Expert Statistician Oncology. 

One of largest Pharma companies in the world are looking for an experienced
Statistician to join their Oncology business. Within this role you would be
the statistical leader and project manager for all B&SR deliverables
globally for a clinical development program, or a mega trial. 

Amongst other responsibilities, you will ensure that clinical development
program (or parts assigned) meets scientific,regulatory, quality, and
commercialization requirements, through interaction with the IPT and ICT,
perform matrix management of B&SR project team, and mentor staff as
required. You will also ensure ECD-Bios, and modeling and simulation
contribution is fully integrated into the project. 

SKILLS & EXPERIENCE:

At least Masters Degree in Statistics (or equivalent degree) 
Languages: 
Fluent English (oral and written) 

Experience/Professional requirement: 
1. Experience gained in the main tasks of a program statistician 
2. Proven knowledge and expertise in statistics and its applications to
clinical trials in at least one TA. Solid knowledge and experience in drug
development process and HA guidelines. 
3. Background medical knowledge, preferably in relation to the specific
therapeutic area. 
4. Good knowledge of statistical software packages. 
5. Very good project management skills. 
6. Very good communication and presentation skills. 
7. Ability to give effective guidance to Trial Statisticians and Program
Programmer. 
8. Good team player Good business ethics. 
9. Good leadership skills.

Please forward CV's to [log in to unmask] for immediate review. 




Senior Statistical Programmer

This is an exciting opportunity for an experienced Statistician to join one
of the globe's largest and reputable Pharma companies. Within this role, you
will be responsible for all statistical tasks on the assigned clinical
trials; may be assigned to lead a small project or parts (e.g. indication);
track clinical trial/allocated project activities and milestones; ensure
timeliness and adequate quality of all deliverables for the assigned trials
and project tasks; Follow processes and adhere to Novartis and project
specific standards as well as Health Authority requirements (SOPs, Master
Analysis Plan, GCP, and regulatory guidelines); Participate in or lead
non-clinical project activities as needed; Establish and maintain sound
working relationships and effective communication within the Clinical Trial
Team/International Clinical Team and the Biostatistics team. 

Fluent English (oral or written).
Experience in all tasks of a Trial Statistician.
Proven knowledge in Statistics and its applications to clinical trials.
Proven knowledge of drug development and HA guidelines. Background medical
knowledge, preferably in relation to the specific therapeutic area.
Proven knowledge of statistical software packages.
Good communication and presentation skills. 
Good team player. 


Please forward CV's to [log in to unmask] for immediate review. 


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