Ethics Risk

2 weeks ago


Riyadh, Ar Riyāḑ, Saudi Arabia Novartis Full time

Position Purpose:

  • Support the implementation and continuous improvement of an effective Compliance program with specific focus on relevant health regulations (e.g., fraud & abuse, promotional/nonpromotional, clinical) and industry codes. Lead the development and execution of effective monitoring and remediation activities in assigned country/ region.


Major Accountabilities
  • In collaboration with the ERC Head, Regional ERC Team and other key stakeholders, support the development and implementation of the Cluster ERC monitoring program.
  • Support in assessing and monitoring ERC policy/risk areas based on applicable regulations, codes and country/region risk profile; creates thorough analytic reviews and management reports.
  • Analyse the quality of the data and processes in place and liaise with the ERC head to ensure the performance of timely, sound and factbased Risk Assessments, Self-Assessments and related monitoring activities.
  • Communicate deviations to the business; develop appropriate remediation plans, and followup with countries to ensure adequate implementation of those actions.
  • Identify areas of improvement in countries' systems and/or processes to increase efficiency and strengthen effectiveness.
  • Foster an advisory, proactive and collaborative approach regarding Compliance.
  • Support as required investigations of alleged misconduct based on allocation of responsibility by the SpeakUp Team.

Commitment to Diversity & Inclusion:

  • Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve._

Minimum requirements

  • Education: University degree in Science or Business Marketing plus further postgraduate qualification or MBA.
  • Languages: English & Arabic.
  • Experience/Professional Requirements:
  • Minimum 1-2 years of experience in finance, compliance or an internal audit function, in the pharmaceutical, device or healthcare industries, with a baseline under-standing of Country and Regional legislation and guidelines (eg., FCPA, UK Bribery Act, EFPIA, EGA); Audit/monitoring in the clinical research area is a plus.
  • Experience in a highly regulated industry with its dynamics, regulatory framework.
  • Ability to lead complex projects and collaborate within and across crossfunctional teams and business units, in a matrixes environment
  • Crisis management.

Division

  • PHARMA

Business Unit

  • AMAC

Country

  • Saudi Arabia

Work Location

  • Riyadh

Company/Legal Entity

  • SAUDI PHARMA DISTRIB SAU

Functional Area

  • Legal & Intellectual Property & Compliance

Job Type

  • Full Time

Employment Type

  • Regular

Shift Work

  • No

Early Talent

  • Yes


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