Job Opportunity: Senior Clinical Data Science Programmer
We are seeking a skilled and experienced Senior Clinical Data Science Programmer to join our team. This is a fantastic opportunity for an innovative and detail-oriented individual who is passionate about clinical data management.
The successful candidate will have extensive experience in programming for clinical trials, data validation outputs, custom reports, and programs in CDMS (Electronic Data Capture systems such as Rave/Veeva). They will also have strong problem-solving skills, excellent attention to detail, and the ability to work collaboratively in a fast-paced environment.
Responsibilities:
1. 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.
2. Collaborate with data managers, project managers, clinical data scientists, and biostatisticians to ensure the integration of programming solutions into the overall data management process.
3. Act as a primary point of contact during the study set up and maintenance phase for system programming related questions by the project team.
4. Support colleagues with the clinical trials environment and concepts of Clinical Data Management Systems.
5. Perform extracts of data from CDMS and creation of data transfer programs.
6. Act as mentor and provides guidance and support to more junior programmer levels assigned to a project.
7. Assist in the development and implementation of improvements to technical systems and processes within an SME role.
8. Provide guidance on programming best practices, coding standards, and data quality control measures.
9. Stay updated on advancements in programming languages and data management tools to enhance operational efficiencies.
Your Profile:
To be considered for this role, you must have a complete bachelor's degree in a relevant field such as computer science, statistics, or life sciences. You must also have extensive experience in programming for clinical trials, data validation outputs, custom reports, and programs in CDMS (Electronic Data Capture systems such as Rave/Veeva). Additionally, you must have strong problem-solving skills, excellent attention to detail, and the ability to work collaboratively in a fast-paced environment.
Required Skills and Qualifications:
1. Proficiency in programming languages such as SAS, R, or Python.
2. Strong understanding of clinical trial data management principles.
3. Excellent communication and interpersonal skills.
4. MUST HAVE advanced English Communication, Writing and Reading.
icon plc is an equal opportunities employer and welcomes applications from all qualified candidates.
Kindly note that all employees must adhere to icon plc's code of conduct.