Clinical Data Programmer @ Clin Biosciences

Job Description

 You are responsible for developing, implementing, and maintaining clinical trial databases and related programming tasks. This includes tasks such as designing, programming, and validating clinical databases, generating data listings and reports, and ensuring data quality and integrity. They also play a crucial role in data integration from various sources, including external data, and ensuring compliance with relevant regulations and guidelines. 

Responsibilities:

• • Database Development and Maintenance: Designing, developing, testing, and maintaining clinical databases, often using Rave and SAS.   
  • Data Integration: Collaborating with cross-functional teams to integrate electronic data capture (EDC) systems with CRFs.   
  • Data Extraction and Reporting: Developing and utilizing complex SQL queries to extract data from large datasets for analysis and reporting.   
  • Custom Application Development: Utilizing programming languages like C# to build custom applications for data manipulation and visualization.   
  • Regulatory Compliance: Ensuring compliance with regulatory requirements, including implementing and maintaining catalog management processes. 

Qualifications:

• Masters/Bachelors degree in Life Sciences or a related field.
• 0- 2+ years of experience in clinical data management.
• Strong proficiency in Medidata Rave.
• Excellent knowledge of GCP and 21 CFR Part 11.
• Strong attention to detail and problem-solving skills.
• Specialized courses or certifications in Clinical Data Management can be beneficial. 

Interested to apply can share CV or call/whatsapp to hidden_mobile

 

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Keyskills:   pharmacovigilance data analysis argus safety clinical data management