About the job Principal/Senior Statistical Programmer-ONCO
ClinChoice is searching for a Principal/Statistical Programmer Analyst/Consultant to join one of our clients.ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the clients counterparts.
Main Job Tasks and Responsibilities:The Senior Statistical Programmer Analyst/Consultant is a delivery-focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the programming effort to deliver technical programming and information components of a project. This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks
Key Responsibilities:
- Responsible for supporting the Programming deliveries of a clinical study or project.
- Implements statistical programming aspects of the protocol and the clinical development program.
- Ensures high quality is built into own deliverables and the quality delivered by other programmers.
- Programs independently with high efficiency and quality.
- Writes and/or implements specifications and oversees completeness of relevant documentation.
- Contribute to the development of best practices to improve quality, efficiency, and effectiveness within the function.
- Ensures compliance with standards and automation usage.
- Plans and support team activities and tasks.
- Communicates and escalates risks within the assigned studies and/or projects.
- Works proactively with study team members including but not limited to the Statistician, Lead Programmer, Data Manager and Study Leader.
Education and Experience:
- Bachelors degree in computer science (CS), statistics, or related scientific disciplines with 6 yrs. of clinical programming (CDISC) experience; Masters degree in CS, statistics or related disciplines with 7 yrs. of clinical programming (CDISC) experience.
- Need to have Oncology TA experience.
- Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology.
- Good understanding of the clinical drug development process.
- Strong communication skills and coordination skills.
- Current knowledge of technical and regulatory requirements relevant for the role
- Ability to proactively manage concurrent activities within a project
- Proficient ability to influence relevant stakeholders on programming-related items.
Please use the below link for job application and quicker response.
https://lifelancer.com/jobs/view/e564dcd55e0ce8d95f8482af4d7eb60c