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Clinical Data Analyst Iii

4-6 years
Not Disclosed
10 Jan. 23, 2025
Job Description
Job Type: Full Time Education: B.Sc, M.Sc, B.Pharm, M.Pharm, LifeScience Graduates 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

Job Title: Clinical Data Analyst III

Experience Required: 4 – 6 Years

Location: [Specify Location]

Job Description:

We are looking for an experienced and skilled Clinical Data Analyst III to join our team. The ideal candidate will have 4 to 6 years of experience in clinical data analysis, with a strong background in managing and interpreting clinical trial data. As a Clinical Data Analyst III, you will play a key role in ensuring the accuracy, integrity, and quality of clinical trial data, supporting decision-making processes and ensuring compliance with regulatory requirements.

Key Responsibilities:

  • Analyze and interpret clinical trial data to ensure its accuracy, completeness, and consistency.
  • Review, validate, and clean data from clinical trials to identify and resolve discrepancies, ensuring high-quality data.
  • Work closely with clinical research teams to provide insights and recommendations based on data analysis to support study objectives.
  • Develop and implement data management plans, ensuring that data collection, processing, and reporting follow industry standards and regulatory guidelines (e.g., ICH-GCP).
  • Oversee and mentor junior data analysts, providing guidance and training on best practices in data analysis.
  • Prepare and deliver reports, presentations, and datasets for internal teams, sponsors, and regulatory bodies.
  • Ensure compliance with data privacy regulations, industry standards, and sponsor-specific requirements.
  • Collaborate with cross-functional teams, including clinical operations, biostatistics, and regulatory, to ensure alignment and support of clinical trial goals.
  • Participate in the development of data analysis strategies, processes, and tools to enhance data management efficiency.
  • Lead and support the setup, maintenance, and troubleshooting of data management systems and databases.

Qualifications:

  • Bachelor’s or Master’s degree in Life Sciences, Statistics, Healthcare, or a related field.
  • 4-6 years of experience in clinical data analysis or clinical data management, with a solid understanding of clinical trial processes.
  • Proficiency in statistical analysis software (e.g., SAS, R) and data management tools (e.g., EDC, CTMS).
  • Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial data management best practices.
  • Experience in leading data analysis projects and mentoring junior team members.
  • Exceptional attention to detail and ability to handle large datasets with accuracy.
  • Excellent communication and presentation skills, with the ability to effectively communicate complex data findings to cross-functional teams.
  • Strong problem-solving abilities and ability to resolve data-related issues proactively.
  • Ability to work effectively in a team-oriented environment and manage multiple priorities.

This is an exciting opportunity for a seasoned Clinical Data Analyst to advance their career and make a significant impact on clinical trial data management. If you have a passion for data integrity and want to contribute to the success of clinical research, we encourage you to apply.

Rush your CVs to : careers@clinztech.com