Senior Manager of Statistics and Database Programming

Responsibilities:

* Prioritize personal workload and that of the group to meet specified completion dates and perform work without direction.
* Ensure good communication across the global management team.
* Demonstrate excellent problem solving skills, a proactive approach and the ability to make sound decisions on a regular basis and communicate these clearly.
* Lead Statistical Programming efforts in the preparation of electronic submissions with good knowledge of the regulatory requirements.
* Lead Statistical Programming efforts in the preparation of electronic submissions with good knowledge of the regulatory requirements.
* Advise on the Technical planning of projects.
* Act as the Biometrics Project Manager or Project Director for assigned projects. This may include global responsibilities.
* Identify and assist others in identifying changes in scope of projects and provide time and cost modifications and detailed information for the development of change orders.
* Provide and interpret resource requirements on a regular basis to ensure that programmers within the department are utilized as fully, but also as efficiently as possible.
* Ensure that resource information is applied across projects to increase utilization, improve efficiency or amend the resource levels required on a project as necessary.
* Assume line management responsibility for a team, conducting performance reviews, setting and regularly reviewing objectives and developing and regularly reviewing training and development plans.

Experience:

* A minimum of 10 years experience in provision of programming support for clinical trial management and reporting, or equivalent experience.
* Strong people management skills and supervisory skills gained from a minimum of 5 years line management experience.
* Extensive experience and proven skills in the use of SAS within a clinical trials environment.
* Extensive experience in all processes / practices used within a Statistical Programming environment.
* Substantial knowledge of all aspects of clinical trials from initial study set-up to study completion.
* Complete knowledge and understanding of the processes and procedures used within a Statistical Programming environment and the ability to communicate to programmers and non-programmers alike.

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