20 publicaciones de empleo destacadas de director of compliance en madrid, md (¡Están contratando!)

Global Study Manager - Single Sponsor dedicated (in EMEA)
IQVIA —Madrid, Madrid provincia
- De 171.500 € a 404.600 € al año
- Jornada completa
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- Teletrabajo opcional
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Axepta —Madrid, Madrid provincia
- Español
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Senior Partner Finance Executive
Expedia —Madrid, Madrid provincia
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IQVIA —Madrid, Madrid provincia
- Jornada completa
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Unit4 —Madrid, Madrid provincia
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UST —Madrid, Madrid provincia
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Nordex SE —Madrid, Madrid provincia
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MANAGING DIRECTOR – GLOBAL HEAD OF ORIGINATION, WHOLESALE BANKING CASH MANAGEMENT
SCH Banco Santander, S.A. —Boadilla del Monte, Madrid provincia
- Jornada completa
- Español
- Inglés
- Abono gimnasio
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HR Administrative support ( Temporary)
MSX International —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Microsoft Powerpoint
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Head of Finance
Egis Group —Madrid, Madrid provincia
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Business Applications Lead
Destinus —Madrid, Madrid provincia
- 102.500 € al año
- Jornada completa
- Trabajo híbrido
- Informática
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- Inglés
Solicitud rápida
9d
Director - Health, Safety & Environment
J.S. Held LLC —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
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Aviation Senior Project Director
AECOM —Madrid, Madrid provincia
- Jornada completa
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Compensation & Benefits Specialist
Henry Schein España S.L. —Madrid, Madrid provincia
- 35.000 € al año
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Service Development Director - Anti Fraud
SGS —Madrid, Madrid provincia
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Commercial Director Energy Based Devices - Southern Europe
Sinclair —San Fernando de Henares, Madrid provincia
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Senior Medical Writer - FSP
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Word
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- Teletrabajo opcional

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Global Study Manager - Single Sponsor dedicated (in EMEA)

IQVIA -
Madrid, Madrid provincia

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Detalles del empleo

Jornada completa
De 171.500 € a 404.600 € al año

Beneficios

Teletrabajo opcional

Cualificaciones

Investigación clínica
Inglés
Investigación
Máster
Project management
Grado
Liderazgo

Descripción completa del empleo

Madrid, Spain | Full time | Home-based | R1534243

Job Overview

The Global Study Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clincal Operations, Study Management to time, cost and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study archiving.
The GSM works cross-functionally with internal and external partners to deliver delegated aspects of the clinical study in accordance with Global Study Director (GSD) or Global Study Associate Director (GSAD) in delegated aspects of clinical study execution in accordance with the Delivery Model.

Essential Functions

In partnership with client's team,

Leads/contributes to the preparation of delegated study documents (e.g., Informed Consent Form, master Clinical Study Agreement etc), and external service provider related documents (specifications, study specific procedures, descriptions, presentations etc.).
Maintains and facilitates interactions with internal functions and external functions including the CROs and other external service providers to ensure an efficient study delivery to time, costs and quality objectives.
Contributes to the planning and conduct of internal and external meetings (e.g., Investigators’/Monitors’ meeting).
Ensures the supply of Investigational product and study materials by liaising with Clinical Supply Chain or external service providers as appropriate.
Proactively contributes to risk and issue identification, development of mitigation and/or action plans for identified risks and issues.
Ensures that all study documents in scope of GSM’s responsibilities are complete and verified for quality in Trial Master File.
Supports GSD and/or GSAD with budget management, such as external service provider invoice reconciliation.
Adheres to global clinical processes, procedural documents, applicable Quality & Compliance manual documents and international guidelines such as ICH/GCP to ensure study is inspection ready at all times.
Supports GSD and/or GSAD with overall project management as per agreed delegation.
For outsourced studies, supports GSD and/or GSAD in management of the CRO Project Manager to ensure study delivery according to agreed timelines, budget and quality standards, while ensuring that the appropriate level of oversight of the CRO is maintained and documented throughout the lifecycle of the study, in accordance with

Internal BioPharmaceuticals Clinical Operations Job Description
relevant client's SOPs and guidelines (e.g., description of services and transfer of obligations)

Take on assignments on non-drug project work in process improvements and/or leading improvement projects as discussed and agreed upon with their manager

Qualifications

University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.
Relevant experience from within the pharmaceutical industry or similar organization or academic experience, preferably of at least 3 years.
Knowledge of clinical development / drug development process in various phases of development and therapy areas
Excellent knowledge of international guidelines ICH/GCP
Excellent communication and relationship building skills, including external service provider management skills
Good project management skills
Demonstrated ability to collaborate as well as work independently
Demonstrated leadership skills
Computer proficiency, advanced computer skills in day-to-day tasks
Excellent verbal and written communication in English

Please note this role is not eligible for the UK visa sponsorship.

Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered.

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.

The potential base pay range for this role, when annualized, is 171.500,00 zł - 404.600,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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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Quiero recibir la alerta de empleo más reciente de director of compliance en madrid, md

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