20 publicaciones de empleo destacadas de compliance pharmaceutical en madrid madrid provincia (¡Están contratando!)

Compliance - Senior Consultant (Life Science exp mandatory)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Grado
Medical Information Specialist - (French & English Speaking)
EVERSANA —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Microsoft Word
- Microsoft Excel
- Inglés
Solicitud rápida
8d
Accreditation & Compliance Coordinator
Kenes Group Ltd —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Microsoft Office
- Project management
Accreditation & Compliance Coordinator
Kenes Group —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Microsoft Office
- Project management
Global Medical Education Assistant
Silimed —Alcorcón, Madrid provincia
- Jornada completa
- Teletrabajo
- Español
- Inglés
- Experiencia administrativa
Solicitud rápida
Quality Assurance & Regulatory Affairs Specialist - Temporary position
Ferring Pharmaceuticals, Inc. —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Máster
Clinical Associate
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Grado
- Gestión del tiempo
- Seguro dental
- Seguro oftalmológico
4d
MSL Parkinson
AbbVie —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Doctorado
- Inglés
- Investigación
14d
Study Start Up Associate II
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Seguro dental
- Seguro oftalmológico
1d
Quality Control Associate, Bioassay
Moderna, Inc. —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Control de calidad
- Vacaciones pagadas
Customer Quotation Representative
Cencora —Madrid, Madrid provincia
- Jornada completa
- Microsoft Word
- CRM software
- Microsoft Excel
EVENT PROJECT MANAGER - DEDICATED PHARMA CLIENT TEAM (f/m/d)
egg —Madrid, Madrid provincia
- De 32.000 € a 35.000 € al año
- Teletrabajo
- Español
- Inglés
- Microsoft Office
- Abono gimnasio
Business Support Partner, Metabolic Diseases
Sobi —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Español
- Microsoft Excel
Solicitud rápida
7d
Clinical FSP Director Quality - Client Dedicated- Regional Clinical Compliance Inspection Lead
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Microsoft Office
- Teletrabajo opcional
8d
Office Manager - part-time: 4 days pw
osapiens —Madrid, Madrid provincia
- Microsoft Powerpoint
- Microsoft Word
- Español
Solicitud rápida
7d
Contracting and Tender Lead
Takeda Pharmaceutical —Madrid, Madrid provincia
- De 70.000 € a 96.250 € al año
- Jornada completa
- Hospital
- Inglés
- Máster
14d
Clinical FSP Quality Manager
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Microsoft Office
- Teletrabajo opcional
11d
Senior Consultant Product Compliance (m/f/x)
osapiens —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
Solicitud rápida
Senior Specialist, Quality Control, Chemistry
Moderna, Inc. —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Control de calidad
- Vacaciones pagadas
Global Trial Delivery Lead - Sponsor Dedicated
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
- Teletrabajo opcional

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Compliance - Senior Consultant (Life Science exp mandatory)

IQVIA -
Madrid, Madrid provincia

Solicitar ahora

Detalles del empleo

Jornada completa

Cualificaciones

Derecho
Inglés
Máster
Grado
Liderazgo

Descripción completa del empleo

Madrid, Spain | Full time | Hybrid | R1547045

Join us on our exciting journey!

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward.

Job Overview

The Compliance Senior Consultant will work primarily on teams led by Engagement Managers and Principals to meet goals and objectives as outlined in client contracts/agreements. Under supervision, the Compliance Senior Consultant will develop and present project plans and proposals, will have a largely client facing role and may be the day to day client contact on projects. They are expected to oversee deliverables, timelines, and ongoing project execution. They will responsible for quality review of all staff deliverables. Special projects and internal projects will also be assigned on an as needed basis by Engagement Managers and Principals. Projects cover a variety of subject matter topics including:

Compliance Consulting (Programmatic design and implementation, business needs and risk assessments, benchmarking, and industry best practices
Commercial Operations and Business Process Enhancement (HCP/O engagement process design, operations, process transformation and support of technology rollouts)
Fair Market Value (FMV and HCP Tiering Methodology, Rate Analysis, FMV process implementation)
Transparency and Aggregate Spend (international laws and regulations such as US Sunshine Act, France Transparency and Engagement Notifications Requirements, EFPIA etc.)
Auditing and Monitoring (live monitoring, transactional and data analysis, compliance auditing)
Special projects and internal projects will also be assigned on an as needed basis

Responsibilities

Support and lead consulting projects
Lead clients in business workshops and interviews
Develops project deliverables which could include data analyses and reports, process reviews and assessments, policies, and SOPs etc.
Develop, articulate, and present ideas and opinions
Manage and take accountability for projects
Provide mentorship for junior staff members
Develop relationships with clients and identify future opportunities
Create project deliverables with some oversight by senior staff
Support in growing the organization
Other duties as assigned

Skills & Experience

Client Relationship Delivery – Day-to-day owner of client delivery within leading Life Sciences organizations, focused on client satisfaction and outstanding client deliverables.
Analytical Problem-Solving - Applies an analytical approach to solving problems and reaching logical conclusions. Gathers information from a variety of sources and quickly gains an understanding of it. Works effectively with complicated, conflicting, or ambiguous information, and looks beyond the surface of issues to identify their underlying patterns and causes.
Effective Communication - Expresses ideas in a clear and concise manner; tailors’ message to target audience and can communicate effectively both verbally as well as in writing

Qualifications & Other Requirements - our ideal candidate will have

Minimum 4 - 6 years strategic management consulting or legal experience, preferably with a Big 4, strategy consulting, specialized healthcare consulting or law firm
Undergraduate degree or equivalent experience required; MBA, a Law Degree (JD or other equivalent) or another master’s degree preferred
Successful track record delivering projects (on time and on budget)
Strong presentation and communication skills (written and verbal)
Entrepreneur, independent worker, organized, self-motivated
Analytical and quantitative: comfortable with numbers, strong business acumen, and excellent leadership skills
Willingness to have a different opinion, ability to articulate thoughts and concepts well
Ability and willingness to strive to improve skills related to the IQVIA core competencies
Willingness to travel
Experience or knowledge of pharmaceutical industry and in particular compliance and risk management issues a strong plus

PLEASE SUBMIT YOUR CV IN ENGLISH! THIS ROLEIS NOT OPEN TO VISA SPONSORSHIP.

Join us on our exciting journey!

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.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Where you'll work

Hybrid

You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.

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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compliance pharmaceutical empleos en madrid madrid provincia

Compliance - Senior Consultant (Life Science exp mandatory)

Medical Information Specialist - (French & English Speaking)

Accreditation & Compliance Coordinator

Accreditation & Compliance Coordinator

Global Medical Education Assistant

Quality Assurance & Regulatory Affairs Specialist - Temporary position

Clinical Associate

MSL Parkinson

Study Start Up Associate II

Quality Control Associate, Bioassay

Customer Quotation Representative

EVENT PROJECT MANAGER - DEDICATED PHARMA CLIENT TEAM (f/m/d)

Business Support Partner, Metabolic Diseases

Clinical FSP Director Quality - Client Dedicated- Regional Clinical Compliance Inspection Lead

Office Manager - part-time: 4 days pw

Contracting and Tender Lead

Clinical FSP Quality Manager

Senior Consultant Product Compliance (m/f/x)

Senior Specialist, Quality Control, Chemistry

Global Trial Delivery Lead - Sponsor Dedicated

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Qualifications & Other Requirements - our ideal candidate will have

Where you'll work

Hybrid

Culture

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