20 publicaciones de empleo destacadas de clinical project en madrid, md (¡Están contratando!)

Clinical FSP Quality Manager
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Microsoft Office
- Teletrabajo opcional
12d
Study Start Up Associate II
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Seguro dental
- Seguro oftalmológico
2d
Senior Clinical Trial Manager - Internal Medicine
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Grado
- Liderazgo
- Seguro dental
- Seguro oftalmológico
9d
Global Clinical Trial Manager
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Liderazgo
- Seguro dental
- Seguro oftalmológico
8d
Medical Engagement Partner Cardiometabolic Diseases - Noreste y Norte
Roche —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
7d
EMEA Strategy Consultant - Wolters Kluwer Health
Wolters Kluwer —Salamanca-Madrid, Madrid provincia
- Horas extra
- Microsoft Powerpoint
- Microsoft Word
- CRM software
Clinical Trial Manager - IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Project management
- Grado
- Teletrabajo opcional
Senior Site Contract Associate - IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Microsoft Office
- Grado
- Teletrabajo opcional
Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Doctorado
- Investigación
- Máster
Compliance - Senior Consultant (Life Science exp mandatory)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Grado
Clinical Trials Vendor Management Specialist
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Microsoft Office
- Desarrollo de negocios
Solicitud rápida
Medical Scientist Lead
Gilead Sciences —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Inglés
Global Trial Delivery Lead - Sponsor Dedicated
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
- Teletrabajo opcional
Legal Counsel EMEA M&A
IQVIA —Madrid, Madrid provincia
- De 180.300 € a 383.100 € al año
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
Training & Education Specialist, Urology - EMEA (Sacral Neuromodulation)
Boston Scientific —Madrid, Madrid provincia
- Trabajo híbrido
- Inglés
- Project management
- Marketing
Diagnostic Liason - Galicia y Castilla y León
AstraZeneca —Madrid, Madrid provincia
- Jornada completa
- Microsoft Excel
- Doctorado
- Ventas
8d
Patient Safety & Medical Affairs Delivery Manager
Roche —Madrid, Madrid provincia
- Jornada completa
- Agile
- Liderazgo
- Negociación
Business Account Specialist - Cantabria, País Vasco, Palencia y León
AstraZeneca —Madrid, Madrid provincia
- Jornada completa
- Microsoft Excel
- Inglés
- Grado
Iberian Country Marketer (m/f/x)*
Solventum —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Español
- Microsoft Excel
12d
Healthcare Panel Specialist French / German
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Excel
- Servicio al cliente
- Inglés
12d

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Clinical FSP Quality Manager

IQVIA -
Madrid, Madrid provincia

Solicitar ahora

Detalles del empleo

Jornada completa
Hace 12 días

Beneficios

Teletrabajo opcional

Cualificaciones

Investigación clínica
Inglés
Investigación
Microsoft Office
Grado
Negociación

Descripción completa del empleo

Madrid, Spain | Full time | Home-based | R1558535

Job Description Summary

This role is an individual contributor assigned to designated Delivery Unit(s), sponsor(s), business line(s), and/or specific tasks as defined by the line manager (LM). The purpose of this role is to work together with global or regional Quality Management team(s), functional teams, and other stakeholders in a joint effort to clearly define the global Quality Plan, carry out, and adopt the plan according to the specific needs defined by the scope of assignment, assist staff in improving compliance with relevant International Conference on Harmonization (ICH), Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), Key Performance Indicators (KPIs), applicable regulatory requirements, and guidelines.
This role provides advice and supports clinical staff and other relevant key stakeholders with regard to quality control, risk management, and corrective/preventive actions.

Essential Functions

Conduct country and site-level compliance oversight using a risk-based approach.
Identify compliance risks, conduct site assessments, and manage CAPAs.
Support inspections and audits while serving as the local GCP expert.
Drive inspection readiness and compliance at the country level.

Adopt and implement the global Quality Management Plan within the scope of the assignment, this will include: Planning and executing the Quality Management activities. Risk identification and assessment through data review and quality control processes. Providing support in risk mitigation, in planning corrective/preventive actions, and guidance for improvement. Supporting the assigned business line management and staff to enhance effectiveness.;
Cooperate closely with the relevant business and other stakeholders, support maintaining focus on quality in project delivery.
Contribute to the development and implementation of a Delivery Unit/Sponsor specific Quality Management plan and Risk Management Program, monitor the implementation and delivery.
Provide advice and support to teams within the assigned business line and other key stakeholders on all aspects of Good Clinical Practice (GCP) compliance.
Work in close cooperation with teams to manage non-compliance, quality issues, support in planning corrective/preventive actions, as applicable according to Standard Operating Procedures (SOPs.);

Inform Quality Management, the assigned business line, and Quality Assurance of quality issues according to SOPs.;

Inform Quality Management, the assigned business line, and Quality Assurance of quality issues according to SOPs.
Work closely with Quality Assurance and assigned business staff in case of suspected misconduct, as required by the applicable SOPs.
May provide assistance during audits and regulatory inspections to the teams to the extent agreed with the business lines, as required by the applicable SOPs.
Act as the primary contact for Quality Assurance on quality matters – on the level of the assignment, attend meetings/teleconferences.
Prepare periodic reports to business lines on quality related matters, risk assessments and specific quality improvement initiatives.
Upon agreement with the line manager: Perform any other reasonable tasks as required by the role.

Qualifications

9+ years total experience.
Clinical Operations background plus GCP/compliance experience.
Strong site oversight and risk management experience.
Oncology experience preferred.
Bachelor's Degree Bachelor's Degree or equivalent qualification Req
Equivalent combination of education, training, and experience.
Sound working knowledge of medical terminology, Standard Operating Procedures (SOPs), International Conference on Harmonization (ICH), Good Clinical Practice (GCP), applicable regulatory requirements, quality management processes.
Knowledge of National and International Regulations and Drug Development processes.
Knowledge of Clinical Research Organization (CRO) or Pharmaceutical industry operations.
Knowledge of IQVIA corporate standards and SOPs.
Good organizational, interpersonal and communication skills.
Good judgement and decision-making skills.
Strong influencing and negotiation skills.
Strong computer skills including Microsoft Office applications.
Excellent problem solving skills.
Ability to travel within the region/country.
Ability to lead and motivate a clinical team.
Ability to establish and maintain effective working relationships with co-workers, managers and clients/customers.
Fluent in English.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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Refina tu búsqueda

clinical project empleos en madrid, md

Clinical FSP Quality Manager

Study Start Up Associate II

Senior Clinical Trial Manager - Internal Medicine

Global Clinical Trial Manager

Medical Engagement Partner Cardiometabolic Diseases - Noreste y Norte

EMEA Strategy Consultant - Wolters Kluwer Health

Clinical Trial Manager - IQVIA Biotech

Senior Site Contract Associate - IQVIA Biotech

Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting

Compliance - Senior Consultant (Life Science exp mandatory)

Clinical Trials Vendor Management Specialist

Medical Scientist Lead

Global Trial Delivery Lead - Sponsor Dedicated

Legal Counsel EMEA M&A

Training & Education Specialist, Urology - EMEA (Sacral Neuromodulation)

Diagnostic Liason - Galicia y Castilla y León

Patient Safety & Medical Affairs Delivery Manager

Business Account Specialist - Cantabria, País Vasco, Palencia y León

Iberian Country Marketer (m/f/x)*

Healthcare Panel Specialist French / German

Quiero recibir la alerta de empleo más reciente de clinical project en madrid, md

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