Ref #: 30633

Employment type: Permanent - Full-Time

Location: China-Shanghai

Posted: 13-Jul-2021

Description

Services Overview: Complete programming activities including development, verification, and documentation of various complexity in support of clinical reporting and submissions.
Deliverables:
• Services rendered will adhere to applicable Johnson & Johnson SOPs, WIs, policies, local regulatory requirements, etc.
• Designs and develops statistical programs in support of clinical research analysis and reporting activities.
• Performs quality control in support of clinical research analysis and reporting activities.
• Maintains documentation as appropriate.
• Completes programming tasks of low to medium complexity with high quality and timeliness of deliverables.
• If applicable, region specific deliverables will be specified.
• Advanced:
o Completes programming tasks of medium to high complexity with high quality and timeliness of deliverables.
o Critically reviews requirements and data, identifies gaps, suggests solutions, and applies expertise to improve efficiency of programming tasks and/or improve overall quality of programming deliverables.

Metrics/KPIs: Metrics/KPIs governing these services are outlined in the Quality Oversight Plan (QOP) document.

Interfaces – Primary/Other:
• Primary interfaces: N/A
• Other Interfaces: N/A

Education and Experience Requirements:
• Bachelor’s degree or higher and/or equivalent in computer science, mathematics or other scientific field (or equivalent theoretical/technical depth).
• 2 years programming experience, preferably in a pharmaceutical/Clinical R&D environment.
• Demonstrated written and verbal communications skills. Proficiency in written and spoken English.
• Experience working with programmers in a team environment preferred.
• Advanced:
o Five years programming experience with increasing responsibility, preferably in a pharmaceutical/Clinical R&D environment.
o Knowledge of programming language(s) and data structures. “