Job Description

Schedule: 100%Duration: 6- 12 month contractStart Date: ASAPLocation: India (Fully Remote)Contract Type: Freelance/ContractLanguages Required: EnglishI am partnered with a Global CRO, who are currently seeking a Contract Statistical Programmer to join their team. You will play a pivotal role within the team as you will be the lead for the study. You will be responsible for programming and validating statistical analysis datasets, tables, listings, and figures according to study protocols and statistical analysis plans and be This is a great opportunity to work with a dynamic team and contribute to the success of their projects.

• Effectively designs and codes SAS programs for assigned project(s), consistently meeting objectives of the project
• Produce and deliver CDISC and regulatory compliant SDTM, and ADaM standard datasets
• Demonstrates advanced experience with all SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH
• Demonstrates advanced knowledge of electronic submissions (eSub) and CDlSC
• Create and validate tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements
• Provide input in the design and development of case report forms and clinical databases
• Perform quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs
• Review or author SDTM and ADaM datasets specifications for datasets programming
• Provide programming support for ad-hoc analysis
• Identify problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group (e.g., macros or graphical user interface applications)
• Manage timelines and schedules of specific phases of projects with internal personnel and external vendors.
• Review or validate statistical deliverables of vendors for assigned project(s)
• Responsible for maintaining excellent working knowledge of medical data, the design and phases of clinical trials, statistics, relevant regulatory requirements, and the pharmaceutical industry
• Displays highly advanced knowledge regarding software validation and system development life cycle concepts

By clicking \xe2\x80\x9capply\xe2\x80\x9d you will be sending your CV to Elysabeth Yates at AL Solutions. Elysabeth is a specialist Senior recruiter within Biometrics, HEOR & Market Access. She will discuss the opportunity in detail with you, facilitate your application and will manage the process acting as a link between the company and yourself. Due to the interesting nature of this position, it is likely that recruitment could close prematurely due to a high number of expected applicants. Please call +44 203 778 0909 for more information or reach out to Elysabeth Yates directly on elysabeth@alsolutions.co.uk with the link to the job advert.Requirements

• Bachelor\xe2\x80\x99s Degree in Statistics, Mathematics, Computer Science, Life Sciences or other relevant scientific fields; Master\xe2\x80\x99s Degree preferred.
• Minimum of 5-6 years of experience in developing statistical programming deliverables for clinical trials using SAS, R and or Python coding.
• Good knowledge of statistics and Oncology/Neuroscience drug development process.
• Proven record of effective and successful project management tasks and skills.
• Communicates effectively in verbal presentations and written technical reports to both internal and external customers

AL Solutions