20 publicaciones de empleo destacadas de associate director, alumni transition en spain (¡Están contratando!)

Associate Medical Director- Dermatology
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- Jornada completa
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Dedale Intelligence —Madrid, Madrid provincia
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FeverUp —Madrid, Madrid provincia
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SWE (Research team)
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FeverUp —Madrid, Madrid provincia
- Jornada completa
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Sr. Sales Associate
Coach —Pozuelo de Alarcón, Madrid provincia
- Disponibilidad fin de semana
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Director, Cost Management - Data Centres
Turner & Townsend —Madrid, Madrid provincia
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In-store Operations Manager
Fendi —Barcelona, Barcelona provincia
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Claims Delivery & Operations Manager
Chubb —Madrid, Madrid provincia
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Zurich Insurance —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Microsoft Excel
- Inglés
Supply Chain Manager (Forecasting)
Teva Pharmaceuticals —La Moraleja, Madrid provincia
- Español
- Microsoft Excel
- Inglés
Associate Director – Primary Substations (T&D)
AECOM —Madrid, Madrid provincia
- Jornada completa
- AutoCAD
- Grado
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- Vacaciones pagadas

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Associate Medical Director- Dermatology

IQVIA -
Madrid, Madrid provincia

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Detalles del empleo

Jornada completa

Cualificaciones

Desarrollo de negocios
Optimización de la conversión

Descripción completa del empleo

Madrid, Spain | Full time | Home-based | R1543307

The Associate 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
Medical Monitoring:

Primarily serves as Global 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 hours per day, 7 days per week to respond to urgent protocol-related issues at the investigative sites.
May require regular travel.
Extensive use of keyboard requiring repetitive motion of fingers.
Extensive use of telephone and face-to-face communication requiring accurate perception of speech.

Qualifications

Medical degree from an accredited and internationally recognized medical school , along with a medical license, or equivalent, from the country or region in which he/she resides and works is required.
Minimum of 5 years' experience in clinical medicine, in addition to 4 years' clinical trials experience as an investigator (Pharma, CRO, or Biotech industry).
Specialty Board certification required.
Robust and current knowledge of scientific, clinical, regulatory, commercial, and competitive landscape in applicable therapeutic area.
Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research.

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.

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associate director, alumni transition empleos en spain

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Quiero recibir la alerta de empleo más reciente de associate director, alumni transition en spain

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