Data Analyst - Clinical Trials

Placements24

Pretoria

Hybrid

ZAR 480,000 - 720,000

Full time

6 days ago
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Job summary

Placements24 is seeking a skilled Data Analyst focused on Clinical Trials to join its research division. This fully remote role allows you to manage and analyze complex trial data from Pretoria-based operations, supporting drug development and research validation.

You will generate insights, ensure data integrity, and collaborate with cross-functional teams in a virtual environment, contributing to our programs' success.

Qualifications

  • Bachelor's or Master's in Statistics, Biostatistics, Bioinformatics, Data Science, or related field.
  • Minimum of 3 years as a Data Analyst with focus on clinical trial data management/analysis.
  • Proficiency in SAS, R, or Python for statistical analysis.

Responsibilities

  • Collect, clean, and validate large clinical trial datasets to ensure accuracy and regulatory compliance.
  • Perform statistical analysis to identify trends, efficacy, and safety signals using SAS/R/Python.
  • Develop data dictionaries, data management plans, and SOPs for clinical data.
  • Create reports, visualizations, and dashboards for project teams and regulatory bodies.
  • Collaborate with clinical operations, biostatistics, and medical affairs to define data requirements and analytics strategies.
  • Identify data anomalies and implement corrective actions to maintain data quality.

Skills

Data analysis
Statistical analysis
Remote collaboration
Data visualization

Education

Bachelor's or Master's in Statistics/BIo/DS
Master's degree preferred

Tools

SAS
R
Python
Tableau
Power BI

Job description

About the Role

Our client is looking for a skilled Data Analyst with a focus on Clinical Trials to join their innovative research division, operating remotely from Pretoria . This critical role involves managing, analyzing, and interpreting complex clinical trial data to support drug development and research validation. You will play a key part in ensuring data integrity, generating insights, and contributing to the overall success of our clinical research programs. This fully remote position requires a proactive individual with exceptional analytical abilities and a keen eye for detail, who can effectively collaborate with cross-functional teams in a virtual setting.

Key Responsibilities
  • Collect, clean, and validate large datasets generated from clinical trials, ensuring accuracy and compliance with regulatory standards.
  • Perform statistical analysis on clinical trial data using appropriate software (e.g., SAS, R, Python) to identify trends, efficacy, and safety signals.
  • Develop and maintain data dictionaries, data management plans, and standard operating procedures (SOPs) for clinical data.
  • Create clear and concise reports, visualizations, and dashboards to present findings to project teams, stakeholders, and regulatory bodies.
  • Collaborate with clinical operations, biostatistics, and medical affairs teams to define data requirements and analytical strategies.
  • Identify and investigate data anomalies, implementing corrective actions as needed to maintain data quality.
Requirements
  • Bachelor's or Master's degree in Statistics, Biostatistics, Bioinformatics, Data Science, or a related quantitative field.
  • Minimum of 3 years of experience as a Data Analyst, with a significant focus on clinical trial data management and analysis.
  • Proficiency in statistical analysis software such as SAS , R, or Python.
  • Strong understanding of clinical trial phases, data types, and regulatory requirements (e.g., ICH-GCP, FDA guidelines).
  • Excellent data visualization skills and experience with tools like Tableau or Power BI.
  • Proven ability to work independently and manage multiple projects effectively in a remote environment.
Benefits
  • Competitive annual salary and performance-related bonuses.
  • Comprehensive health, dental, and vision insurance.
  • Flexible remote working arrangements enabling work-life balance.
  • Opportunities for professional growth and development in a fast-paced research setting.
  • Collaborative virtual environment with a focus on scientific advancement.
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