Teva Associate Director Statistical Programming 

United States, Pennsylvania, East Bradford Township 

105090901

1. Clinical trials production systems management and business processes improvement

It is in Clinical Programming’s long term best interest to retain SAS technical expertise in house. As the cloud gradually replaces Teva data center over the next few years and clinical trials processing shifts to the cloud entirely, there will undoubtedly be many new challenges that require innovation and creativity. A proven technical expert grounded in Clinical Programming’s current processes will best serve this role. As time goes by, the team can grow to have additional members who will share the knowledge and responsibilities, thus enhancing technical stability for Clinical Programming.

2. Development of new technologies and tools

3. Cross-functional support of other teams

4. Vision for future growth

Education Required:

• Bachelor's or higher degree in Science, Statistics, Iinformation Technology or equivalent combination of education and related work experience.

Experience Required:

⦁ More than 13 years of professional experience in pharmaceutical or clinical research.

Experience Preferred:

⦁ Specialized or Technical Knowledge Licenses, Certifications needed:Excellent SAS knowledge of the following SAS modules/ procedures: Base SAS; SAS report writing; SAS macros\ functions.

Functional Knowledge:

Job-Specific Competencies:

⦁ Good oral and written communication skills in English.
⦁ Interpersonal communications skills.
⦁ Ability to effectively work in a global environment.
⦁ Ability to effectively interact with and influence others without direct reporting relationships
⦁ Professional accuracy and integrity
⦁ Ability to work under pressure and in a multitask environment.
⦁ Innovation driven and open for a change.

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