Key Roles and Responsibilities:
* We are seeking a senior programmer to develop, validate, and maintain programming solutions for clinical trials data management systems.
* The selected candidate will collaborate with cross-functional teams to ensure integration of programming solutions into the overall data management process.
* The primary responsibilities include 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, and acting as mentor and providing guidance and support to more junior programmer levels assigned to a project.
Our ideal candidate has:
* A bachelor's degree in a relevant field such as computer science, statistics, or life sciences.
* Extensive experience in programming for clinical trials data management systems, 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, ability to work collaboratively in a fast-paced environment, excellent attention to detail and organizational skills, with commitment to delivering high-quality results.
* Strong communication and interpersonal skills, with ability to effectively collaborate with diverse teams and influence outcomes.
Responsibilities Include:
* Data Programming: Develop, validate, and maintain programming solutions for CDMS, data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials.
* Collaboration: Collaborate with data managers, project managers, clinical data scientists, and biostatisticians to ensure integration of programming solutions into the overall data management process.
* Mentorship: Act as mentor and provide guidance and support to more junior programmer levels assigned to a project.
Requirements:
* Bachelor's degree in a relevant field such as computer science, statistics, or life sciences.
* Extensive experience in programming for clinical trials data management systems, 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 a fast-paced environment.
Benefits:
* Opportunity to work on complex projects and contribute to the development of clinical trials data management systems.
* Collaborative and dynamic work environment.
* Professional growth and development opportunities.