Senior Biostatistician - Pharma

Key Accountabilities:

- Provide advise and expertise in statistical methods and techniques to internal Statisticians and Programmers.

- Represent Biostatistics

- Participate in business development.

- Act as key contact regarding customer relationship management activities.

- Establish and maintain sound working relationships and effective communication with Clients and global Early Phase biostatistical group.

- Organise and participate in Client and team meetings.

- Identify and facilitate training needs in collaboration with Line Managers.

- Manage quality issues.

- Monitor productivity.

- Participate in preparation of audits / inspections, audits and any follow up activities.

- Awareness of Revenue Recognition and associated tasks and timelines.

- Effectively communicate with internal and external customers as well as third party vendors.

- Prioritise effectively and respond to urgent requests within internal group and the Client.

Skills:

- Experience in all tasks of a Trial Statistician.

- Proven knowledge in Statistics and its applications to clinical trials.

- Proven knowledge of statistical software packages.

- Good communication and presentation skills.

- Possess strong negotiation, diplomacy, team leadership skills and excellent organizational ability.

- Excellent interpersonal, verbal and written communication skills.

- Ability to identify and address issues proactively in a timely manner.

- Ability to make appropriate decisions in ambiguous situations.

- Carefully weighs the priority of project tasks and directs team accordingly.

- Excellent computer literacy.

- Demonstrate a sound knowledge of all relevant regulations, including GCP.

- Good team player.

Education:

- A Ph.D. degree or equivalent in statistical science, mathematical analysis or related field plus 4 years relevant experience or a master's degree plus 6 years relevant experience.

- Comprehensive knowledge of statistical theory and methods and demonstrated ability to apply it to all phases of clinical trials.

- Expertise in SAS programming including statistical analysis, data manipulation and scientific graphing.