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Clinical Data Analyst I

0-2 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 I
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 I role is suited for individuals with 0-2 years of experience in clinical data analysis. This entry-level position involves assisting in the management, analysis, and reporting of clinical trial data to support the development of medical products.

Essential Job Responsibilities

  • Assist in the collection, validation, and analysis of clinical trial data.
  • Maintain and ensure the accuracy of clinical data according to protocol and regulatory requirements.
  • Support data management activities, including data cleaning and preparation for analysis.
  • Assist in the preparation of reports, including summary statistics and visualizations.
  • Collaborate with team members to ensure timely and accurate completion of project tasks.
  • Learn and apply clinical data standards and guidelines (e.g., CDISC, SDTM).
  • Perform basic data queries and assist in resolving data discrepancies.
  • Provide support to senior data analysts and data managers in all phases of clinical trials.

Required Qualifications

  • Bachelor's degree in Life Sciences, Statistics, Computer Science, or a related field.
  • 0-2 years of experience in clinical data analysis or related field.
  • Strong attention to detail and organizational skills.
  • Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).
  • Basic understanding of clinical trial processes and regulatory requirements.
  • Ability to work independently and as part of a team.
  • Good communication skills, both written and verbal.

Preferred Qualifications

  • Familiarity with clinical data management software and database systems.
  • Knowledge of clinical data standards such as CDISC or SDTM.

Additional Information

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