Senior Specialist Programmer-ONCO - Early Phase
at ClinChoice
Hill, England, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 04 Jul, 2024 | Not Specified | 04 Apr, 2024 | N/A | Regulatory Requirements,Communication Skills,Clinical Practices,Coordination Skills,Computer Science,Statistics,Terminology,Cs,Clinical Research | No | No |
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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 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 client’s counterparts.
EDUCATION AND EXPERIENCE:
- 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
Responsibilities:
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.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Computer science (cs statistics or related scientific disciplines with 5 yrs
Proficient
1
Hill, United Kingdom