Job Description
Our organization is seeking a highly skilled Clinical Data Science Programmer to play a pivotal role in developing and implementing programming solutions for clinical trials. As part of our diverse and dynamic team, you will contribute to the advancement of innovative treatments and therapies by ensuring the accuracy and efficiency of data processing through your expertise.
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 primary point of contact during study setup and maintenance phases for system programming-related questions from the project team.
* Support colleagues with clinical trial environments and concepts of Clinical Data Management Systems.
* Perform extracts of data from CDMS and create data transfer programs.
* Act as mentor and provide guidance and support to 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 & Qualifications
* Hold a bachelor's degree in a relevant field, such as computer science, statistics, or life sciences.
* 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 like SAS, R, or Python.
* Demonstrate strong problem-solving skills and ability to work collaboratively in fast-paced cross-functional environments.
* Exhibit excellent attention to detail and organizational skills with a commitment to delivering high-quality results.
* Display strong communication and interpersonal skills, with the ability to effectively collaborate with diverse teams and influence outcomes.
* Must have advanced English communication, writing, and reading skills.
What You Will Be Doing:
* Work on developing, validating, and maintaining programming solutions for various aspects of clinical trials.
* Collaborate with stakeholders to integrate programming solutions into the overall data management process.
* Be the primary point of contact for system programming-related questions from the project team.
* Support colleagues with their understanding of clinical trial environments and Clinical Data Management Systems.
* Extract data from CDMS and create data transfer programs.
* Mentor junior programmers and provide guidance and support.
* Assist in improving technical systems and processes within the SME role.
* Advise on programming best practices, coding standards, and data quality control measures.
* Stay up-to-date on advancements in programming languages and data management tools to improve operational efficiency.
Your Profile:
* Have a bachelor's degree in a relevant field.
* Hold extensive experience in programming for clinical trials with proficiency in languages like SAS, R, or Python.
* Possess strong problem-solving skills and the ability to work collaboratively in a fast-paced environment.
* Exhibit excellent attention to detail and organizational skills.
* Display strong communication and interpersonal skills.
* Have advanced English communication, writing, and reading skills.