12 beste Stellen als monitoring specialist in genève ge – aktuell auf Personalsuche

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PwC —Genf, GE
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- Englisch
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Spineart —Plan-les-Ouates, GE
- 100%
- Hybrides Arbeiten
- Englisch
- Produktion
- Kommunikationsfähigkeit
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Senior Data Officer for Ethiopia, based in Kampala (Link For External Applicants)
IMPACT Initiatives —Vernier, GE
- CHF 2’580 - CHF 2’640 pro Monat
- 100%
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- Urlaub aus familiären Gründen
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CERN —Genf, GE
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- 100%
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- 100%
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Sword Technologies SA —Eysins, VD
- CHF 120’000 - CHF 140’000 pro Jahr
- 100%
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Particle Accelerator Engineer (BE-OP-PSB-2026-106-LD)
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- Doktorat
- Englisch
- Ausbildung am Arbeitsplatz
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monitoring specialist jobs near genève ge

Senior Clinical Safety Specialist (EU Remote)

Cordis -
Nyon, VD

Jetzt bewerben

Details zur Stelle

100% | Pensum: 90-100%
vor 7 Stunden

Qualifikationen

Management-Erfahrung
Doktorat
Schreibfähigkeiten
Datenanalyse
Englisch
Klinische Erfahrung
Master
Projektmanagement
Risikomanagement
Kommunikationsfähigkeit

Vollständige Stellenbeschreibung

Overview:

Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs.

Responsibilities:

We are seeking a highly skilled Senior Clinical Safety Specialist with global pre-market and post-market study expertise in cardiovascular medical devices. This role is pivotal in ensuring timely review, identification and communication of safety signals for drug eluting balloons and contributing to the execution of our clinical investigations in conformity with all applicable requirements and standards. The Clinical Safety Sr. Specialist will be responsible for review, evaluation, and analysis of safety events and information from ongoing clinical studies, supporting clinical and regulatory activities across several clinical studies.

Key Responsibilities

Continuously review and analyze adverse events and safety data from ongoing clinical studies to monitor and identify any emerging safety signals or trends, potential risks, or emerging safety issues associated with the investigational products.
Investigate, manage and process all Serious Adverse Events (SAEs) for assigned clinical research trials
Support safety-related documents/sections in the clinical program development (e.g. CIP, CSR, ICF, IB, etc.)
Review, or prepare and submit, safety reports to regulatory agencies (individual or summary reports), in compliance with applicable country regulatory requirements and guidelines.
Support safety responses to address any regulatory queries or concerns related to safety signals or safety reports
Perform literature surveillance activities, develop and maintain search strategies to ensure comprehensive safety evaluations and identify any new or unexpected safety issues from published medical literature
Support regular safety review meetings and contribute to discussions on safety data interpretation, safety signal assessment and risk mitigation strategies.
Generate safety narratives for Adverse Event (AE) cases as required
Create Safety Plans as applicable
Develop DSMB and CEC charters
Oversees timelines for adverse event processing, reviews summary safety data at regular intervals and monitors CEC adjudication results.
Monitor and track all safety action items from safety oversight committees (CEC and DSMB) to ensure timely implementation of any risk mitigation strategy
Support data review and presentation development for data monitoring committee meetings
Contribute to the coding of events according to MedDRA or IMDRF standards, or review of coding.
Manage the monitoring and reporting of personal data breaches (PHI), in compliance with applicable regulations (HIPAA, GDPR)
Contribute upon request to safety documentation for marketed devices: clinical data reviews, periodic safety update reports, etc.
Strategic Impact
Support oversight of safety management for the sponsored clinical studies and commercial devices, with an initial focus on drug-eluting balloon catheters.

Key Interactions

Supervisor: Director of Global Clinical Safety
Internal Interactions: This role will interact heavily with clinical teammates across all projects and cross-functionally as needed with QA, R&D, etc.
External Customer Interactions: This role will work with DSMB and CEC members, Clinical trial physicians and research coordinators, contract research organizations, core labs, etc.

Qualifications:

Required Experience

Master’s or PhD in relevant Scientific field, or equivalent
Minimum of 4 years of relevant experience in clinical safety with global pre-market and post-market clinical trial experience within the cardiovascular medical device industry.
Safety management experience on US IDE trials
Proficiency with MedDRA (or IMDRF) and experience in safety signal detection and risk management.
Experience in safety data analysis, including analyzing trends and patterns in large datasets.
Solid understanding of FDA, ICH, GCP, SAE reporting and other global medical device regulations and safety reporting requirements.
Experience with safety reporting, guidelines, compliance and oversight across US and EU regions

Competencies & Skills

Precise, rigorous, detail-oriented with strong work ethic
Excellent communication, writing and listening skills
Demonstrates strong ability to communicate effectively cross functionally
Exhibits ability to multi-task effectively
Demonstrates solid project management skills and strong attention to detail
Self-driven and motivated
Ability to analyze, interpret, and summarize complex data
Strong problem-solving abilities
Fluent in English

Preferred Qualifications:

Cordis is proud to be an equal opportunity employer and is committed to providing equal opportunity for all teammates and applicants. At Cordis, our teammates all bring different strengths, experiences, and backgrounds, who share a passion for improving people's lives. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one’s identity. All our teammates’ points of view are key to our success, and we believe inclusion is everyone's responsibility. Together, we strive to create and maintain working and learning environments that are inclusive, equitable and welcoming.

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