Dear Allstat,
Please find below details of our latest opportunity for our client recruiting for a Study Statistician to be based in their office in the South East of England.
As a Study Statistician, you will lead and provide oversight in the development of study protocols and data analysis plans in collaboration with physicians, and/or medical colleagues. The Study Statistician will be responsible for working with research associates and scientists to oversee the establishment of a reporting database and the analyses of study data. Furthermore, the Project Statistician will lead the study team on their interpretation of results and will be co-author for internal or external publication of the results.
Further responsibilities of the Study Statistician position, involving the Statistical Study Design and Analysis (Phase I-IV clinical trials or observational studies) will include:
•Operates in collaboration with study personnel to provide input on study protocol and design of studies.
•Writes statistical parts of protocols for clinical trials and / or observational studies.
•Assists in or is accountable for selecting statistical methods for data analysis.
•Collaborates with data management in the planning and implementation of data quality assurance plans.
•Maintains currency with respect to statistical methodology, to maintain proficiency in applying new and varied methods, and is competent in justifying methods selected.
•Participates in peer-reviewing work products from other statistical colleagues.
•Supports medical affairs in the statistical aspects of designing, implementation and results interpretation of patient support programs.
•Communication of Results and Inferences
•Collaborates with team members to write reports and communicate results.
•Assists with or is responsible for communicating study results via regulatory submissions, manuscripts, or oral presentations in group settings, as well as presenting at scientific meetings.
•Performs work in full compliance with assigned curriculum(s) and will be responsible for following applicable Corporate, Medical, local, and departmental policies, procedures, processes, and training.
As a Study Statistician, you will have the following qualifications, skills and experience:
•A PhD, or a Masters degree in a statistics based subject.
•Good knowledge of pharmaceutical industry processes and procedures.
•An understanding of clinical data, including data quality issues.
If you are interested in further details please contact me directly at [log in to unmask]
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