Clinical Quality Assurance - Program Lead

Novartis; London; Hybrid; GBP 80,000 - 100,000; Full time

Job summary

A leading pharmaceutical company in London is looking for an Associate Director in Clinical Quality Assurance. The role involves providing quality oversight for clinical trials ensuring compliance with regulations. Candidates should have extensive experience in quality assurance, strong leadership skills, and a background in life sciences. This position offers a hybrid working model and an opportunity to make a significant impact on patient safety.

Benefits

Collaborative environment

Comprehensive benefits package

Opportunities for professional development

Qualifications

• 7 years of involvement in regulated activities (GCP/Pharmacovigilance).
• Broad understanding of global expectations of Health Authorities.
• 3 or more years' experience in managing projects.

Responsibilities

• Provide QA leadership for assigned programs/trials.
• Monitor annual Quality Plan implementation for studies.
• Ensure quality risk management processes are in control.

Skills

Agility

Auditing

Leadership

Risk Management

Stakeholder Management

Education

Bachelor's degree in life science or healthcare

PhD/MD/PharmD/Masters

Job description

Overview

Job Description Summary
LOCATION: London, UK, Dublin, Rep of Ireland or Barcelona, Spain
ROLE TYPE: Hybrid Working, #LI-Hybrid

As an Associate Director level, Clinical Quality Assurance - Program Lead within Clinical Quality Assurance, you 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.

Responsibilities

• 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.
• Support 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).
• 7 years of involvement in regulated activities (GCP/ Pharmacovigilance (PV)), clinical development and/or QA positions.
• 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.
• 3 or more years' 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

Join our Novartis Network

Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

Benefits and Rewards

Read our handbook to learn about all the ways we'll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Skills Desired

Agility, Auditing, Audit Management, Business Partnering, Continued Learning, Drug Development, Employee Performance Evaluations, Health Authorities, Influencing Skills, ISO 9001, Leadership, Organizational Savvy, People Management, Qa (Quality Assurance), Quality Management, Quality Management Systems (QMS), Risk Management, Root Cause Analysis (RCA), Self-Awareness, Stakeholder Management, Technological Expertise, Vendor Management