Ethics Risk

1 week ago

Riyadh, 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/non-promotional, 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 re-views 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 fact-based Risk Assessments, Self-Assessments and related monitoring activities.
- Communicate deviations to the business; develop appropriate remediation plans, and follow-up 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 cross-functional 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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