Assoc Dir Statistical Programming

Year    Bangalore, Karnataka, India

Job Description


Who we are

Together, we\'re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It\'s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world\'s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization\'s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we\'re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

The clinical programming team provides programming support, develops and generates official outputs and datasets for regulatory purposes. The primary responsibility of the Associate Director is to provide professional expertise and leadership of all aspects related to clinical programming activities. The main responsibilities is to lead, mentor, educate and manage resources efficiently.

How you\'ll spend your day

  • Primarily works at the (multiple) product / program level
  • Provide input for Budget Planning
  • Possible to have direct reports; Oversee contingent workers and / or vendors; Provide training to others; Strategically analyze needs to manage resources
  • Manage and deliver assignments with quality and within timelines
  • Ensure that SOPs and guidelines are followed. Train programmers in SOPs, guidelines and in the proper use of the SAS system environment.
  • Leverage the team\'s professional standards and abilities, while preserving a fluent workflow with other interfacing departments.
  • Lead and manage the clinical programming team activities.
Your experience and qualifications

Bachelors/Masters/PhD in Science, Statistics, Information Technology or equivalent combination of education and related work experience.

Bachelor\'s + 9 years or Master\'s + 8 years or PhD + 3 years of professional experience in a pharmaceutical or clinical research setting as a programmer.

10 years of experience in SAS Programmer into SDTM &Adam\'s with TLG\'S (Table, Listing, Graphs)

Enjoy a more rewarding choice

Make a difference with Teva Pharmaceuticals

Already Working @TEVA?

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Teva\'s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva\'s global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

Teva Pharmaceuticals

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Job Detail

  • Job Id
    JD3132814
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Bangalore, Karnataka, India
  • Education
    Not mentioned
  • Experience
    Year