Associate Director

3 weeks ago


Remote, United Kingdom Ark Talent Group Full time

Title: Associate Director - ICSR (Global Patient Safety Operations)

Location: Remote

Contract Length: 12 months

IR35 Status: Outside (LTD)

Our client is looking for an **Associate Director** to join the **Global PS Operations, Technology & Analytics group in Patient Safety, CMO.**

The team is responsible for the management of assigned projects, processes and partnerships including implementation, communication, compliance, performance, vendor oversight and inspection readiness within the ICSR area.

Key responsibilities will include:

- Identify opportunities for and drives the enhancement of existing processes and partnerships through knowledge of internal and external environment
- Working with the PV Process, Partnership and Patient Safety and Regulatory experts, develop, establish, monitor, report and assess global KPIs related to safety and regulatory data reporting
- Utilise safety and regulatory knowledge to maintain and support the global inspection readiness strategy
- Manages relationships/partnerships/alliancesexternal to the AZ CMO function that are essential to delivering AstraZeneca’s pharmacovigilance and regulatory LTO responsibilities
- Identify opportunities for and drives the enhancement of existing processes and partnerships through knowledge of internal and external environment
- Working with the PV Process, Partnership and Patient Safety and Regulatory experts, develop, establish, monitor, report and assess global KPIs related to safety and regulatory data reporting.
- Utilise safety and regulatory knowledge to maintain and support the global inspection readiness strategy.
- Manages relationships/partnerships/alliancesexternal to the AZ CMO function that are essential to delivering AstraZeneca’s pharmacovigilance and regulatory LTO responsibilities
- Provide support and oversight to the outsourcing partner(s) to facilitate compliance with regulatory and legal requirements and maintaining inspection

You will also have:

- Experience in working cross-functionally
- Leadership skills, including proven leadership of project teams experience
- Thorough scientific knowledge sufficient to understand all aspects of regulatory/pharmacovigilanceand partnership issues
- Thorough knowledge of the drug development process

**Job Types**: Temporary contract, Fixed term contract, Freelance
Contract length: 12 months

**Salary**: £550.00-£614.00 per day

**Benefits**:

- Work from home

Schedule:

- Monday to Friday

**Education**:

- Bachelor's (preferred)

**Experience**:

- Pharmaceutical: 5 years (preferred)
- pharmacovogilance: 5 years (preferred)
- Regulatory: 5 years (preferred)
- Patient Safety: 5 years (preferred)

Work Location: Remote



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