Pharmaceutical Data Analyst - Clinical Trials

Placements24; Benoni; Hybrid; ZAR 420,000 - 600,000; Full time

Benefits offered by this job

Medical aid

Retirement fund

Professional development

Hybrid work model

Job summary

Placements24 recruits a Pharmaceutical Data Analyst in Benoni, Gauteng to support clinical trial operations. You will manage, process, and analyze data from studies, ensuring integrity and timely reporting.

Collaborate with clinical operations, biostatisticians and data managers; develop databases; contribute to regulatory submissions, all within a hybrid work model.

Qualifications

• Bachelor's degree in a quantitative field.
• Minimum of 3 years in data analysis or data management.
• Proficiency in SAS, R or SPSS.
• Experience with SQL databases and clinical data.
• Knowledge of clinical trial processes and GCP is a plus.

Responsibilities

• Collect, clean, validate, and manage clinical trial data from various sources.
• Perform data analysis to identify trends and insights.
• Develop and maintain databases for trial information.
• Prepare reports and visualizations for stakeholders and submissions.
• Collaborate with clinical teams to define data requirements and quality.
• Resolve data discrepancies and ensure adherence to SOPs and ICH GCP.
• Assist in EDc systems and CRF development as needed.
• Support audits, inspections, and data-related meetings.
• Contribute to continuous improvement of data management processes.

Skills

Data analysis

Data management

Analytical skills

Attention to detail

Communication

Education

Bachelor's degree in Statistics/Mathematics/CS

Tools

SAS

R

SPSS

SQL

Job description

About the Role

Our client, a leading pharmaceutical research organization, is seeking a skilled and analytical Pharmaceutical Data Analyst to support their clinical trial operations in **Benoni, Gauteng**. This role is essential for managing, processing, and analyzing the vast amounts of data generated during clinical studies. You will work closely with clinical operations teams, biostatisticians, and data managers to ensure data integrity, accuracy, and timely reporting. The ideal candidate will possess strong data management and analytical skills, proficiency in relevant software, and a solid understanding of clinical trial processes. This hybrid position combines in-office responsibilities with remote flexibility, offering a balanced work environment in the **Benoni** area.

Key Responsibilities

• Collect, clean, validate, and manage clinical trial data from various sources.
• Perform data analysis using statistical software to identify trends, patterns, and insights.
• Develop and maintain databases and data management systems for clinical trial information.
• Prepare reports and visualizations of clinical trial data for internal stakeholders and regulatory submissions.
• Collaborate with clinical teams to define data requirements and ensure data quality.
• Identify and resolve data discrepancies and inconsistencies.
• Ensure adherence to data management plans, standard operating procedures (SOPs), and regulatory guidelines (e.g., ICH GCP).
• Assist in the development of Case Report Forms (CRFs) and electronic data capture (EDC) systems.
• Support data review meetings and provide data-related support for audits and inspections.
• Contribute to the continuous improvement of data management processes and tools.

Requirements

• Bachelor's degree in Statistics, Mathematics, Computer Science, Bioinformatics, or a related quantitative field.
• Minimum of 3 years of experience in data analysis or data management, preferably within the pharmaceutical or clinical research industry.
• Proficiency in statistical software such as SAS, R, or SPSS.
• Experience with database management systems (e.g., SQL).
• Familiarity with clinical trial processes and terminology.
• Strong understanding of data quality principles and validation techniques.
• Excellent analytical and problem-solving skills with high attention to detail.
• Effective written and verbal communication skills.
• Ability to work independently and collaboratively within a team environment.
• Experience with EDC systems (e.g., Medidata Rave, Oracle Clinical) is a plus.

Benefits

• Our client offers a competitive salary, comprehensive medical aid, and retirement fund benefits.
• Opportunities for professional development and further training in data science and clinical research are provided.
• The hybrid work model offers flexibility, promoting a healthy work-life balance.

Join a dedicated team focused on advancing medical research and patient care in **Benoni, Gauteng**, with ample opportunities for career growth within a reputable pharmaceutical organization.