20 beste vacatures voor de functie van regulatory affairs environment in brussels, bru (nieuwe medewerkers gezocht)

Patient-Centered Outcomes Research (PCOR) Lead
UCB —Eigenbrakel
- Doctoraat
- Onderzoek
- Master
Medical Advisor, Cardiovascular (Belgium)
Abacus Medicine Group —Anderlecht
- Thuiswerk
- Geneeskunde
- Doctoraat
- Master
13 dagen
Drug Safety Advisor
Qplus consult —Melsbroek
- Doctoraat
- Master
EMEA GAPP Policy and Campaigns Executive, YouTube (English)
YouTube —Brussel
- € 106.000 - € 108.000 per jaar
- Bachelor
- Ter plaatse
6 dagen
EU Regulatory Strategy Team Lead
UCB —Anderlecht
- Doctoraat
- Master
Associate Consultant, Tech Policy
APCO Worldwide —Brussel
- Schrijfvaardigheden
- Projectmanagement
- Artificiële intelligentie
Project Manager Generalist | Life Science
Capgemini Sogeti —Diegem
- PMP
- Projectmanagement
Site Conformance Expert | Life Science
Capgemini Sogeti —Diegem
- € 50.000 per jaar
- Master
- Communicatieve vaardigheden
12 dagen
Site Conformance Expert | Life Science
Capgemini —Diegem
- € 50.000 per jaar
- Master
- Communicatieve vaardigheden
12 dagen
Digital Technology Lead Medical Affairs
UCB —Anderlecht
- Engels
- Master
DT Medical Affairs Lead
UCB —Anderlecht
- Master
- Bachelor
Medical Affairs Manager COPD
GlaxoSmithKline —Waver
- € 90.750 - € 151.250 per jaar
- Voltijds
- Geneeskunde
- Communicatieve vaardigheden
14 dagen
Senior Manager EU Affairs
International Air Transport Association (IATA) —Brussel
- Hybride werken
- Analytisch vermogen
6 dagen
Research Executive
Rud Pedersen Public Affairs Company AB —Brussel
- Stage
1 dag
Legal Administrative Assistant
Puratos —Groot-Bijgaarden
- Voltijds
- Microsoft Powerpoint
- Microsoft Word
- Spaans
Director, EU Public Affairs
Bavarian Nordic —Brussel
- Voltijds
- Verhuiskostenvergoeding
9 dagen
Associate Partner - Governance
AION Consulting —Brussel
- Master
- Bedrijfsontwikkeling
(Senior) Managing Director - Public Affairs
Burson Global —Brussel
- Hybride werken
- Microsoft Excel
- Engels
- Artificiële intelligentie
Public Policy Manager (all genders) in Brussels
Ridedott —Brussel
- € 50.000 - € 70.000 per jaar
- Voltijds
- Thuiswerk
- Master
- Projectmanagement
- Onderhandelen
Director, International Policy Research and Economics
Bristol-Myers Squibb —Eigenbrakel
- Voltijds
- Hybride werken
- Microsoft Excel
- Onderzoek
- Ter plaatse

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van regulatory affairs environment in brussels, bru

Door in te loggen op je account, ga je akkoord met de Algemene voorwaarden van SimplyHired en stem je in met ons Cookie- en privacybeleid.

Zoek vacatures in meer locaties

regulatory affairs environment jobs near brussels, bru

Vacatures voor een Stage Data Science in Brussels

Vacatures voor een Recruitment Consultant in Bruxelles

Vacatures voor een Vebego Cleaning & Services in Zaventem

Vacatures voor een Group Cleaning Services in Sint Lambrechts Woluwe

Vacatures voor een Food Technology in Bruxelles

Vacatures voor een Lead Architect in Bruxelles Schaarbeek

Vacatures voor een Technology Lead in Eigenbrakel

Vacatures voor een Chief Technology Officer in Ghent

Vacatures voor een Public Health in Bruxelles

Vacatures voor een Eu Government Affairs in Bruxelles

Vacatures voor een Senior Designer in Bruxelles

Vacatures voor een Senior Product Manager in Antwerpen

Vacatures voor een Manager in Kortrijk

Vacatures voor een Manager Leidinggevende Functie in Limburg (provincie)

