Head of Biostatistcs

Summary about this job

Detail information about job Head of Biostatistcs. Terms and conditions vacancy

• Strategic Leadership Role
• Customer-Focused Full service Contract Research Organisation (CRO)
• Full time , 12 months contract role, based in Sydney office

About Us
At GreenLight Clinical we strongly believe that effective healthcare is enabling. Translating innovative discoveries, through clinical development, into novel and accessible medical therapies is fundamental to achieving better health outcomes for patients. We favour customised strategies, often adopting cutting edge technology-based solutions, and we thoughtfully integrate our capabilities with the existing strengths of our partners to achieve smarter, faster results. We guarantee the highest quality standards in clinical research, conducted within an ethically rigorous framework.

About the Role

We are currently seeking an innovative and highly experienced Executive Biostatistician to provide strategic leadership and guidance as the statistical expert to multiple project teams.

Reporting to the CEO, in this role you will be accountable for all statistical aspects of clinical studies and submissions, including quality, relevance to regulatory perspective, and scientific validity.  You will oversee the execution of statistical analysis and the preparation of the statistical methods and results sections for clinical study reports (CSR) and production of overall summaries. You will collaborate with clinical and regulatory leads in defining general strategic approach, creating clinical development plans (CDP) and producing individual protocols.

About You
In order to be considered for this role, you will possess the following Position Requirements (Selection Criteria):

• PH.D. (MS) in statistics or related discipline
• 10+ years of pharmaceutical experience, including significant interactions with regulatory bodies, history of successful management (4+ years), and expertise in one or more therapeutic areas
• Broad knowledge and superior understanding of advanced statistical concepts and techniques
• In- depth understanding of the regulatory drug submission / approval process regionally and globally
• Superior level verbal, writing, and presentation skills with the demonstrated ability to effectively represent Biostatistics and Programming in multidisciplinary or cross-functional meetings
• Proven leadership, project management, and interpersonal skills
• Experience managing direct reports, assembling teams, and implementing working relationships with external agencies, such as CRO, consultant groups, and research committees
• Innovatively applies technical principles, theories, and concepts to pharmaceutical clinical development and life cycle management

We offer

• The opportunity to be part of a growing organisation that values their staff
• A collegial and collaborative working environment
• A chance to make a difference and enable effective healthcare for individuals and the communities they live in

Would you like to know more?

To learn more about GreenLight Clinical, please visit our website http://www.greenlightclinical.com   

To obtain a copy of the position description which details more of the role accountabilities, you are welcome to contact [email protected]

About Applying

To apply for this role, please send your application to [email protected]  by 5.00pm AEST 19 July 2018.

Applications must specify residency or work visa status, include your CV and a Cover Letter which includes responses to the Selection Criteria detailed in the position description.

Greenlight Clinical is an EEO employer and values diversity. We encourage applications from people of diverse cultures, gender and ages.

The personal data collected will be used for recruitment purposes only. We reserve the right to conduct police checks and other screening procedures prior to employment being confirmed.