20 annunci per il ruolo di regulatory specialist - switzerland (recruiting in corso)

Regulatory and Start Up Specialist - Switzerland
IQVIA —Basilea, BS
- 100%
- Remoto
- Bachelor
- Lavoro da casa
Senior Specialist, Regulatory Affairs
Travere Therapeutics —Rapperswil-Jona, SG
- 100%
- Competenze analitiche
- Bachelor
- Capacità di comunicazione
11 giorni
Senior Specialist Regulatory Affairs
Elos Medtech —Yverdon-les-Bains, VD
- 100%
- Gestionale
- Inglese
- Capacità di comunicazione
Regulatory Affairs Specialist
Helen of Troy —Losanna, VD
- 100%
- Inglese
- In presenza
- Lavoro da casa
- Convenzioni aziendali
Regulatory Operations Specialist
Axepta —Basilea, BS
- 100%
- Dottorato
- Inglese
- Master
Regulatory Reporting Specialist
Swissquote Bank —Gland, VD
- 100%
- Microsoft Excel
- Inglese
- Master
Candidatura rapida
MSL Narcolepsy - Diagnostic Pathway - (Fixed Term 12 months)
Takeda Pharmaceutical —Zurigo, ZH
- CHF 132’000 - CHF 181’500 all'anno
- 100%
- Remoto
- Dottorato
- Inglese
- Master
Clinical Research Associate, 60-100% (ID 2117)
AO Foundation —Zizers, GR
- Inglese
- Bachelor
- Cura del paziente
Specialist Neurodevelopment
Nestlé —Losanna, VD
- 100%
- Dottorato
- Inglese
- Ricerca
- Congedo parentale
- Convenzioni aziendali
Regulatory / Product Specialist
Quadrum SA —Losanna, VD
- CHF 80’000 - CHF 110’000 all'anno
- Parzialmente remoto
- SQL
- Capacità di comunicazione
- Lavoro da casa
Candidatura rapida
Clinical Training Specialist - Europe
Distalmotion SA —Epalinges, VD
- 100%
- Inglese
- Maturità liceale
- In presenza
Candidatura rapida
Regulatory Reporting Specialist (80-100%)
Lombard Odier & Cie —Ginevra, GE
- Microsoft Excel
- Inglese
- Microsoft Office
Business Transformation Specialist - Data & Analytics
Deutsche Bank —Zurigo, ZH
- 100%
- Gestionale
- Inglese
- SQL
Global Procurement Excellence Compliance Specialist
Mettler Toledo —Nänikon, ZH
- Microsoft Powerpoint
- Microsoft Excel
- Inglese
- Parcheggio libero
- Convenzioni aziendali
Global Financial Crimes Specialist
Bank of America —Zurigo, ZH
- 100%
- Bachelor
Site Start-Up Specialist based in Switzerland
Fortrea —Zurigo, ZH
- 100%
- Remoto
- Microsoft Office
- Bachelor
- Capacità di comunicazione
Device Documentation Specialist (CH)
UCB —Bulle, FR
- Gestionale
- Master
- Bachelor
Country Approval Specialist - FSP
Thermo Fisher Scientific —Home Office
- 100%
- Remoto
- Inglese
- Bachelor
- Competenze informatiche
P2624 - Global Regulatory Affairs Specialist/Manager
Debiopharm —Losanna, VD
- 100%
- Parzialmente remoto
- Dottorato
- Inglese
- Master
Candidatura rapida
EHS Specialist
Abbott Laboratories —Zurigo, ZH
- 100%
- Gestionale
- Inglese
- Master

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Regulatory and Start Up Specialist - Switzerland

IQVIA -
Basilea, BS

Candidati adesso

Dettagli della posizione

100% | Orario di lavoro: 90-100%

Benefit

Lavoro da casa

Qualifiche

Bachelor
Tedesco

Descrizione completa della posizione

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.

Candidati adesso

Perfeziona la tua ricerca

regulatory specialist offerte - switzerland

Regulatory and Start Up Specialist - Switzerland

Senior Specialist, Regulatory Affairs

Senior Specialist Regulatory Affairs

Regulatory Affairs Specialist

Regulatory Operations Specialist

Regulatory Reporting Specialist

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

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

Specialist Neurodevelopment

Regulatory / Product Specialist

Clinical Training Specialist - Europe

Regulatory Reporting Specialist (80-100%)

Business Transformation Specialist - Data & Analytics

Global Procurement Excellence Compliance Specialist

Global Financial Crimes Specialist

Site Start-Up Specialist based in Switzerland

Device Documentation Specialist (CH)

Country Approval Specialist - FSP

P2624 - Global Regulatory Affairs Specialist/Manager

EHS Specialist

Voglio ricevere gli ultimi avvisi Job Alert per il ruolo di regulatory specialist nella seguente località: switzerland

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