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Clinical Data Programmer (SAS)

od 4Create (Bilo gde)

PRIMARY RESPONSIBILITIES

Provides data to clients (internal and external) in functional format by:

  • Creating and executing SAS edit check programs
  • Validating edit check programs using standard validation practices and processes
  • Creating, validating and executing SAS programs and macros
  • Utilizing SAS programming skills to provide ad-hoc reports (external and internal)
  • Assist in developing programming specifications
  • Assist in creating program specific validation plans
  • Identifying and implementing solutions for complex reporting needs

Ensures client data accuracy and integrity by:

  • Creating and/or reviewing data editing and export specifications
  • Working directly with clinical data manager, and where needed with clinical project manager and other team
    members to ensure specifications are clear and accurate.
  • Has a clear understanding of the contextual requirements for reporting outputs; and provides feedback
  • Programming data cleaning/consistency checking programs to support internal applications for all
    therapeutic areas
  • Programming and testing data export programs in accordance with specific client needs
  • Documenting all programming and validation efforts in accordance with Good Clinical Practices
  • Monitoring data integrity throughout a given study
  • Utilizing SDTM guidelines to create transfer datasets
  • Participating in project meetings (internal and external)

Develops and maintains clinical programming standard operating procedures by:

  • Participating in the development of data editing conventions, specification documents and Clinical Data
    Management (CDM) processes
  • Contributing to, designing and maintaining a library of reusable code
  • Leading and managing enhancements to current CDM systems and providing inputs in the implementation of
    new systems.

Ensures project timelines are maintained by:

  • Working independently and efficiently with minimal input required from the manager. Reviewing timelines;
    and projecting estimates and target dates in conjunction with direct supervisor and project team
  • Adhering to target dates for project timelines
  • Communicating any changes in target date to appropriate personnel including Project Manager
  • Keeping department head informed of progress as well as potential impediments

Maintains Quality Service and Departmental Standards by:

  • Adhering to established processes and standards
  • Reading, understanding and adhering to organizational Standard Operating Procedures (SOP)
  • Assisting in establishing and enforcing departmental standards
  • Maintain and review clinical programming SOPs
  • Participating in the modification of company SOPs

Maintains Quality Service and Departmental Standards by

  • Reading, understanding and adhering to organizational Standard Operating Procedures (“SOP”)
  • Assisting in establishing and enforcing departmental standards

Contributes to team effort by

  • Working with internal staff to resolve issues
  • Exploring new opportunities to add value to organization and departmental processes
  • Helping others to achieve results
  • Performing other duties as assigned

Maintains Technical and Industry Knowledge by

  • Attending and participating in applicable company-sponsored training

SECONDARY RESPONSIBILITIES

Contributes to team effort by:

  • Working with internal staff to resolve issues
  • Exploring new opportunities to add value to organization and departmental processes
  • Helping others to achieve results
  • Performing other duties as assigned

QUALIFICATIONS

Education:

  • Bachelor’s or Master’s degree in computer science, life sciences or related field required
  • SAS Certified Professional considered a plus
    Experience:
  • 3 years SAS programming experience in pharmaceutical related industry required (1 year with Master’s
    degree)
  • Experience working with CDISC, SQL, and Relational Databases preferred
  • Demonstrated programming skills required
  • Working knowledge and solid understanding of database organization and how to extract data in order to
    generate listings and reports
  • Proven ability in analyzing data
  • Understanding of medical and/or clinical trial terminology is desirable
  • Proven ability in problem solving

Additional Skills:

  • Ability to work in group setting and independently; ability to adjust to changing priorities
  • Excellent attention to detail and orientation toward meticulous work
  • Strong interpersonal and communication skills, both verbal and written
  • Strong documentation and organizational skills
  • Ability to project and maintain a professional and positive attitude
  • Excellent English

Please send your CV to hr@4createsoft.com

Objavljen od 04 Jun Pogledano 435 puta
Objavljen od 04 Jun Pogledano 435 puta
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