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Clinical Data Analyst I

0-1 years
Not Disclosed
12 June 14, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, 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

Must have 6 months to 1 year of experience in Clinical data managment.

Data Validation (cleaning):

  • Responsible for/start to lead data cleaning and data review activities (Co-Primary CDA/Primary CDA), e.g. query management and manual/SAS listing reviews.

  • Support/start to lead data processing activities from database setup to database lock, e.g. external vendor data reconciliation.

Data Management Documents/Plans (Trial Master File):

  • Perform and/or support the setup of DM documents and ensure proper documentation as per Standard Operating Procedures, ICH/GCP Guidelines.

Study Start-Up Activities and User Acceptance Testing (UAT):

  • Start to lead/perform user acceptance testing on clinical database setups.

  • Start to review protocols and EDC Entry Screens if required.

Data Tracking and Entry:

  • Track and review CRFs. Support data entry where required.

Project Quality Management & Compliance:

  • Ensure compliance to Standard Operating Procedures, ICH/GCP Guidelines.

  • Support/start to lead functional QC activities on databases and/or patient data, as per business needs.

Training:

  • Maintain training compliance as per Job Roles assigned, including On-the-Job training.

  • Address training needs, as per Development Goal/s identified.

Skills:

  • Evidence of strong problem-solving skills and logical reasoning

  • Commitment to first time quality, including a methodical, analytical and accurate approach to work activities (attention to detail)

  • Time management and prioritization skills in order to meet objectives and timelines

  • Evidence of ability to work collaboratively within a team environment

  • Good interpersonal, oral and written communication skills

  • Learning ability and knowledge sharing approach; swift understanding of technologies and new processes

  • A flexible attitude with respect to work assignments and new learning; ability to adjust rapidly to changing technical environments

  • Evidence of accountability relative to Key Accountabilities in Job Description

  • Written and oral fluency in English


Knowledge and Experience:

  • Demonstrates technical aptitude with awareness/potential prior experience in Microsoft Office Products (basic computer skills).

  • Basic understanding of data management processes and data validation flow (e.g. Data cleaning, DB lock)

  • Basic understanding of relevant ICH-GCP Guidelines, local regulatory requirements and PAREXEL SOPs and study specific procedures

  • Basic knowledge of Clinical Data Management Systems (e.g. InForm, Rave, Veeva, Datalabs, ClinBase.)

  • Basic understanding of Clinical Study Team roles within Data Management

  • Experience in clinical research industry

  • Basic knowledge of medical terminology and coding dictionaries (e.g. MedDRA & WHODRUG)

  • Basic knowledge of Data Management Operational processes and tasks during study start-up, conduct and close-out

  • Basic knowledge of Database set-up activities, including but not limited to Database Configuration Specifications and setup of Data Validation

Education:

  • Bachelor’s degree and/or other medical qualifications or relevant industry experience.