Senior Clinical Programmer – Hertfordshire

Paul De Challans is recruiting for a Senior Clinical Programmer to join a pharmaceutical company based in Hertfordshire on a contract basis.

Responsibilities of this clinical job include providing technical coaching and mentoring of DDE standards and guidelines to the Assistant Clinical Programmer, Associate Clinical Programmers and /or Clinical Programmers and to develop and maintain the DDE programming standards, conventions and best practices for the studies in a program.

To apply for this position you must have extensive experience with Clinical Data Management systems, be adapt at programme languages such as SQL, PL/SQL, C# or SAS and be able to implement advanced principles, theories and concepts for one or more sub-functions within CDM.

Click here to apply for this position

 

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Statistical Programmer Job in Paris

Mylene Paumier at CK Clinical is recruiting for a Statistical Programmer to join a Pharmaceutical company at their site based in Paris on a permanent basis.

Statistical Programmer Job Description:

As Statistical Programmer your main responsibilities will be to:

  • Work closely with the Biostatistical department in order to provide technical support for clinical trials. In this context, the candidate could have some clients contacts, but this is not a major part of the job.
  • Write programs for ADs (analysis datasets) based on the SAP (statistical analysis plan),
  • Create programs for tables, figures and listings for the CSR (clinical study report),
  • Perform QC (quality control) of statistical programs,
  • Create tables and figures based on the SAP.

 

Qualifications, Skills and Experience:

As Statistical programmer, you will have the following qualifications, skills and experience:

  • Scientific degree,
  • Extensive SAS knowledge, other statistical software knowledge is a plus,
  • Good knowledge of data mining tools,
  • Good team player,
  • Flexible to work on diverse projects in various disease areas,
  • Good communication skills in English, both written and verbal.
  • Reporting to the Data Management Director Manager.

 

How to Apply:

 

Mylene Paumier at CK Clinical is recruiting for a Statistical Programmer job in Paris

Please contact Mylene for more details.

Click here to apply online now >

For more information or to apply for this Statistical Programmer position, please contact Mylene Paumier on +44 (0)207 470 5672 or email: mpaumier@ckclinical.co.uk. Please quote reference CL24778 in all correspondence.

 

 

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Project Statistical Programmer Job in Europe

Priya Mukherjee at CK Clinical is currently recruiting for a Project Statistical Programmer to join a biopharma leader in Europe.

Project Statistical Programmer Job Description:

As Project Statistical Programmer, you will oversee and manage project related activities for statistical programming activities for the defined development program, including assignment as an associate member of the clinical sub-team.

 

In addition, as the primary Global Statistical Programming representative for assigned development program, you’ll interact with, and serve as primary contact source for clinical team(s) and supporting departments (e.g. Regulatory Affairs, Biostatistics, and Data Management).

Within this Project Statistical Programming role, who will act as lead statistical programmer or support programmer with respect to all statistical programming activities at the Senior Statistical Programmer level and serve as primary GSP contact to respond to questions by regulatory authorities.

In addition, you will communicate and collaborate with the Program Biostatistician to ensure that Statistical Analysis Plans, and other analysis requirements, specifications, or derivation rules are consistent within and across individual studies.

 

 

Qualifications, Skills and Experience:

To be considered for this Project Statistical Programmer position, you will have the following qualifications, skills and experience:

  • A Bachelor’s degree (OR Equivalent) in a Scientific discipline
  • Proven Statistical Programming experience within the Biotechnology and/or Pharmaceutical industry, including clinical research organizations.
  • SAS Software Programming skills equivalent to a Senior Statistical Programmer to solve complex programming tasks according to SDTM and ADaM standard and
  • Advanced understanding of Clinical Trials Design and analysis, together with a basic understanding of integrated summaries of efficacy and safety required for regulatory submissions.
  • A high level of analytical ability, exhibiting characteristics that are structured and methodical to ensure that sound, decisions are made.
  • Be able to plan, perform, trouble-shoot and make decisions based on precedent, company policies, international and national regulations and Good Clinical Practice.

 

How to apply:

 

Priya Mukherjee - Pharmaceutical Recruitment in Europe

Please contact Priya for more details.

Click here to apply online now.

