Hello all

 

Below is a list of Jobs for your perusal, please email or phone me directly if interested in any of these are of interest. Please bear in mind these are just some of the roles I have available. I would be more than happy to have an informal discussion with anyone interested. 

 

If you are not available or interested but may know someone who is, then please take advantage of our recommendation scheme, where we give £500 (in vouchers of your choice) if we successfully place the person you recommended (see our website for full details).

 

Thanks again, and if this is not relevant to you please accept my apologies in advance.

 

Urgent Vacancies:

 

1 year contract: Phase 1 trial Statistician – South West Germany

 

Background information: 

The candidate will work in the Phase1_2a biostatistics team and be responsible for planning and analysing Clinical Pharmacology studies. Typical study types are Bioequivalence, Bioavailability (Drug, drug Interaction, Drug, Food Interaction, Drug, Formulation BA studies), Single Rising Dose, Multiple Rising Dose etc.

 

Scope of work:

The candidate will act as a fully responsible trial statistician.

He/she will collaborate with the Clinical Pharmacologist, Clinical Kineticist, Data Manager and SAS Programmer. For non-complex trials, the analysis and reporting may be contracted out to specialized CRO’s, while for complex trials, analysis and reporting is done in-house involving SAS Programmers to execute the Trial Statistical Analysis Plan (TSAP). For report writing, a medical writer is also involved.

 

As usual in Phase 1, standard specifications (TSAP, tables, graphs & listings) and analysis tools (SAS macros for BA/BE/dose proportionality) are available to handle routine tasks efficiently. 

 

Qualification:

MSc or PhD in statistics or math. At least 2 years experience working as a statistician in on Clinical Pharmacology studies a Pharma company / CRO. Excellent general biostatistics knowledge. Good knowledge about pharmacology and kinetics. Good communication skills.

 

 

1 year contract - Phase 3 trial Statistician – South West Germany

 

Background information: 

The candidate will work in the Clinical Biostatistics Team and be responsible to support the preparation, conduct and reporting of phase 3 trials in the respiratory area. The candidate will work closely together with the Project Statistician. Additional interfaces are to the other members of the trial team (Trial Manager, Data Manager and SAS Programmer) and the project team (Project Data Manager, the Project Statistical Programmer). 

 

Scope of work:

The candidate will act as a fully responsible trial statistician and will support the Project Statistician.

 

In the early study conduct phase, main tasks are the definition and review of data quality checks and the review of statistical issues during study conduct. Thereafter, the preparation of specifications for analysis and reporting has to be created. A prototype Trial Statistical Analysis Plan for the entire phase 3 program of the compound has to be written and corresponding SAS programs and outputs have to be discussed and QC'd.  Statistical standards for the projects have to be reviewed.

 

Depending on the scope of work the candidate may also work as a fully responsible trial statistician for phase 2/3 trials in the diabetes area. 

 

Qualification:

MSc or PhD in statistics or math. At least 2 years experience working on phase 2/3 studies in a Pharma company / CRO. Excellent general biostatistics knowledge. Good communication skills.

 

 

Other current vacancies:

 

 

MRS193 - Senior Statistical Programmers (SAS)

1 Year Contract – Northern Germany – Negotiable rate

 

MRS189 - SAS Programmer (SAS)

Perm – Switz – salary negotiable + relocation + Package

 

MRS191 – Clinical Data Manager

Perm – Switz - salary negotiable + relocation + Package

 

MRS190 – Biostatistician 

1 Year Contract – Switz – Good CHF rate + rent + flights

 

MRS185 – Biostatistician

1 Year Contract – Southern Germany - €Negotiable rate 

 

MRS193 - Senior Statistical Programmers (SAS)

1 Year Contract – Southern Germany – €Negotiable rate

 

MRS31 – Senior SAS Programmer (SAS)

Permanent – Surrey - to £40,000 + package

 

MRS52 – 4x Senior Clinical Data Project Manager

1 Year Contract – N of London – Negotiable rate 

 

MRS29 – Clinical Data Manager

Permanent – Switz – salary negotiable + relocation + Package

 

MRS17 – Principle Statistician

Permanent – Holland – salary to €100,000 + Package + relocation

 

MRS51 - Team Leader, Data Management

Permanent - Holland – salary to €80,000 + Package + relocation

 

MRS60 – Senior Clinical Statistician

Permanent - Holland – salary to €80,000 + package + relocation

 

MRS194 – 4 x Senior Statistical Programmers (SAS)

Permanent - Germany - salary to €70,000 + package + relocation 

 

I also have a number of vacancies all over the UK for Clinical Data Managers, Statisticians and SAS Programmers, so if you don’t see anything above that interests you, please give me a ring as these are just some of the vacancies that I am currently recruiting for.

 

Kind regards

 

Marc

 

 

Marc R Saunders

Managing Director

 

The Avocet Partnership

2nd Floor

4 Broadgate Circle

London EC2M 2QS

 

Tel:  +44 (0) 207 965 4619

Mob: +44 (0) 787 2621226

Fax:  +44 (0) 207 965 4630

Email:  <mailto:[log in to unmask]> [log in to unmask]

Website: www.avocetpartnership.com

 

P Please consider the environment before printing this email