Clinical Data Lead

3 semanas atrás

Curitiba, Brasil beBeeClinicalData Tempo inteiro

Lead Clinical Data Programmer Role About the Job: We are seeking a highly skilled Clinical Data Programmer to join our team. The successful candidate will be responsible for developing, validating, and maintaining programming solutions for clinical trials. The ideal candidate will have extensive experience in programming for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials with proficiency in languages such as SAS, R, or Python. Key Responsibilities: - Develop, validate, and maintain programming solutions for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials. - Collaborate with data managers, project managers, clinical data scientists, and biostatisticians to ensure the integration of programming solutions into the overall data management process. - Act as a primary point of contact during the study set up and maintenance phase for system programming related questions by the project team. - Support colleagues with the clinical trials environment and concepts of Clinical Data Management Systems. - Perform extracts of data from CDMS and creation of data transfer programs. - Act as mentor and provides guidance and support to more junior programmer levels assigned to a project. - Assist in the development and implementation of improvements to technical systems and processes within an SME role. - Provide guidance on programming best practices, coding standards, and data quality control measures. - Stay updated on advancements in programming languages and data management tools to enhance operational efficiencies. Required Skills and Qualifications: - Bachelor's degree in a relevant field, such as computer science, SAS, statistics, or life sciences. - Extensive experience in programming for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials with proficiency in languages such as SAS, R, or Python. - Strong problem-solving skills and the ability to work collaboratively in a fast-paced, cross-functional environment. - Excellent attention to detail and organizational skills, with a commitment to delivering high-quality results. - Strong communication and interpersonal skills, with the ability to effectively collaborate with diverse teams and influence outcomes. - Advanced English Communication, Writing, and Reading skills are required. What We Offer: - Competitive salary and benefits package. - Opportunities for professional growth and development. - Collaborative and dynamic work environment. How to Apply: Please submit your application, including your resume and cover letter, to us.

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