20 meilleures offres (regulatory specialist, eysins vd) (à pourvoir)

Regulatory and Start Up Specialist - Switzerland
IQVIA —Eysins, VD
- 100%
- Télétravail
- Niveau Licence
- Travail à domicile
Regulatory Reporting Specialist
Swissquote Bank —Gland, VD
- 100%
- Microsoft Excel
- Anglais
- Niveau Master
Postuler rapidement
Regulatory Reporting Specialist (80-100%)
Lombard Odier & Cie —Genève, GE
- Microsoft Excel
- Anglais
- Microsoft Office
Team Head, Emerging Markets Documentation Specialists (f/m/x)
Deutsche Bank —Genève, GE
- 100%
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical & Regulatory Affairs Specialist
Axepta —Plan-les-Ouates, GE
- Compétences rédactionnelles
- Anglais
Payment Specialist (80-100%) (12-month contract)
Lombard Odier & Cie —Genève, GE
- Anglais
- Esprit d'analyse
- Technologies de l'information
Shipping Coordinator
Sotheby's —Genève, GE
- Heures supplémentaires
- Anglais
- Niveau Master
- Niveau Licence
Client Reporting Product Lead
Barclays —Genève, GE
- Gestion du personnel
- Esprit d'analyse
- Sens de l'organisation
il y a 3 jours
Clinical Imaging Specialist - EU
Anteris Technologies —Genève, GE
- Télétravail
- Microsoft Powerpoint
- Microsoft Word
- Anatomie
Postuler rapidement
Trader - Bonds & Structured Products
SYZ GROUP —Genève, GE
- Microsoft Excel
- Gestion du personnel
- Anglais
Senior Cash Projects & Coordination Manager
UNION BANCAIRE PRIVÉE, UBP SA —Genève, GE
- 100%
- Microsoft Powerpoint
- Microsoft Excel
- Anglais
Senior Consultant - Regulatory & Compliance FS 80-100% (f/m/d)
Grant Thornton —Genève, GE
- Anglais
- Niveau Licence
Relationship Manager - Global South Asia & Africa
Deutsche Bank —Genève, GE
- 100%
- Gestion du personnel
il y a 13 jours
Investment Specialist
PICTET —Genève, GE
- Microsoft Powerpoint
- Microsoft Excel
- Gestion du personnel
Risk Manager
EFG International —Genève, GE
- Microsoft Excel
- Anglais
- Microsoft Office
il y a 9 jours
Principal Client Advisor
World Intellectual Property Organization —Genève, GE
- De 64 121 CHF à 118 431 CHF par an
- Espagnol
- Service client
- Anglais
- Formation sur place
il y a 6 jours
Risk & Compliance Analytics Engineer
PICTET —Genève, GE
- Anglais
- Niveau Master
- SQL
il y a 12 jours
Appway Support & Development Specialist
Sword Services —Genève, GE
- 100%
- Travail hybride
- Gestion du personnel
- Dépannage logiciel
- Anglais
Postuler rapidement
Manager - Regulatory & Compliance FS 80-100% (f/m/d)
Grant Thornton —Genève, GE
- Anglais
- Niveau Licence
HRIS Onboarding Intern
Richemont —Meyrin, GE
- 100%

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Regulatory and Start Up Specialist - Switzerland

IQVIA -
Eysins, VD

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

Eysins, 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 - eysins vd

Regulatory and Start Up Specialist - Switzerland

Regulatory Reporting Specialist

Regulatory Reporting Specialist (80-100%)

Team Head, Emerging Markets Documentation Specialists (f/m/x)

Clinical & Regulatory Affairs Specialist

Payment Specialist (80-100%) (12-month contract)

Shipping Coordinator

Client Reporting Product Lead

Clinical Imaging Specialist - EU

Trader - Bonds & Structured Products

Senior Cash Projects & Coordination Manager

Senior Consultant - Regulatory & Compliance FS 80-100% (f/m/d)

Relationship Manager - Global South Asia & Africa

Investment Specialist

Risk Manager

Principal Client Advisor

Risk & Compliance Analytics Engineer

Appway Support & Development Specialist

Manager - Regulatory & Compliance FS 80-100% (f/m/d)

HRIS Onboarding Intern

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

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