20 meilleures offres (regulatory specialist, switzerland) (à pourvoir)

Regulatory and Start Up Specialist - Switzerland
IQVIA —Bâle, BS
- 100%
- Télétravail
- Niveau Licence
- Travail à domicile
Senior Specialist, Regulatory Affairs
Travere Therapeutics —Rapperswil-Jona, SG
- 100%
- Esprit d'analyse
- Niveau Licence
- Compétences en communication
il y a 11 jours
Regulatory Affairs Specialist
Helen of Troy —Lausanne, VD
- 100%
- Anglais
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- Réduction pour les employés
Senior Specialist Regulatory Affairs
Elos Medtech —Yverdon-les-Bains, VD
- 100%
- Gestion du personnel
- Anglais
- Compétences en communication
Regulatory Reporting Specialist
Swissquote Bank —Gland, VD
- 100%
- Microsoft Excel
- Anglais
- Niveau Master
Postuler rapidement
Regulatory Operations Specialist
Axepta —Bâle, BS
- 100%
- Niveau Doctorat
- Anglais
- Niveau Master
Regulatory / Product Specialist
Quadrum SA —Lausanne, VD
- De 80 000 CHF à 110 000 CHF par an
- Travail hybride
- SQL
- Compétences en communication
- Travail à domicile
Postuler rapidement
Clinical Research Associate, 60-100% (ID 2117)
AO Foundation —Zizers, GR
- Anglais
- Niveau Licence
- Soins aux patients
Clinical Training Specialist - Europe
Distalmotion SA —Epalinges, VD
- 100%
- Anglais
- Maturité
- En présentiel
Postuler rapidement
Specialist Neurodevelopment
Nestlé —Lausanne, VD
- 100%
- Niveau Doctorat
- Anglais
- Recherche
- Jours fériés payés
- Congé parental payé
Regulatory Reporting Specialist (80-100%)
Lombard Odier & Cie —Genève, GE
- Microsoft Excel
- Anglais
- Microsoft Office
MSL Narcolepsy - Diagnostic Pathway - (Fixed Term 12 months)
Takeda Pharmaceutical —Zürich, ZH
- De 132 000 CHF à 181 500 CHF par an
- 100%
- Télétravail
- Niveau Doctorat
- Anglais
- Niveau Master
Business Transformation Specialist - Data & Analytics
Deutsche Bank —Zürich, ZH
- 100%
- Gestion du personnel
- Analyse de données
- Anglais
P2624 - Global Regulatory Affairs Specialist/Manager
Debiopharm —Lausanne, VD
- 100%
- Travail hybride
- Niveau Doctorat
- Anglais
- Niveau Master
Postuler rapidement
Country Approval Specialist - FSP
Thermo Fisher Scientific —Home Office
- 100%
- Télétravail
- Anglais
- Niveau Licence
- Bureautique
Global Procurement Excellence Compliance Specialist
Mettler Toledo —Nänikon, ZH
- Microsoft Powerpoint
- Microsoft Excel
- Anglais
- Stationnement gratuit
- Réduction pour les employés
Device Documentation Specialist (CH)
UCB —Bulle, FR
- Gestion du personnel
- Niveau Master
- Niveau Licence
EHS Specialist
Abbott Laboratories —Zürich, ZH
- 100%
- Gestion du personnel
- Anglais
- Niveau Master
Senior Privacy & AI Governance Specialist (temporary position)
SIX Group AG —Zürich, ZH
- Temps partiel
- Télétravail
- Gestion du personnel
- Anglais
- Compétences en communication
Global Financial Crimes Specialist
Bank of America —Zürich, ZH
- 100%
- Niveau Licence

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Regulatory and Start Up Specialist - Switzerland

IQVIA -
Bâle, BS

Soumettre votre candidature

Détails de l'emploi

100% | Temps de travail : 90-100%

Avantages

Travail à domicile

Qualifications

Expérience clinique
Niveau Licence
Allemand

Description complète du poste

Basel, Switzerland | Full time | Home-based | R1559742

Job Overview
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.

Home Based position requiring German language fluency.

Essential Functions
Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.

Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
Perform start up and site activation activities according to applicable regulations, SOPs and work instructions.

Distribute completed documents to sites and internal project team members.
Prepare site regulatory documents, reviewing for completeness and accuracy.
Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
Review and provide feedback to management on site performance metrics.
Review, establish and agree on project planning and project timelines.

Ensure monitoring measures are in place and implement contingency plan as needed.
Inform team members of completion of regulatory and contractual documents for individual sites.
Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.
Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
Perform quality control of documents provided by sites.
May have direct contact with sponsors on specific initiatives.

Qualifications
Bachelor’s Degree in life sciences or a related field and 3 years’ clinical research or other relevant experience; or equivalent combination of education, training and experience.

In-depth knowledge of clinical systems, procedures, and corporate standards.
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
Knowledge of applicable regulatory requirements, including local regulations, , SOPs and company’s Corporate Standards.
Understanding of regulated clinical trial environment and knowledge of drug development process.

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.

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.

Soumettre votre candidature

Affinez votre recherche

regulatory specialist emplois - switzerland

Regulatory and Start Up Specialist - Switzerland

Senior Specialist, Regulatory Affairs

Regulatory Affairs Specialist

Senior Specialist Regulatory Affairs

Regulatory Reporting Specialist

Regulatory Operations Specialist

Regulatory / Product Specialist

Clinical Research Associate, 60-100% (ID 2117)

Clinical Training Specialist - Europe

Specialist Neurodevelopment

Regulatory Reporting Specialist (80-100%)

MSL Narcolepsy - Diagnostic Pathway - (Fixed Term 12 months)

Business Transformation Specialist - Data & Analytics

P2624 - Global Regulatory Affairs Specialist/Manager

Country Approval Specialist - FSP

Global Procurement Excellence Compliance Specialist

Device Documentation Specialist (CH)

EHS Specialist

Senior Privacy & AI Governance Specialist (temporary position)

Global Financial Crimes Specialist

Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : regulatory specialist (switzerland)

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