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Clinical Trial Associate

1-3 years
Not Disclosed
15 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

Job Details

 

Clinical Data Management (CDM) Job Description

Clinical Data Managers (CDMs) are responsible for ensuring the accuracy, integrity, and completeness of data collected in clinical trials. They work closely with clinical investigators, statisticians, and other members of the clinical trial team to develop and implement data management plans, design and maintain clinical databases, and review and analyze data. CDMs play a critical role in ensuring that clinical trials are conducted efficiently and that the data collected is reliable and trustworthy.

Responsibilities

Qualifications

 

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    • Develop and implement data management plans, including data collection, entry, cleaning, and analysis procedures.

    • Design and maintain clinical databases to ensure the efficient and secure collection and storage of data.

    • Review and analyze data to identify trends, outliers, and inconsistencies.

    • Work with clinical investigators to resolve data discrepancies and ensure that all data is collected and recorded accurately.

    • Prepare reports and presentations on clinical trial data.

    • Stay up-to-date on regulatory requirements and best practices in clinical data management.

      • Bachelor's degree in a related field, such as statistics, computer science, or healthcare administration

      • Master's degree in clinical data management or a related field is preferred

      • Experience with clinical data management software and databases

      • Strong understanding of regulatory requirements and best practices in clinical data management

      • Excellent analytical and problem-solving skills

      • Strong written and verbal communication skills

    • Ability to work independently and as part of a team

Other Details