For more information regarding this Project Statistical Programmer position, please contact Priya Mukherjee at CK Clinical on +44 (0)207 470 5670 or email pmukhejree@ckclinical.co.uk. Please quote reference CL24017 in all correspondence.

 

 

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Contract Statistical Programmer Job in Europe

Priya Mukherjee at CK Clinical is recruiting for a contract Statistical Programmer to join a leading pharmaceutical company based in Europe for an initial 6 month contract.

Statistical Programmer Job Description

As Statistical Programmer, you will coordinate, perform and supervise, where appropriate, the programming activities related to project team and departmental deliverables.

 

The core responsibilities of this Statistical Programming job will include:

• Co-ordinate and provide programming input to Project Teams

• Co-ordinate and perform the programming review of database design specifications and Statistical Analysis Plans (SAP)

• Co-ordinate, perform and supervise, where appropriate, the development and validation of trial specific programs for analysis and reporting including the supervision of other programmers, where appropriate

• Co-ordinate and perform the peer review of program code and outputs

• Maintain and archive program documentation, both electronic and paper, in an appropriate manner, including cleaning the project directory

• Assist in improving / developing departmental processes, SOPs and documentation

• Interact with CROs and review their deliverables

• Undertake work according to current operating procedures and guidelines

• Provide programming training, presentations and support to colleagues

• Co-ordinate and develop adequately documented applications

• Provide programming support to the Biostatistics, Data Management and Medical Writing, PK and Clinical Groups

 

Qualifications, Skills and Experience:

To be considered for this contract Statistical Programming position, you will hold an MSc or PhD degree in a Statistics or Mathematics discipline. You should also be familiar with the application of new statistical methods and theories in software solutions involving software like SAS.

 

How to apply:

 

Priya Mukherjee - Programming Recruitment at CK Clinical

Please contact Priya for more details.

Click here to apply online now.

For more information regarding this Statistical Programming position, please contact Priya Mukherjee at CK Clinical on +44 (0)207 470 5670 or email pmukherjee@ckclinical.co.uk.

 

 

 

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Manager of Statistical Programming Job UK

Mylene Paumier is recruiting for a Manager of Statistical Programming to join a global pharmaceutical company at their site based in Hertfordshire on a 6 months contract.

Manager of Statistical Programming Job Description:

The purpose of this Statistical Programming position will be to:

  • Support the Biostatistics team by supporting the computing environment
  • Contribute to the overall efficiency and best practice running of the Biostatistics systems, demonstrating the ability to work efficiently and to a high standard within a clinical team environment

As Manager of Statistical Programming your main responsibilities will include:

  • Overseeing and managing programming activities which may be conducted by external vendors
  • Working with external vendors in order to develop or monitor the content and structure of SAS and related Software installations
  • Developing and maintaining SOPs, SWPs and other related technical documents, providing input and feedback
  • Providing input in developing statistical analysis plans, specifications of analysis datasets, validation plans, and other related documents and determining and researching SAS software upgrades and related system maintenance issues
  • Writing and Executing systems and macro testing (IQ/OQ/UAT), and delivering training.

Qualifications, Skills and Experience:

As Manager of Statistical Programming, you will have the following qualifications, skills and experience:

  • Bachelor’s degree in Statistics, Computer Science, Mathematics, or a related science discipline preferred (Masters degree preferred)
  • Experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment
  • Some management experience in a pharmaceutical/CRO programming environment or demonstrated significant leadership of SAS programming activities in a clinical pharmaceutical/CRO environment
  • Validation and Systems Development Life Cycle
  • Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. Proven experience with Unix and Windows operating systems
  • Understanding of FDA guidelines.
  • Hands-on experience with industry tools including biostatistics platforms, ETL, standard reporting and visualization tools (e.g. Base SAS, SAS CDI, SAS Data Miner, JMP, SAS DD, Oracle HLS, Oracle CDC/Waban, Informatica, Business Objects, i/J Review, Spotfire)

How to apply:

Mylene Paumier - Statistical Programming Recruitment at CK Clinical

Please contact Mylene for more details.

Click here to apply online now.

For more information regarding this this Manager of Statistical Programming position, please contact Mylene Paumier on 01438 743047 or email: mpaumier@ckclinical.co.uk. Please quote reference CL24401 in all correspondence.

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