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Job Details

SAS Programmer – Glasgow, UK

Company: Clintec
Location: Glasgow, UK
Reference: UK-SAS-221117-MC
Closing Date: 19 Mar 18
Type: Full Time
Salary (£): Competitive
Benefits:

Job Summary:

ClinTec International is actively recruiting for a SAS Programmer to join our expanding global company in in the UK – Permanent contract, opportunity. By working for ClinTec you can further your career in a dynamic, fast-paced environment and you can be assured of rewarding benefits.

Requirements:

ClinTec International is actively recruiting for a SAS Programmer to join our expanding global company in in the UK – Permanent contract, opportunity. By working for ClinTec you can further your career in a dynamic, fast-paced environment and you can be assured of rewarding benefits.

 

Role Description

A SAS Programmer will be expected to lead and/or support programming activities and produce associated documentation involved in reporting of clinical trials in accordance with the protocol, standard operating procedures (SOPs), good clinical practices (GCP) and other applicable regulatory requirements.  They will be leading and/or support the specification, programming and documentation of SDTM and ADaM datasets and generation and validation of Tables, Listings and Figures for individual studies and study programmes.

As a technical expert, they will be expected to support relevant internal and external users for CDISC compliance and documentation.  Where appropriate, mentoring and support of junior SAS programming staff, peers and other department staff is expected.

 

Key Accountabilities

  • Responsible for leading and/or supporting SAS Programming across multiple clinical trials
  • Produce SDTM and ADaM datasets, tables, listings and figures
  • Generate and maintain required specification and documentation
  • Review data management planning documentation, such as data management plan, edit check specifications, data transfer agreements
  • Proactively provide process improvement feedback to Management and provide input in SOP updates/development
  • Participate in audits as required
  • Assist in business development activities as required
  • Assist in developing programming related timelines
  • Assists in addressing external application vendor issues, integrations, and implementations
  • Collaborate with clients (as and when required), peers, project teams and/or requestors to clarify and finalise specifications
  • Maintain and continue to gain a broad overall knowledge in the field of clinical programming and clinical data management

 

Company Information:

Clintec is a dynamic, UK headquartered, privately owned, full service Contract Research Organisation with a presence in over 50 countries worldwide. We have been providing clinical research support services to clients in the pharmaceutical, biotechnology and medical device industries and assisting in their key product development efforts for over two decades. At Clintec we have experience in managing clinical trials in all major therapeutic areas including oncology, rare disease, neurology, cardiovascular, psychiatry, infectious disease, rheumatology, immunology, respiratory and gastroenterology.

Clintec employees can expect to receive expert training and guidance throughout their careers as well as the opportunity to be involved in every aspect of Clinical Trials across the full life-cycle of the drug development process from the CRO perspective. We have strong partnerships with some of the world's leading pharmaceutical companies and employees can expect to be involved in some of the most prestigious drug development projects with the opportunity to develop, progress and travel globally. Clintec offers a competitive salary and rewards package.

Apply for this job: SAS Programmer – Glasgow, UK

Contact Information:

Address:  Head Office
Clintec International Ltd,
133 Finnieston Street,
Glasgow
G3 8HB
Scotland
Reasons to work for Clintec
Tel:  +44 (0) 141 226 1120
Fax:  +44 (0) 141 248 8993
Website:  Visit Our Web Site

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