
Senior/Principal Statistical Programmer Consultant-ONCOLOGY-REMOTE@EMEA
ClinChoice
Employment Type
Full Time
Location
Dubai
Experience
Senior
Required Skills
Job Description
Description Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds. ClinChoice is searching for a Senior/Principal Statistical Programmer 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 client’s counterparts.
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.
Requirements
- Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience; Master’s degree in CS, statistics or related disciplines with 6 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.
About the Company ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.
How to Apply
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