Clinical Data Analyst

Job Title: Clinical Data Analyst

Overview:
We are seeking an experienced Clinical Data Analyst to oversee the collection, validation, and analysis of clinical trial data. In this role, you will manage large datasets from various sources, ensure data integrity and compliance, and generate insights through advanced analytical techniques. You will work collaboratively with cross-functional teams to support data-driven decision-making while adhering to regulatory standards.

Key Responsibilities:

• Data Collection & Validation:

  • Collect and validate clinical trial data from multiple sources, including EDC systems, internal databases, and external registries.

• Data Management:

  • Clean, organize, and manage large datasets using appropriate Clinical Data Management (CDM) tools and methodologies.

• Quality Assurance:

  • Perform data reconciliation, manage discrepancies, and conduct quality checks to ensure data integrity and compliance with industry standards.

• Data Analysis:

  • Utilize statistical techniques and tools (e.g., SQL, SAS, Python) to analyze clinical data and extract actionable insights.

• Reporting & Visualization:

  • Develop and maintain reports and dashboards using visualization tools (e.g., Tableau, Power BI) to effectively present data trends to stakeholders.

• Collaboration:

  • Work closely with biostatisticians, data managers, clinical operations, and other cross-functional teams to support data-driven decision-making.

• Regulatory Compliance:

  • Ensure adherence to regulatory standards (e.g., CDISC, FDA, ICH-GCP) and company Standard Operating Procedures (SOPs) for clinical data management.

Qualifications:

• Masters/Bachelor’s degree .
• Proven experience in clinical data management within the pharmaceutical, biotechnology, or healthcare industries.
• Proficiency with data management tools and methodologies specific to clinical data (CDM).
• Strong analytical skills with hands-on experience using SQL, SAS, and Python.
• Experience with data visualization tools such as Excel, Tableau or Power BI.
• Excellent attention to detail with a commitment to maintaining high data quality.
• Effective communication and collaboration skills.

Preferred Skills:

• Familiarity with clinical trial regulatory standards and guidelines (CDISC, FDA, ICH-GCP).
• Ability to manage multiple projects in a dynamic, fast-paced environment.
• Experience working in cross-functional teams to drive data-centric strategies.

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