ClinChoice is seeking a highly skilled Senior/Principal Statistical Programmer Consultant with a focus on oncology to join our dynamic team. This role offers the opportunity to work directly with a single sponsor while benefiting from the resources and career advancement opportunities of a global Contract Research Organization (CRO). You will play a key role in delivering high-quality programming support for clinical studies, ensuring that all deliverables meet industry standards.
| Basic Details | |
|---|---|
| Experience | 1 - 2 Years |
| Location | Kuwait |
| Qualification | Mentioned Below |
| Benefits: | Mentioned Below |
| Posted | |
| Job Type | Full-Time |
| Posted by | Hamna (Senior HR) |
| last date to apply | apply within 15 days of posting |
This blog post will break down everything you need to know about the position, from the typical tasks to the qualifications and how to contact the employer.
Responsibilities
Programming Deliverables:
- Support programming deliveries for clinical studies and projects, ensuring high quality and efficiency.
- Implement statistical programming components of protocols and clinical development programs.
Quality Assurance:
- Ensure quality is embedded in your own deliverables and in the outputs of other programmers.
- Write and implement specifications, overseeing the completeness of all relevant documentation.
Best Practices Development:
- Contribute to the development of best practices to enhance quality, efficiency, and effectiveness within the programming function.
- Ensure compliance with relevant standards and automation protocols.
Team Collaboration:
- Plan and support team activities, communicating and escalating risks within assigned studies.
- Collaborate proactively with study team members, including Statisticians, Lead Programmers, Data Managers, and Study Leaders.
Qualifications
Education:
- Bachelor’s degree in Computer Science, Statistics, or a related scientific discipline with at least 5 years of clinical programming (CDISC) experience, or
- Master’s degree in the same fields with a minimum of 6 years of clinical programming (CDISC) experience.
Experience:
- Required experience in Oncology therapeutic area.
- Strong working knowledge of ICH guidelines, Good Clinical Practices, clinical research processes, and relevant regulatory requirements.
Skills:
- Excellent communication and coordination skills.
- Current knowledge of technical and regulatory requirements related to statistical programming.
- Proven ability to manage multiple concurrent activities effectively.
Key Competencies
- Strong analytical and problem-solving skills
- Attention to detail
- Proficiency in statistical programming languages (e.g., SAS, R)
- Ability to influence and collaborate with stakeholders
- Adaptability and flexibility in a fast-paced environment
Benefits
- Career Growth: Opportunities for professional development within a global CRO.
- Collaborative Culture: Work in a supportive environment that values teamwork and individual contributions.
- Competitive Compensation: Attractive remuneration packages aligned with industry standards.
Application Instructions
If you are excited about this opportunity and meet the qualifications, please submit the following:
- Your updated CV
- A cover letter detailing your relevant experience and motivation for applying
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