Job Description

Position: Principal Statistical Programmer Analyst/Consultant
Employment type: 12 Month Contract - Extendable
Location: REMOTE

About ClinChoice

ClinChoice is a global CRO dedicated to offering high-quality one-stop service to biopharmaceutical, medical device, and consumer products clients. Some of these services include clinical operations, project management, biostatistics, data management, regulatory affairs, medical affairs, and pharmacovigilance. ClinChoice has established major delivery centers across US, Canada, China, Europe, India, Japan, and the Philippines. It has over 3,000 employees globally, with a strong and talented team, and a growing clinical operations presence in seven countries across Asia, North America, and Europe.

Summary

The Principal Statistical Programmer Analyst/Consultant is accountable for quality, timely and efficient delivery of project, programming work and good information management. This position requires profound programming experience and excellent industry knowledge to independently lead implementation of programming activities as well as lead other programmers. It is a leadership role that can have a project or technical focus It will provide subject matter expertise within the Programming discipline. As an expert within their own field, acts as a specialist within cross-functional teams to deliver continuous improvement.

Responsibilities

• Leads and directs the full scope of project delivery and/or leads a technical project within the TA/Drug Project/study/function
• Leads Implementation of statistical programming aspects of the protocol or clinical development program
• Responsible for the high quality of all project deliverables, holding partners and providers accountable for the quality of their deliverable and/or technical subject matter expert for aspect(s) of the TA, Project, or function
• Leads or contribute to cross-functional administrative or process improvement initiative(s)
• Drives the development of best practices to improve quality, efficiency and/or effectiveness within the function
• Drives standards development and implementation
• Manages and escalate risk in complicated or novel situations within their study and/or projects
• Provides Programming expertise to the team
• Provides tactical input and/or drives ideas and improvements
• Contributes to the function by supporting recruiting and/or providing training and mentorship
• Identifies opportunities to improve methodology and provides practical solutions for problems
• Influences stakeholders by providing subject matter expertise on programming related items
• Ensures compliance to standards and automation usage
• Employs all project management practices in managing drug or technical projects
• Provides input to capacity management for all projects in scope
• Maintains expertise of the latest industry and regulatory requirements to stay current

Qualifications and Experience

• Bachelor’s degree in computer science (CS), statistics or related scientific disciplines with 8 yrs. clinical programming experience; Master’s degree in CS, statistics or related disciplines with 7yrs. of clinical programming experience.
• Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology.
• Good understanding of clinical drug development process.
• Detail oriented.
• Strong communication skills and coordination skills.
• Can communicate with global team independently.

Confidential for Review Purposes Only

• 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
• Ability to manage risk in complicated or novel situations
• Project Mindset

Clinchoice is an Equal opportunity Employer/committed to diversity

Job Types: Full-time, Temporary contract

Pay: £25.00-£30.00 per hour

Schedule:

• 8 hour shift
• Monday to Friday

Education:

• Bachelor's (preferred)

Experience:

• SAS: 3 years (required)
• Clinical trials: 3 years (required)

Work Location: Remote

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