • Certification in Clinical Data Management or related professional certification.

Additional Information

[Additional company and diversity-related information, if applicable.]