Clinical Programmer II (EMEA)

£0.00 - £65 per hour
  1. Contract
  2. Program Manager / Director
  3. United Kingdom
London
Posting date: 15 Aug 2019
SS.TM.24889_1565864102

A leading global contract research organisation is seeking to recruit a Clinical Programmer II (EMEA). The company provides comprehensive, integrated drug development, laboratory, and lifecycle management services, working with partners across pharmaceutical, biotechnology, medical device, academic, and government organizations. This is an exciting opportunity to work with a company that has offices in 48 countries and more than 20,000 professionals worldwide, with a commitment to quality to help clients and partners bend the cost and time curve of drug development to deliver life-changing therapies that improve health.

Job Responsibilities:

  • Database position working with clinical trials data systems under general supervision.
  • Provides technical leadership for some or all of the following activities.
  • Designs and implements global library and study specific setup for clinical trials applications; develops and validates data checks.
  • Provides first-line end user support/problem solving; provides support for application validation activities.

Skills and Requirements:

  • Bachelor's degree in computer science, statistics, biostatistics, mathematics, biology, or other
  • health related field, or equivalent experience that provides the skills and knowledge necessary to
  • perform the job.
  • Minimum of 2 years of experience in a clinical trials environment or similar field.
  • Minimum of 1 year of experience with Oracle or similar applications in a programming or administration capacity.
  • OC/RDC experience preferred.
  • Minimum of 1 year of experience with Medidata Rave and/or Rave certification.
  • Knowledge of relational database systems (RDBMS) and structure
  • Experience in Oracle and with Oracle tools or similar, with working knowledge of SQL and/or
  • PLSQL.
  • Demonstrated experience in identification and resolution of technical problems in a professional environment
  • Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data.
  • Ability to attain, maintain, and apply a working knowledge of GCPs and applicable SOPs.
  • Demonstrable multitasking, project management, and execution skills.
  • Good interpersonal skills, including communication, presentation, persuasion, and influence.
  • Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
  • Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Tom Magenis at +44 203 854 1050 or upload your CV on our website - www.proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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