R&D Programmer
Date: Jun 22, 2022
Location: Netanya, IL, 11111
Company: Teva Pharmaceuticals
Company Info
Job Description
The Clinical Programming Manager is responsible to manage the timely and accurate execution of programming components of clinical trials.
The Manager leads and manages completed projects, that involved global tasks or cross functional teams or outsourcing resources. The role may require providing inputs to design and analysis, and report the results of clinical trials including programming rules and mocked T/L/G; In addition, providing all safety claims for new drugs and extension of claims/publication support for our marketed drugs.
Qualifications
Education Required: Bachelor's or higher degree in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
Experience Required: More than 7 years of professional experience in pharmaceutical or clinical research.
Specialized or Technical Knowledge Licenses, Certifications needed:
Excellent SAS knowledge of the following SAS modules/procedures: Base SAS; SAS report writing; SAS macros/functions.
Job-Specific Competencies:
1. Good oral and written communication skills in English
2. Interpersonal communication skills
3. Ability to effectively work in a global environment
4. Ability to effectively interact with and influence others without direct reporting relationships
5. Professional accuracy and integrity
6. Ability to work under pressure and in a multitasking environment
7. Innovation driven and open for a change
Function
Sub Function
Reports To
Assoc Dir Clinical Programming, Clinical Programming
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