Find clinical data manager Jobs in dublin county dublin

QA Manager & Qualified Person (QP)
RxSource —Dublin, County Dublin
- Engineering
- Bachelor's degree
- No degree
Technical Product Manager
Optum —Dublin, County Dublin
- Full-time
- Computer Science
- Bachelor's degree
- Agile
Area Director
IVC —Dublin, County Dublin
- Remote
- Mentoring
- Leadership
Health and Social Care Transformation Senior Manager, Hybrid
Deloitte —Dublin, County Dublin
- Full-time
- Hybrid work
- Business
Sr. Manager, Medical Writing
Alfasigma Group —Dublin, County Dublin
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
14d
Research Assistant (Research Nurse Manager)
Trinity College Dublin —Dublin, County Dublin
- Full-time
8d
Clinical Supply Specialist
ICON Plc —Dublin, County Dublin
- Full-time
- Microsoft Word
- Microsoft Excel
- Bachelor's degree
- Annual leave
- Employee assistance program
Data Migration Specialist
Lanas Healthcare Technology Ltd —DUBLIN 24, County Dublin
- Computer Science
- SQL
- Analysis skills
- Annual leave
- Employee assistance program
Quick apply
6d
Senior Manager - Finance Transformation - 12 month Contract
ICON Plc —Dublin, County Dublin
- Full-time
- No degree
- Annual leave
- Employee assistance program
Health & Social Care Transformation Director, Hybrid
Deloitte —Dublin, County Dublin
- Full-time
- Hybrid work
- Business
Principal Clinical Data Scientist
Novartis —Dublin, County Dublin
- Full-time
- Master's degree
- Organisational skills
- Agile
Business & Operations Manager Surgical Directorate
Beaumont Hospital —Dublin, County Dublin
- €83,911–€101,207 a year
- Full-time
- Management
- Master's degree
- Analysis skills
5d
Clinical Engagement Project Manager
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Hotel
- Project management
- Presentation skills
- Gym membership
- Life insurance
Quick apply
Senior Clinical Data Analyst
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Microsoft Excel
- Data analysis skills
- Master's degree
- Gym membership
- Life insurance
Quick apply
Internal Account Director (Recruitment & Retention)
サイネオス・ヘルス —Dublin, County Dublin
- €97,300–€170,300 a year
- Remote
- Microsoft Office
- Leadership
Lead Technical Product Manager
Optum —Dublin, County Dublin
- Full-time
- No degree
- Product management
- Agile
14d
Associate Director, Pharma Account Manager
Optum —Dublin, County Dublin
- Full-time
- Management
- Master's degree
- No degree
Radiographer - FTC
Beacon Hospital —Dublin, County Dublin
- Full-time
- Maths
- Bachelor's degree
Quick apply
13d
Health & Social Care Transformation Senior Consultant, Hybrid
Deloitte —Dublin, County Dublin
- Full-time
- Hybrid work
Territory Manager (Ireland North)
Cordis —DUBLIN 1, County Dublin
- Full-time
- Remote
- Sales
- Presentation skills
- Bachelor's degree

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QA Manager & Qualified Person (QP)

RxSource
Dublin, County Dublin

Apply Now

Job details

Qualifications

Engineering
Bachelor's degree
Packaging
Quality systems
Manufacturing

Full job description

At RxSource, our culture of appreciation and hard work fuels our success in improving patient's lives.
Join us and be recognized for your contributions to our purpose-driven movement.

Why Work for RxSource?

Our Culture

We have a supportive and welcoming culture that believes in giving back. We offer a paid days leave for volunteering to improve the lives of patients.

Fun-Filled Workplace

With team-building events and your birthday day off, we aim to provide a dynamic and enjoyable work experience for all employees. Join us and discover a fresh perspective on work.

Own-it

With our "Own It" mentality, we encourage responsibility, continuous learning, and growth. And to help you on your journey, we offer reimbursement for courses and training for professional development.

QA Manager & Qualified Person (QP)
Dublin, Ireland

Description

Position Summary:

The QA Manager & Qualified Person (QP) is the senior Quality representative at the Dubin, Ireland facility and is responsible for the effective implementation, maintenance, and continuous improvement of the site Pharmaceutical Quality System (PQS) locally. This role provides quality oversight of GMP/GDP operations supporting packaging, labeling, QP certification, and distribution of investigational medicinal products (IMPs) in support of clinical trials.

In addition, this role performs Qualified Person (QP) duties in accordance with EU GMP, Annex 13, Annex 16, the Manufacturing/Importation Authorization (MIA), and applicable EU and national legislation, certifying IMP batches for release for clinical trial use.

The role serves as the primary site Quality lead, supporting inspections, audits, supplier qualification, quality events management, and training, while partnering cross?functionally to embed a strong culture of quality and compliance. On?site Quality personnel will report to the QA Manager & Qualified Person (QP).

