20 publicaciones de empleo destacadas de associate director, regulatory affairs en martorelles, ct (¡Están contratando!)

Associate Director, Medical Affairs
Alcon —Cornellà de Llobregat, Barcelona provincia
- Jornada completa
- Doctorado
- Inglés
- Investigación
Senior Project Manager / Associate Project Management Director
Optimapharm d.o.o. —Barcelona, Barcelona provincia
- De 80.000 € a 100.000 € al año
- Jornada completa
- Teletrabajo
- Inglés
- Investigación
- Máster
Regional Regulatory Affairs Head – Badalona
Menarini —Badalona, Barcelona provincia
- De lunes a viernes
- Trabajo híbrido
- Español
- Mantenimiento
- Inglés
Executive Director, Regulatory Affairs Strategy - Cell Therapy
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Oficina
- Habilidades de presentación
Regulatory Affairs Specialist
Grifols SA —Sant Cugat del Vallès, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Español
- Microsoft Excel
- Inglés
Associate Director, Territory Operations Manager - Cell Therapy
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- CRM software
- Español
- Microsoft Excel
ASSOCIATE DIRECTOR, REGULATORY AFFAIRS
Almirall —Sant Feliu de Llobregat, Barcelona provincia
- Jornada completa
- Inglés
- Project management
- Grado
Development Tech Transformation PMO - Associate Director
Novartis —Barcelona, Barcelona provincia
- De 63.600 € a 118.000 € al año
- Jornada completa
- Máster
- Grado
- Administración y dirección de empresas
CMC Biopharma Regulatory Consultant — Ecolab Life Sciences
Ecolab —Barcelona, Barcelona provincia
- 7.425 € al mes
- Jornada completa
- Doctorado
- Ventas
- Máster
POSITION REGULATORY AFFAIRS SPECIALIST
FARMHISPANIA GROUP —Barcelona, Barcelona provincia
- Inglés
- APIs
Associate Director, IMACE Scientific Content, NS
Novartis —Barcelona, Barcelona provincia
- De 73.100 € a 135.700 € al año
- Jornada completa
- Doctorado
- Inglés
- Liderazgo
Associate Director / Associate Principal, Patient-centered Mixed Methods, Survey & Implementation Science Research
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Doctorado
- Inglés
- Investigación
Director, Regulatory Affairs Strategy - Cell Therapy
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Oficina
- Habilidades de presentación
Regulatory Affairs Technician (LATAM) – Badalona
Menarini —Badalona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
Sr Director, Drug Development Lead
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Doctorado
- Teletrabajo opcional
3d
Associate Director, Adoption Strategy & Enablement
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Máster
- Grado
3d
Product Stewardship & Regulatory Compliance Specialist (m/f/d) Europe & Asia
Westlake Global Compounds —Santa Perpètua de Mogoda, Barcelona provincia
- Jornada completa
- Inglés
Solicitud rápida
14d
Senior Quality & Regulatory Compliance Manager - Medical and In Vitro Devices
Sener —Cerdanyola del Vallès, Barcelona provincia
- Trabajo híbrido
- Español
- Grado
Solicitud rápida
Associate Director, Global Knowledge Management
CSL Behring —Barcelona, Barcelona provincia
- Jornada completa
- Doctorado
- Inglés
- Investigación
1h
Senior Staff - Medical & Scientific Affairs Liaison - Acute Care
Beckman Coulter Diagnostics —Barcelona, Barcelona provincia
- Jornada completa
- Doctorado
- Ventas
- Investigación
- Vacaciones pagadas

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Associate Director, Medical Affairs

Alcon -
Cornellà de Llobregat, Barcelona provincia

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Detalles del empleo

Jornada completa

Cualificaciones

Investigación clínica
Doctorado
Inglés
Investigación
Máster
Grado

Descripción completa del empleo

At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us?

This role is part of Alcon's Research & Development function, a team that innovates boldly and delivers new products and services to help revolutionize the eye care industry, advance optimal patient outcomes and help people see brilliantly. The Associate Director, Medical Affairs is primarily responsible for driving the medical strategy for surgical product development in Ophthalmology, focusing on strategy development, management, and implementation for Phase IIIB/IV studies. You will build relationships with global development teams, marketing, sales, and healthcare providers to meet diverse needs.

In this role, a typical day will include:

Support the execution of comprehensive Medical Affairs strategic plans

Support development of regional medical affairs strategy for the assigned therapeutic area

Provide medical and scientific support for product messaging and claims development

Support post market/phase IV studies strategy and preregistration study strategic input

Support launch strategies, lifecycle management and expansion of indications

for use

Support medical publications: Develop content for whitepapers, peer-reviewed

manuscripts, posters, scientific articles and video scripts

Support customer medical inquires (i.e. medical exchange of information with

KOLs, and management of medical issues raised by customer HealthCare

providers)

Maintain peer to peer relationships with Medical Experts/ Key stakeholders and members of the scientific community, utilizing scientific and medical evidence based non-promotional materials

Support planning and execution of medical advisory board meetings

Provide fairbalanced scientific and educational information to healthcare professionals on specific medical issues

Support internal training, and as needed for academic or healthcare professionals

Medical promotional review support as needed

WHAT YOU’LL BRING TO ALCON:

Bachelor’s Degree or Equivalent years of directly related experience (or high

school+15 yrs; Assoc.+14 yrs; M.S.+7 yrs; PhD+6 yrs)

Advanced clinical degree (OD preferred; MD ophthalmologist preferred) in combination strong clinical research experience. Minimum: technical/scientific degree (i.e.MS/PhD) in the life sciences with solid knowledge in assigned ophthalmic therapeutic area.

7 Years of Relevant Experience

The ability to fluently read, write, understand and communicate in English

Estimated travel requirements - 10%

The location of the position is flexible within Europe.

HOW YOU CAN THRIVE AT ALCON:

Manage your own workload and schedule while hitting your set targets
Collaborate with teammates to share best practices and learnings as work evolves
See your career like never before with focused growth and development opportunities

Alcon Careers

See your impact at alcon.com/careers

ATTENTION: Current Alcon Employee/Contingent Worker

If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.

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associate director, regulatory affairs empleos en martorelles, ct

Associate Director, Medical Affairs

Senior Project Manager / Associate Project Management Director

Regional Regulatory Affairs Head – Badalona

Executive Director, Regulatory Affairs Strategy - Cell Therapy

Regulatory Affairs Specialist

Associate Director, Territory Operations Manager - Cell Therapy

ASSOCIATE DIRECTOR, REGULATORY AFFAIRS

Development Tech Transformation PMO - Associate Director

CMC Biopharma Regulatory Consultant — Ecolab Life Sciences

POSITION REGULATORY AFFAIRS SPECIALIST

Associate Director, IMACE Scientific Content, NS

Associate Director / Associate Principal, Patient-centered Mixed Methods, Survey & Implementation Science Research

Director, Regulatory Affairs Strategy - Cell Therapy

Regulatory Affairs Technician (LATAM) – Badalona

Sr Director, Drug Development Lead

Associate Director, Adoption Strategy & Enablement

Product Stewardship & Regulatory Compliance Specialist (m/f/d) Europe & Asia

Senior Quality & Regulatory Compliance Manager - Medical and In Vitro Devices

Associate Director, Global Knowledge Management

Senior Staff - Medical & Scientific Affairs Liaison - Acute Care

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