20 beste vacatures voor de functie van regulatory affairs in diegem, vlg (nieuwe medewerkers gezocht)

Field Medical Manager
Sandoz —Diegem
- Voltijds
- Communicatieve vaardigheden
Associate Clinical Project Manager
IQVIA —Zaventem
- Voltijds
- Thuiswerk
- Master
- Projectmanagement
- Bachelor
Medical Advisor, Cardiovascular (Belgium)
Abacus Medicine Group —Anderlecht
- Thuiswerk
- Geneeskunde
- Doctoraat
- Master
11 dagen
Regulatory Affairs - Environment
Nipro Europe Group Companies —Mechelen
- Master
- Bachelor
- ICT
Regulatory & Public Affairs Counsel
Eneco —Mechelen
- Hybride werken
- Engels
- Ter plaatse
- Communicatieve vaardigheden
Medical Advisor, Cardiovascular (Belgium)
Abacus Medicine —Anderlecht
- Voltijds
- Thuiswerk
- Geneeskunde
- Doctoraat
- Master
11 dagen
Sr Manager EMEA Advocacy & Regulatory Intelligence
Ansell —Brussel
- Voltijds
- ICT
- Communicatieve vaardigheden
- Onderhandelen
4 dagen
Research Scientist II – Extractables & Leachables (E&L) Team Lead
Baxter —Eigenbrakel
- Onderzoek
- Managementervaring
- Communicatieve vaardigheden
- Opleidingsvergoeding CE
Public Affairs and Policy Program Manager
Google —Brussel
- € 106.000 - € 108.000 per jaar
- Onderzoek
- Bachelor
- Artificiële intelligentie
6 dagen
Patient-Centered Outcomes Research (PCOR) Lead
UCB —Eigenbrakel
- Doctoraat
- Onderzoek
- Master
Senior REACH Regulatory Compliance Consultant EMEA
The Chemours Company —Mechelen
- € 64.800 - € 140.875 per jaar
- Voltijds
- Hybride werken
- Bachelor
- ICT
- Communicatieve vaardigheden
4 dagen
Transversaal Business Process Owner - Projecten, Strategie & Regulatory Affairs
Belfius —Brussel
- Projectmanagement
- Pensioensparen
12 dagen
Environmental Regulatory Intelligence Lead
UCB —Anderlecht
- Engels
- Master
6 dagen
CQA Specialist - Benelux
Vantive —Eigenbrakel
- Geneeskunde
- ERP systemen
- Master
8 dagen
Legal Administrative Assistant
Puratos —Groot-Bijgaarden
- Voltijds
- Microsoft Powerpoint
- Microsoft Word
- Spaans
Head of Regulatory Affairs
Allianz —Brussel
- Voltijds
- Doctoraat
- Engels
- Financiën
Medical Affairs Manager COPD
GlaxoSmithKline —Waver
- € 90.750 - € 151.250 per jaar
- Voltijds
- Geneeskunde
- Communicatieve vaardigheden
13 dagen
Compliance Management Expert
skeyes —Steenokkerzeel
- Master
- Analytisch vermogen
- Communicatieve vaardigheden
Public Affairs Director, Benelux & France
UPS —Sint-Lambrechts-Woluwe
- Voltijds
Director, International Policy Research and Economics
Bristol-Myers Squibb —Eigenbrakel
- Voltijds
- Hybride werken
- Microsoft Excel
- Onderzoek
- Ter plaatse

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Field Medical Manager

Sandoz -
Diegem

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Vacaturegegevens

Voltijds

Kwalificaties

Frans
NIS
Communicatieve vaardigheden

Volledige vacaturetekst

Major accountabilities:

