20 publicaciones de empleo destacadas de clinical research en alcobendas, md (¡Están contratando!)

Associate Medical Director- Neurology
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Associate Pharmacovigilance Project Manager (Europe)
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Project management
- Liderazgo
Solicitud rápida
Associate Director, Field Medical Execution - Neuroscience
Novartis —Madrid, Madrid provincia
- De 73.100 € a 135.700 € al año
- Jornada completa
- CRM software
- Doctorado
- Inglés
CRA I-II in Madrid. Sponsor dedicated.
サイネオス・ヘルス —Madrid, Madrid provincia
- Grado
8d
Senior Director, Drug Development
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Investigación
- Teletrabajo opcional
Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Senior Site Contract Associate - IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Microsoft Office
- Grado
- Teletrabajo opcional
Product Data Officer - Medical Devicer (Fixed-Term Contract)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
6d
Compliance - Senior Consultant (Life Science exp mandatory)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Grado
Sr Medical Project Manager
Gilead Sciences —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Inglés
8d
Senior Statistician
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Máster
Solicitud rápida
7d
Senior Director / Executive Director Medical Writing
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Liderazgo
Solicitud rápida
Artificial Intelligence Research Scientist
SpotLab —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Informática
Solicitud rápida
Core Information Offering Specialist - MedTech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Inglés
- Teletrabajo opcional
1d
Access Field Head
Novartis —Madrid, Madrid provincia
- De 109.800 € a 204.000 € al año
- Jornada completa
- Negociación
8d
Proposals Manager - Pharmacovigilance
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Investigación
Solicitud rápida
Account Manager
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Ventas
- Servicio al cliente
- Grado
- Teletrabajo opcional
Senior Medical Information Associate Italian Language
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Servicio al cliente
- Inglés
- Habilidades de comunicación
Solicitud rápida
Senior Pharmacovigilance Officer, Team Lead/ Case Processing Manager- Medical Device experience needed
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Inglés
- Microsoft Office
- Gestión del tiempo
Solicitud rápida
Talent Acquisition Specialist EMEA
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Servicio al cliente
- Inglés
6d

Quiero recibir la alerta de empleo más reciente de clinical research en alcobendas, md

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Associate Medical Director- Neurology

IQVIA -
Madrid, Madrid provincia

Solicitar ahora

Detalles del empleo

Jornada completa

Beneficios

Teletrabajo opcional

Cualificaciones

Inglés
Desarrollo de negocios

Descripción completa del empleo

Madrid, Spain | Full time | Home-based | R1550098

Job Overview

The Associate Medical Director / Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a medical expert during project delivery lifecycle. Provide therapeutic and medical expertise to business development activities.

Essential Functions

The role includes predominantly Medical Monitoring responsibilities with Medical Strategic input involvement as requested.

Medical Monitoring:

Primarily serves as Global and /or Regional Medical Advisor on assigned projects.
Serves as Scientific Advisor and provides guidance to Project Leaders on the medical and scientific aspects of assigned projects.
Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.
Performs medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs).
Provides therapeutic area/indication training for the project clinical team.
Attends and presents at Investigator Meetings.
Performs review and clarification of trial-related Adverse Events (AEs).
May perform medical case review of Serious Adverse Events (SAEs), including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department.
May provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department.
May perform medical review of adverse event coding.
Performs review of the Clinical Study Report (CSR) and patient narratives.
Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.
Available 24/7 to respond urgent protocol -related questions from investigative sites, in accordance with local labor laws.

Medical Strategy:

Provides expert advises to the development of medically sounded delivery strategies for small to large and/or complex multi-region studies in partnership with sales and other functions responsible for business development activities.
Responsible for the development of the medically related aspects of client proposals including the budget related to medical monitoring.
Provides medical and scientific advises to key internal stakeholders developing proposals: this may include, but is not limited to, reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.
Attends and presents at bid defense meeting, as required.
Participates in strategic business development activities including presentations to prospective clients.
Maintains awareness of industry development and may author related publications.
Requires periodic regional and international travel.

Qualifications

Medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education, plus a minimum of 5 years' experience in clinical medicine.
Specialty board certification- Neurology
Ideally, candidate will have a minimum 2 years clinical trials experience as an investigator or medical /clinical expert in the Pharma, CRO, or Biotech industry.
Ability to establish and maintain effective working relationships with co-workers, managers and clients.
Strong communication, presentation and interpersonal skills, including good command of English language (both written and spoken).
Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in applicable therapeutic area.
Proven skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility.

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

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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clinical research empleos en alcobendas, md

Associate Medical Director- Neurology

Associate Pharmacovigilance Project Manager (Europe)

Associate Director, Field Medical Execution - Neuroscience

CRA I-II in Madrid. Sponsor dedicated.

Senior Director, Drug Development

Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience

Senior Site Contract Associate - IQVIA Biotech

Product Data Officer - Medical Devicer (Fixed-Term Contract)

Compliance - Senior Consultant (Life Science exp mandatory)

Sr Medical Project Manager

Senior Statistician

Senior Director / Executive Director Medical Writing

Artificial Intelligence Research Scientist

Core Information Offering Specialist - MedTech

Access Field Head

Proposals Manager - Pharmacovigilance

Account Manager

Senior Medical Information Associate Italian Language

Senior Pharmacovigilance Officer, Team Lead/ Case Processing Manager- Medical Device experience needed

Talent Acquisition Specialist EMEA

Quiero recibir la alerta de empleo más reciente de clinical research en alcobendas, md

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