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Senior clinical data science programmer - remote opportunity

Anápolis
beBeeClinical
Anunciada dia 18 dezembro
Descrição

Job Opportunity for Senior Clinical Data Scientist

We are seeking a highly skilled and experienced Senior Clinical Data Scientist to join our team.

This is a remote position based in Brazil, working with us on various projects across the globe. You will play a key role in developing and implementing programming solutions to support the analysis and reporting of clinical trial data.

You will contribute to the advancement of innovative treatments and therapies by ensuring the accuracy and efficiency of data processing through your expertise.

What You Will Be Doing:

* Developing, validating, and maintaining 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.
* Collaborating with data managers, project managers, clinical data scientists, and biostatisticians to ensure integration into the overall data management process.
* Acting as primary point of contact during study set up and maintenance phase for system programming related questions from the project team.
* Supporting colleagues with clinical trials environment and concepts of Clinical Data Management Systems.
* Performing extracts of data from CDMS and creation of data transfer programs.
* Acting as mentor and providing guidance and support to junior programmers assigned to a project.
* Assisting in the development and implementation of improvements to technical systems and processes within an SME role.
* Providing guidance on programming best practices, coding standards, and data quality control measures.
* Staying updated on advancements in programming languages and data management tools to enhance operational efficiencies.

Requirements:

* A bachelor's degree 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 ability to work collaboratively in fast-paced environment.
* Excellent attention to detail and organizational skills, with a commitment to delivering high-quality results.
* Strong communication and interpersonal skills, with ability to effectively collaborate with diverse teams and influence outcomes.
* MUST HAVE advanced English Communication, Writing and Reading.

About Us:

Our company is a world-leading healthcare intelligence and clinical research organization dedicated to fostering an inclusive environment driving innovation and excellence.

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