|
Page 1
|
| Novartis Oncology |
na |
NJ |
7/31/2010
|
| Sr Biostatistician |
| Typically requires a Master's Degree in Statistics with at least 3 years of related experience. Typical entry level with Ph.D. in Statistics. To be considered for this level, demonstrated proficiency in the following skills and responsibilities are required: With supervision, apply advanced statistical/programming and/or PK/PD modeling in the preparation of CSRs, manuscripts, ISSs, and ISEs that meet world-wide health authority and medical community standards, and participate in protocol preparation. |
| Novartis Oncology |
na |
NJ |
7/31/2010
|
| Sr Principal Biostatistician |
| Education Minimum/desirable): At least Masters Degree in Statistics (or equivalent degree with five years of experience or PhD with 2-3 years of experience.
Languages: Fluent English (oral or written).
Experience/Professional requirements:
1. Experience in all tasks of a Trial Statistician.
2. Proven knowledge in Statistics and its applications to clinical trials.
3. Proven knowledge of drug development and HA guidelines. Background medical knowledge preferably in relation to the specific therapeutic area.
4. Proven knowledge of statistical software packages.
5. Good communication and presentation skills.
6. Good team player |
| Novartis Oncology |
na |
NJ |
7/31/2010
|
| Sr Principal Biostatistician |
| At least Masters Degree in Statistics (or equivalent degree) with 5 years of experience or PhD with 2-3 years of experience.
Fluent English (oral or written)
1. Experience in all tasks of a Trial Statistician.
2. Proven knowledge in Statistics and its applications to clinical trials.
3. Proven knowledge of drug development and HA guidelines. Background medical knowledge, preferably in relation to the specific therapeutic area.
4. Proven knowledge of statistical software packages.
5. Good communication and presentation skills.
6. Good team player. |
| Novartis Oncology |
na |
MA |
7/31/2010
|
| Sr. Biostatistician |
| Education Minimum/desirable): At least Masters Degree in Statistics (or equivalent degree with five years of experience or PhD with 2-3 years of experience.
Languages: Fluent English (oral or written).
Experience/Professional requirements:
1. Experience in all tasks of a Trial Statistician.
2. Proven knowledge in Statistics and its applications to clinical trials.
3. Proven knowledge of drug development and HA guidelines. Background medical knowledge preferably in relation to the specific therapeutic area.
4. Proven knowledge of statistical software packages.
5. Good communication and presentation skills.
6. Good team player. |
| Novartis Oncology |
na |
NJ |
7/31/2010
|
| Sr Biostatistician |
| Education (minimum/desirable): At least Masters Degree in Statistics (or equivalent degree) with 7 years of experience or PhD with 4 years of experience.
Languages: Fluent English (oral and written).
Experience/Professional requirements:
1. Experience gained in the main tasks of program statistician (about 2-4 years).
2. Proven knowledge and expertise in statistics and its applications to clinical trials in at least one TA. Solid 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 Programmers.
8. Good team player. Good business ethics.
9. Good leadership skills. |
| Novartis Oncology |
na |
MA |
7/31/2010
|
| Biostatistician, Biomarker Analysis |
| The successful candidate will have a Ph.D. degree in Biostatistics or Statistics with > 5 years experience in statistical analysis, including at least 4 years experience in the analysis of high-dimensional biomarker data preferably in a pharmaceutical setting. A strong background in parametric and nonparametric statistical methods, multivariate statistics, classification and resampling, as well as experience in analysis of biomarker and assay data is required. Experience in predictive modeling, classification and discriminant analysis is also desirable. The candidate should possess strong communication skills with the ability to communicate effectively with statisticians and non-statisticians alike. Experience with R/Bioconductor, SAS and other relevant software packages is a must. Familiarity with a Linux/Unix environment will be a plus. Strong scientific writing skills, collaborative skills and multitasking skills are all key attributes required for this position. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
7/30/2010
|
| Temp. Sr. Biostatistician |
| * At least 5 years direct experience in the pharmaceutical industry.
* Masters, Ph.D preferred.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Astellas Pharma, Inc. |
Deerfield |
IL |
7/30/2010
|
| Associate Biostatistics Director, Oncology |
| M.S. or Ph.D. in statistics or equivalentMinimum of 8 years experience in applying statistical methods in biomedical research, extensive pharmaceutical or CRO experience requiredExperience in working on clinical project teams. Good understanding of entire drug development process - ability to see the ?big picture?.Experience as the independent lead statistician in a regulatory submission preferredExperience with cross functional process improvement or innovation initiativesAdvanced and broad knowledge of statistical methods, along with understanding of industry practices related to the statistical analysis of clinical dataKnowledge and skills in SAS required and knowledge of other statistical software preferred.In-depth familiarity with processes and procedures in data management and SAS programmingExperience working in an international environment and demonstrated ability to manage and influence across different locations, time zones and cultures; builds global relationships. Ability to work in a matrix environment. Proven excellent organizational, project and time management skills.Leadership skills and ability to delegate appropriately and provide direction to more junior Biostatisticians. Very good oral, written, and presentation communication skills. Able to clearly communicate statistical issues and methods to both statisticians and non-statisticians. Very good problem solving skills.Accurate with a keen eye for detail. Dedication to quality and reliability in all work tasksAbility to perform under pressure |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
7/30/2010
|
| Staff Biostatistician |
| Education/Experience Qualified candidates must have Statistics, Biostatistics, or Mathematics: MS or PhD. PhD + 8 yrs or MS + 10 years of pharmaceutical industry experience; full knowledge of advanced statistical analytical methods, clinical trial research, regulatory requirements, coding techniques, and statistical software. Excellent oral and written communication skills; project planning skills; demonstrated experience in analyzing clinical trial data; priority setting skills; multi-tasking skills; problem solving skills; eye for detail; exercise good judgment; and works well within team framework. Comprehensive project management skills. Demonstrated competency in SAS. Regular attendance at IDT Meetings is necessary; experience in managing CROs and external vendors. |
|
Page 1
|
