Find Associate director environment Jobs in Sutton, D

Clinical Quality Assurance - Program Lead (Associate Director)
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- Part-time
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Cushman & Wakefield —DUBLIN 2, County Dublin
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Trinity Access Programmes Internship Role x 4
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Novartis —Dublin, County Dublin
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ICON Plc —Dublin, County Dublin
- Full-time
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Join AECOM's growing Transportation Team in Ireland
AECOM —Dublin, County Dublin
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Jacobs —Dublin, County Dublin
- Hybrid work
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Associate Director - Finance
Turner & Townsend —Dublin, County Dublin
- Full-time
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Ethos —Dublin, County Dublin
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Account Management, Associate Director - Healthcare Data & Technology
IQVIA —Dublin, County Dublin
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Associate Director, Dispute Advisory
Interpath Advisory —Dublin, County Dublin
- Hybrid work
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Senior Associate, Customer Supply Chain
West Pharmaceutical Services —Dublin, County Dublin
- €63,300–€80,600 a year
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Clinical Quality Assurance - Program Lead (Associate Director)

Novartis -
Dublin, County Dublin

Apply Now

Job details

Full-time
€72,800–€135,200 a year

Qualifications

Doctoral degree
Google Cloud Platform
Master's degree
Bachelor's degree
Product development

Full job description

Summary

Employment Type: Full‑time | Regular, Hybrid, #LI-hybrid
Location: London (The Westworks) or Dublin (NOCC)

Novartis is unable to offer relocation support for this role: please only apply if the locations of Westworks, London or Dublin are accessible for you

The Associate Director, Clinical Quality Assurance (QA) will provide Quality oversight for the end-to-end clinical process for the clinical trials under responsibility to ensure compliance with the Health Authorities requirements, the internal standards and a full adherence to patients’ safety, rights and well-being.

About the Role

Major Accountabilities:

Proactively provide QA leadership to the business strategy for assigned programs/trials by ensuring considerable organization awareness (e.g. Interrelationship of departments and business priorities),
Drive implementation of quality strategy within Global Clinical Team (GCT )/ Clinical Trial Team (CTT) under responsibility
Regularly monitor the implementation of the annual Quality Plan pertaining to the assigned programs/studies
Ensure adequate oversight of proactive quality risk management process in the overseen areas including quality risk assessments and submission/inspection readiness activities and ensure that Clinical Trial Process (CTP) are in control
Provide robust and clear quality oversight in the following areas of clinical development: Support/collaborate with key stakeholders (e.g., Country Development Quality (CDQ), Development Units (DUs), GCT and/or CTT members) to ensure that risks are detected and remediated.Support core governance for quality incident management for critical and major deviations pertinent to the programs being assigned and ensure timely escalation when required.Provide Good Clinical Practice (GCP) guidance to day-to-day questions arising from Clinical trials deliverables.Collaborate with Country Development QA and External Service Providers (ESP) QA to drive initiatives relevant to internal monitoring and outsourced activities Quality oversight.Lead inspections preparation and facilitation in collaboration with other QA groups within Research & Development Quality (RDQ).Support audits and inspections follow-up activities including Corrective & preventative Actions (CAPA) preparation.
Actively leverage audit/inspection outcomes/trends to sustain improvement in clinical trials conduct.
Active participation in continuous improvement initiatives (including Work streams) and ensure that areas identified as weaknesses are properly being addressed and executed for sustainability
Be QA point of contact for the defined trials and attend the meetings and ensure quality is embedded in the decision taking processes.

Essential Requirements:

Bachelor’s degree in life science or healthcare field required. Advanced degree or equivalent education/degree in life sciences/healthcare preferred (PhD/MD/ PharmD/ Masters).
Extensive experience of involvement in regulated activities (GCP/ Pharmacovigilance (PV)), clinical development and/or QA positions with strong understanding on clinical trials
Broad understanding of global expectations of Health Authorities in the area of Clinical Development and profound understanding of the science of product development.
Ability to work independently and in a global/matrix environment.
Experience in managing projects.
Strong skills in GCP, quality and/or clinical development

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)

Primary location salary range

€72,800.00 - €135,200.00

Division

Development

Business Unit

Quality

Location

Ireland

Site

Dublin (NOCC)

Company / Legal Entity

IE02 (FCRS = IE002) Novartis Ireland Ltd

Functional Area

Quality

Job Type

Full time

Employment Type

Regular

Shift Work

Apply Now

Refine Your Search

associate director environment jobs in sutton, d

Clinical Quality Assurance - Program Lead (Associate Director)

Associate Director, Pharmacology

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Associate Director

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