Responsibilities:

QA Manager Responsibilities:

Ensure ongoing compliance with EU GMP, GDP, HPRA expectations, and internal SOPs.
Maintain and continuously improve the site Pharmaceutical Quality System (PQS).
Act as Quality lead for the Dubin facility, providing daily QA oversight of operations.
Review and approve controlled documents such as SOPs and work instructions.
Provide QA oversight for clinical trial related services, including receipt, storage, label printing, secondary packaging and labeling, and distribution of products used in clinical trials.
Review and approve clinical packaging and labeling batch documentation.
Provide QA oversight of activities such as temperature monitoring, sanitation, environmental controls, calibration, and preventive maintenance.
Ensure GMP/GDP facilities, systems, and equipment maintain a qualified/validated state.
Review, approve, and manage deviations, CAPAs, change controls, risk assessments, complaints, and investigations within the EQMS ensuring data integrity and timely closure.
Lead or support root cause investigations and ensure timely, effective corrective and preventive actions.
Support and execute product recalls in accordance with SOPs and legal/regulatory guidance when required.
Host and support customer audits, regulatory inspections, and internal self?inspections.
Ensure inspection readiness and timely, compliant responses to audit observations.
Serve as a Quality point of contact for customers and regulatory authorities as needed.
Qualify, assess, and monitor suppliers and service providers using a risk-based approach.
Review and maintain Quality Agreements / Technical Agreements with suppliers and customers.
Develop, deliver, and oversee GMP/GDP and SOP training programs and assess training effectiveness.
Assess training effectiveness and identify ongoing training needs.
Assist in recruiting, onboarding, coaching, and mentoring Quality team members.
Promote a proactive quality culture across all functions and levels.
Drive continuous improvement initiatives to enhance compliance, efficiency, and quality performance.
Track, trend, and report quality metrics to senior management and support management review activities.
Stay current with changes in US and global pharmaceutical regulations, guidance, and industry best practices.

Qualified Person Responsibilities:

Act as a named Qualified Person on the site MIA and perform QP duties as defined in site SOPs and Quality Agreements.
Certify and release IMP batches in accordance with EU GMP, Annex 13, Annex 16, CTA/IMPD requirements, and national legislation.
Ensure that all manufacturing, testing, packaging, and supply chain activities comply with EU GMP and the approved clinical trial authorization.
Verify that manufacturing and testing sites are appropriately authorized and GMP compliant.
Confirm completeness and compliance of batch documentation, investigations, validations, and QC data prior to certification.
Ensure appropriate qualification of starting materials, packaging materials, and suppliers.
Maintain appropriate oversight of any delegated QP?related activities, retaining full accountability for certification decisions.
Maintain up?to?date QP training and ensure ongoing regulatory and product knowledge.

Qualifications:

Required:
Bachelor’s degree in Pharmacy, Life Sciences Engineering, or a related discipline.
Educational qualifications meeting EU QP eligibility requirements as defined in Directives 2001/83/EC and applicable national legislation.
5+ years of Quality experience in pharmaceutical manufacturing, clinical trial packaging and labeling, pharmaceutical distribution within a GxP environment.
Strong working knowledge of EU GMP, Annex 13, Annex 16, GDP, and HPRA expectations.
Experience managing quality systems, audits, deviations, CAPAs, and change control.
Proven ability to work cross?functionally and manage multiple priorities.

Preferred:

Prior experience in a clinical trial supply services organization.
Experience serving as a named QP on an MIA IMP.
Experience leading or developing other Quality professionals.

Apply Now

Refine Your Search

clinical data manager jobs in dublin county dublin

QA Manager & Qualified Person (QP)

Technical Product Manager

Area Director

Health and Social Care Transformation Senior Manager, Hybrid

Sr. Manager, Medical Writing

Research Assistant (Research Nurse Manager)

Clinical Supply Specialist

Data Migration Specialist

Senior Manager - Finance Transformation - 12 month Contract

Health & Social Care Transformation Director, Hybrid

Principal Clinical Data Scientist

Business & Operations Manager Surgical Directorate

Clinical Engagement Project Manager

Senior Clinical Data Analyst

Internal Account Director (Recruitment & Retention)

Lead Technical Product Manager

Associate Director, Pharma Account Manager

Radiographer - FTC

Health & Social Care Transformation Senior Consultant, Hybrid

Territory Manager (Ireland North)

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At RxSource, our culture of appreciation and hard work fuels our success in improving patient's lives.
Join us and be recognized for your contributions to our purpose-driven movement.

Why Work for RxSource?

Our Culture

Fun-Filled Workplace

Own-it

QA Manager & Qualified Person (QP)
Dublin, Ireland

QA Manager & Qualified Person (QP)

Description

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clinical data manager jobs in dublin county dublin

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Explore jobs in more locations

At RxSource, our culture of appreciation and hard work fuels our success in improving patient's lives. Join us and be recognized for your contributions to our purpose-driven movement.

Why Work for RxSource?

Our Culture

Fun-Filled Workplace

Own-it

QA Manager & Qualified Person (QP)

Description

At RxSource, our culture of appreciation and hard work fuels our success in improving patient's lives.
Join us and be recognized for your contributions to our purpose-driven movement.