• Clinical Programmer Analyst II Jobs in Mysore,India - 23801284

  • BioClinica
  • Save Job
  • 1 - 3 Years
  • Posted : above 1 month

Job Description:

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


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


Maintains Technical and Industry Knowledge by


  • Attending and participating in applicable company-sponsored training


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 skill set
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
Working conditions
Travel 0-5%
Lifting 0-10lbs
Other Computer work for long periods of time
EEO Statement

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Profile Summary:

Employment Type : Full Time
Industry : FMCG / F&B
Salary : Not Disclosed
Deadline : 12th Apr 2020

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