CK Clinical has been asked by a global biotech company to help them recruit 3 Senior Associate, Biostatical Programmers to join their team on a permanent basis.

 

With supervision, your main responsibility will be to write, test and validate software programs to support the analysis and presentation of biomedical data ensuring quality and accuracy of programming deliverables and adherence to the company's Policies, SOPs and other controlled documents.

 

The key responsibilities of the Senior Associate Biostatical Programmer are to:

• Assist in the review of key study-related documents produced by other functions, e.g. case report form, data management plan, NONMEM specifications

•Write, test and validate software programs in Unix to produce analysis datasets and presentation output, to be included in reports for submission to regulatory agencies, publications and other communications

•Understand and execute department-, product- and study-level macros and utilities

•Write, test and validate product- and study-level macros and utilities

•Assist with study and systems audits by Clinical Quality Assurance (CQA) and external bodies, and respond to audit questions and findings

•Provide input to and participate in intra-departmental and GBDS meetings

•Contribute to the continuous improvement of Global Biomedical Data Sciences (GBDS) and programming

•Assist in the review of GBDS policies, standard operating procedures and other controlled documents

•Provide support to and mentor more junior programmers

•Interface with outsourcing partners and vendors

•Attend external professional organizations, conferences, training and/or meetings

 

As a Senior Associate Biostatical Programmer, the following  basic qualifications, skills and experience are required:

·Bachelors degree

·General clinical research and development programming experience

·Statistical programming  experience in SAS within the drug development setting using the SAS System version 9.1.3 or higher

 

As a Senior Associate Biostatical Programmer, the following  preferred qualifications, skills and experience are required:

·Bachelors or Masters degree, in Computer Science, Statistics, Mathematics, Life Sciences or other relevant scientific subject

·General clinical research and development programming experience

·Drug Development (pre-, early, late and/or observational) in related industries or academic research

·SAS programming expertise in the BASE, STAT, GRAPH, Macro and SQL modules.

·Proven clinical research and development programming experience (including working to CDISC standards, SDTM and ADaM) and the ability to work effectively within a globally dispersed team.

 

For this position, Knowledge of the following is needed:

·Computer programming, preferably SAS or other procedural languages

·Understanding of computer operating systems, UNIX preferred

·Fundamentals of Project Planning and Management

·Drug Development Process & Operations

 

For more information or to apply for the Senior Associate Biostatical Programmer role, please contact Jessica Todd on 01438 842976 or email [log in to unmask]

 

Jessica Todd BA
Trainee Consultant - Biometrics
CK Clinical Limited
9 High Street
Stevenage
SG1 3BG
DD: 01438 842976
T: 01438 743047
F: 01438 723800
W: www.ckclinical.co.uk / www.ckmedics.com

 

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