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Advanced clinical trials programmer

Uberaba
beBeeClinical
Anunciada dia 18 dezembro
Descrição

Senior Clinical Data Science Programmer

We are seeking an experienced Clinical Data Science Programmer to join our team. As a key member of our data science group, you will be responsible for developing, validating and maintaining programming solutions for clinical trials.

Responsibilities include:
* 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 the integration of programming solutions into the overall data management process.
* Acting as a primary point of contact during the study set up and maintenance phase for system programming related questions by the project team.
* Supporting colleagues with the clinical trials environment and concepts of Clinical Data Management Systems.
* Performing extracts of data from CDMS and creation of data transfer programs.
* Acting as a mentor and providing guidance and support to more junior programmer levels 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.

The ideal candidate will have a strong background in software development, particularly in areas relevant to clinical trials, including data management and statistical analysis. Excellent communication and problem-solving skills are essential for success in this role. We offer competitive salaries and comprehensive benefits packages to successful candidates.

We welcome applications from qualified candidates who can demonstrate the following skills and qualifications:
* Bachelor's degree in Computer Science, Information Technology or related field.
* Minimum 5 years' experience in software development, preferably in clinical trials.
* Strong knowledge of programming languages, including Python, R and SQL.
* Familiarity with CDMS (EDC systems such as Rave/Veeva) and other clinical trial management tools.
* Excellent communication and problem-solving skills.

Affirmative Action Employer. Benefits include:
* Health insurance: Comprehensive medical, dental and vision plans.
* Retirement savings plan: 401(k) plan with employer match.
* Time off: Generous paid time off and holidays.
* Professional development: Opportunities for training and professional growth.

Contact us to discuss this exciting opportunity and learn more about how you can contribute to our dynamic team.

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