Dear Allstat,
Please find below our latest permanent statistics opportunity.
Our clients based in the South East are actively looking for an experienced
statistician with an Oncology background to come on board as a lead project
statistician. There is an excellent package for the right candidates with
flexible benefits and competitive remuneration.
If this position could be of interest to you please send an updated CV to
[log in to unmask] or alternatively you can reach me on +44 (0)207
922 7126
JOB DESCRIPTION
The Project Statistician at this level will provide statistical support in
multiple dimensions including:
- provides technical leadership and expertise to execute multi-disciplinary
or cross functional projects that will influence the Research Laboratory and
the Statistical Science organization;
- leads the assessment and introduction of new statistical technology and
methodology to apply to broader practice;
- leads or assists in the development of clinical plans, protocol designs,
and statistical analysis plans in collaboration with physicians and/or
medical colleagues
- provides consulting on priority clinical projects, appropriate technical
oversight and coaching
Key Objectives
The job tasks listed below outline the scope of the position. The
application of these tasks may vary, based upon current business needs.
Statistical Knowledge and Expertise
• Perform research and develop methodologies, especially in modeling and
simulation and other innovative statistical approaches
• Stay current with respect to statistical methodology, to maintain
proficiency in applying new and varied methods, and to be competent in
justifying methods selected.
• Develop approaches or solutions that save time, increase efficiency or
otherwise directly impact business
• Operate in collaboration with study personnel to provide input on study
protocol, design studies and write protocols for the conduct of each study.
• Assist in or be accountable for selecting statistical methods for data
analysis, authoring the corresponding sections of the protocol, and
conducting the actual analysis once a reporting database is created.
• Participate in peer-review work products from other statistical
colleagues, and advise others on technical aspects.
Communication, Leadership and Influence
• Defines or adjusts project objectives to reflect broader strategy and
objectives.
• Can effectively lead cross-functional or multi-disciplinary groups and use
technical expertise to influence business decisions.
• Collaborate with team members to write reports and communicate results.
• Assist with, or be responsible for, communicating study results via
manuscripts, or oral presentations in group settings, as well as for
communicating one-on-one with key customers and presenting at scientific
meetings.
• Respond to regulatory queries and to interact with regulators.
Pharmaceutical Industry/Therapeutic Area Knowledge
• Have broad understanding about the drug hunting process across phases
• Understand disease states in order to enhance the level of customer focus
and collaboration and be seen as a strong scientific contributor.
Regulatory Compliance
• Perform 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.
Additional Preferences
• Deep knowledge of the drug development process (phase I-IV)
• Experience in modeling and simulation
• Interpersonal communication skills for effective customer consultation
• Teamwork and leadership skills
• Self-management skills with a focus on results for timely and accurate
completion of competing deliverables
• Resource management skills
• Creativity and innovation
• Demonstrated problem solving ability and strategic thinking
• Business process expertise associated with critical activities (e.g.
regulatory submissions)
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