Senior Clinical Programming Lead
7 days ago
The opportunity at Teva Pharma
Job SummaryWe are seeking a skilled Clinical Programming Manager to join our team. As a key member of our global clinical operations group, you will be responsible for managing the timely and accurate execution of programming components of clinical trials.
About the RoleThis is a senior leadership role that requires strong technical expertise, excellent communication skills, and the ability to work collaboratively with cross-functional teams. The ideal candidate will have a deep understanding of clinical trial methodology and regulatory requirements, as well as experience with data management systems and statistical analysis software.
- Provide input for budget planning
- Oversee contingent workers and/or vendors
- Provide training to others
The successful candidate will have a strong background in computer science, statistics, or a related field, and will be able to develop, review, and perform validation of generic macros. Experience with CDISC guidelines and requirements is highly desirable.
Your QualificationsTo be considered for this role, you will need:
- Bachelor's Degree/ Master's Degree/ PhD in Science, Statistics, Information Technology or equivalent combination of education and related work experience
- Bachelor's + 5 years or Master's + 4 years of professional experience in a pharmaceutical or clinical research setting as a programmer
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