Expertise and Medical Support: Provides broad and deep understanding of the therapeutic area cross-functionally. Seen as credible medical and scientific expert by internal and external customers
Develops the medical strategy in line with the Sandoz strategy, propose an annual medical plan and ensure its proper deployment (clinical study, publication plan, communication plan, strategic axes of scientific partnerships, etc.).
Coordinates and ensures qualitative product / disease and therapies trainings on assigned therapy area and medicines to internal and external customers, including the field force.
Takes the responsibility of the Budget for their TA in their country
Coordinates and ensures qualitative product / disease and therapies trainings on assigned therapy area and medicines to internal and external customers, including the field force.
Organizes and leads expert committees to gather insights and enrich strategic thinking
Serves as a point of contact within the Medical Affairs team for external experts and in general in order to satisfy their needs for scientific information and knowledge in a therapeutic area relevant for Sandoz medicines, and support the safe, effective and appropriate use of Sandoz products.
Collaborates actively as member of Brand Teams with other functions (such as Marketing, Sales, Tender manager) to ensure development and implementation of material and projects part of the strategic customer plans.
Integrates the patients' point of view into all medical reflections and actions and engage as a scientific and medical partner with the medical community and patient associations within the framework of the Sandoz strategy
Develops and maintains external contacts with KOLs, influencers, key associations, academic and regulatory community to gain insights in market and clinical evolutions including competitive intelligence and organize Advisory Boards when appropriate.
Responsible for the planning of the congress strategy for their specific TA.
Engages HCP’s in non-promotional medical and scientific discussions regarding all on-market and in-development Sandoz products or topics relating to disease states.
Supports developing new data (through e.g. IITs, NIS and research collaborations), analyze existing data and distributes this internally and externally where appropriate
Provides new collaboration opportunities with HCOs and HCPs
Develops, initiates and follows up of medical projects and/or clinical studies initiated within the therapeutic area of interest for Sandoz (e.g. research collaborations).
Ensures that all material and activities are conducted with due regard to all applicable local, global and national laws, regulations, guidelines, codes of conduct, Company policies and accepted standards of best practice.

Minimum Requirements:

Advanced degree in relevant scientific discipline
Minimally 2 years of demonstrated experience in medical affairs and/or experience in a Medical Advisor/MSL function
Shows excellent presentation and communication skills to effectively convey complex medical and scientific information to diverse audiences.
Shows the ability to develop and implement effective strategies to support field medical activities, including identifying target territories, setting goals, and creating detailed action plans.
Demonstrates strong medical and scientific knowledge relevant to the product portfolio to effectively engage with healthcare professionals and internal stakeholders.
Exhibits the ability to identify and engage Key Opinion Leaders, build strong relationships, and gain insights to drive clinical advocacy and education.
Positive and ‘can-do’ approach; biased towards finding solutions and win/wins, responsiveness and flexibility.
Excellent team playing and interpersonal skills; strong sense of ownership and accountability, and proven project management
Familiar with respective health authority, GCP and ICH requirements, including regulations of promotional materials.
Successful development, implementation and management of innovative programs and processes.
Pronounced interest in commercial success of projects/products in TA/BU.
Willingness to travel a minimum of 60% in the field (Belgium – Luxembourg mainly)

Languages :

Fluent Dutch, French, English (oral and written).

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regulatory affairs vacatures in diegem, vlg

Field Medical Manager

Associate Clinical Project Manager

Medical Advisor, Cardiovascular (Belgium)

Regulatory Affairs - Environment

Regulatory & Public Affairs Counsel

Medical Advisor, Cardiovascular (Belgium)

Sr Manager EMEA Advocacy & Regulatory Intelligence

Research Scientist II – Extractables & Leachables (E&L) Team Lead

Public Affairs and Policy Program Manager

Patient-Centered Outcomes Research (PCOR) Lead

Senior REACH Regulatory Compliance Consultant EMEA

Transversaal Business Process Owner - Projecten, Strategie & Regulatory Affairs

Environmental Regulatory Intelligence Lead

CQA Specialist - Benelux

Legal Administrative Assistant

Head of Regulatory Affairs

Medical Affairs Manager COPD

Compliance Management Expert

Public Affairs Director, Benelux & France

Director, International Policy Research and Economics

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van regulatory affairs in diegem, vlg

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