Vacatures voor een Junior Researcher in Bruxelles

Vacatures voor een Researcher in Brussel

Vacatures voor een Legal Assistant in Huldenberg Neerijse

Vacatures voor een Legal Assistant in Melle Gontrode

Vacatures voor een Assistant Social in Haren

Vacatures voor een Legal Assistant in Retie

Patient-Centered Outcomes Research (PCOR) Lead

UCB -
Eigenbrakel

Nu solliciteren

Vacaturegegevens

Vaste Jobs

Kwalificaties

Doctoraat
Onderzoek
Master
Managementervaring

Volledige vacaturetekst

Make your mark for patients

We are looking for a Patient-Centered Outcomes Research (PCOR) Lead who is strategic, collaborative, and insightful to join our Patient-Centered Outcomes Research (PCOR) team, based at our UCB headquarter located in Brussels, Belgium, or in our offices in Monheim Germany, or Slough UK.

About the role

As a PCOR Lead, you will play a leading role in the development and implementation of patient-reported outcomes (PRO) and more broadly clinical outcome assessment (COA) strategies. You will generate robust patient experience data and evidence that demonstrate the meaningful patient benefits of our innovative UCB solutions and that meet external evidentiary standards and support healthcare decision-making.

Who you will work with

As a member of the Patient-Centered Outcomes Research team, you will collaborate with cross-functional teams, eg, representatives from Clinical Development, Medical Affairs, Health Economics and Outcomes Research, Market Access, Regulatory Affairs, and Biostatistics.

What you will do

You will lead the development and implementation of patient experience evidence strategy on clinical outcome assessments (COAs) from early development through to full lifecycle management.
You will lead research activities supporting the selection, development, validation, interpretation, and implementation of PRO/COA measures.
You will provide subject matter expert input into strategic documents, tactical plans and target patient value profiles, as well as into clinical documents, eg, study protocols, analysis plans, clinical reports.
You will provide subject matter expert input into regulatory and HTA briefing packages and interactions..
You will lead scientific dissemination (eg, peer-reviewed publications, abstracts) in line with publication strategies.
You will build relationships and partner with external groups to advance methodological frameworks and acceptance of patient experience evidence to inform external healthcare decision making.
You will be an inspiring ambassador to contribute to organizational awareness on the value of patient experience evidence.

Interested? For this role, we are looking for the following education, experience, and skills:

Master's degree, PhD, MD, or equivalent qualification in a relevant scientific discipline.
Significant experience in biopharmaceutical, medical device, or academic environments within PRO/COA, or patient preference research.
Expertise in PRO/COA development, validation, and implementation in clinical research, including strong knowledge of qualitative and quantitative scientific methodologies and evidentiary requirements by regulatory and HTA bodies
Experience in clinical development, regulatory and HTA interactions.
Excellent stakeholder management, communication, influencing, and cross-functional collaboration skills in a matrix organization.
Proven project leadership capabilities with experience managing complex global initiatives

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on [email protected]. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Nu solliciteren

Verfijn je zoekopdracht

regulatory affairs environment vacatures in brussels, bru

Patient-Centered Outcomes Research (PCOR) Lead

Medical Advisor, Cardiovascular (Belgium)

Drug Safety Advisor

EMEA GAPP Policy and Campaigns Executive, YouTube (English)

EU Regulatory Strategy Team Lead

Associate Consultant, Tech Policy

Project Manager Generalist | Life Science

Site Conformance Expert | Life Science

Site Conformance Expert | Life Science

Digital Technology Lead Medical Affairs

DT Medical Affairs Lead

Medical Affairs Manager COPD

Senior Manager EU Affairs

Research Executive

Legal Administrative Assistant

Director, EU Public Affairs

Associate Partner - Governance

(Senior) Managing Director - Public Affairs

Public Policy Manager (all genders) in Brussels

Director, International Policy Research and Economics

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van regulatory affairs environment in brussels, bru

Related Searches

Zoek vacatures in meer locaties

Tools voor werkzoekenden

Werkgeverstools

Bladeren

Blijf verbonden