20 beste Stellen als associate program – aktuell auf Personalsuche

Associate Director, Safety Ops
Denali Therapeutics —Zürich, ZH
- Bachelor
- Elektronisches Patientendossier
- Kommunikationsfähigkeit
National Consultant: MEAL and Data Management
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- Management-Erfahrung
- Englisch
- Analysefähigkeit
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Coherent Corp. —Zürich, ZH
- 100%
- Management-Erfahrung
- Wartung
- Englisch
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PwC —Zürich, ZH
- 100%
- Microsoft Powerpoint
- Microsoft Excel
- Englisch
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Idorsia Pharmaceuticals Ltd. —Basel, BS
- 100%
- Doktorat
- Englisch
- Master
4 Tage
Senior Director, European Sales (m/f/d)
Molecular Devices —Kloten, ZH
- 100%
- Homeoffice
- Oracle
- Salesforce
- Bachelor
- Bezahlte Ferien
Senior Project Manager, CMC
Vaxcyte —Visp, VS
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
2 Tage
Principal Scientist/ (Associate) Director, Medicinal Chemistry
Ridgeline Discovery —Basel, BS
- 100%
- Doktorat
- Englisch
- Kommunikationsfähigkeit
Direkt bewerben
Executive Director, International Marketing Lead – Global Atherosclerosis
MSD —Luzern, LU
- 100%
- Management-Erfahrung
- Forschungserfahrung
- Master
3 Tage
Independent Marketing Leader & Mentor
GearUp2Success —Zürich, ZH
- Homeoffice
- Führungserfahrung
Direkt bewerben
11 Tage
Marketing Manager (DACH Region)
Align Technology —Rotkreuz, ZG
- 100%
- Englisch
- Bachelor
- Marketing
Direkt bewerben
Senior Director ISC Engineering Equipment
BD —Eysins, VD
- CHF 218’200 - CHF 392’800 pro Jahr
- Homeoffice
- Management-Erfahrung
- Master
- Bachelor
Director, Toxicology
Swiss Biotech Association —Basel, BS
- Doktorat
- Forschungserfahrung
- Master
Stagiaire Food & Beverage
Marriott International, Inc —Genf, GE
- 100%
Microsoft Cloud & Digital Workplace Architect
UNION BANCAIRE PRIVÉE, UBP SA —Genf, GE
- 100%
- Microsoft Access
- Management-Erfahrung
- Windows
- Homeoffice-Möglichkeit
4 Tage
Channel Sales Engineer - DACH
Cyera —Genf, GE
- 100%
- Homeoffice
- Management-Erfahrung
- AWS
- Erfahrung mit Netzwerken
- Bezahlte Feiertage
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Business Developer - French Speaking
Ebury —Zürich, ZH
- Microsoft Excel
- Management-Erfahrung
- Vertrieb
Direkt bewerben
Apprenti(e) - Spécialiste en Restauration
Marriott International, Inc —Genf, GE
- 100%
Avionics Engineer (H/F)
Hubworkair —Basel, BS
- Wartung
- Englisch
- Microsoft Office
Mechanical Technician (SY-STI-BDE-2026-181-GRAE)
CERN —Genf, GE
- CHF 4’687 pro Monat
- 100%
- Doktorat
- CAD
- Englisch
- Ausbildung am Arbeitsplatz
Direkt bewerben
5 Tage

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Associate Director, Safety Ops

Denali Therapeutics -
Zürich, ZH

Jetzt bewerben

Details zur Stelle

Qualifikationen

Bachelor
Elektronisches Patientendossier
Kommunikationsfähigkeit

Vollständige Stellenbeschreibung

Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients.

We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.

Leads the execution and continuous improvement of global pharmacovigilance operations to ensure compliant, efficient, and high-quality safety data management across clinical and post-marketing programs. Drives cross-functional coordination and vendor oversight to support timely adverse event reporting, inspection readiness, and regulatory compliance. Contributes to the enhancement of pharmacovigilance processes and systems to support program advancement and global expansion.

Key Accountabilities / Core Job Responsibilities

Oversee global pharmacovigilance operations for assigned clinical programs
Ensure compliant safety case intake, processing, reporting, and reconciliation across all sources (including clinical studies and post-marketing sources)
Oversee safety case management activities to ensure adherence to global regulatory requirements, company procedures, and reporting timelines
Manage pharmacovigilance vendors and external partners, ensuring performance, compliance, and alignment with contractual and operational expectations
Lead the development and oversight of safety data exchange agreements (SDEA) / PV Agreements (PVA) with license partners and/or other parties
Drive continuous improvement of pharmacovigilance processes, systems, and workflows to enhance efficiency and quality
Lead the planning and operational delivery of aggregate safety reports (e.g., DSUR, PBRER, PADER)
Partner cross-functionally with Clinical, Regulatory, Safety Science, and other stakeholders to ensure effective adverse event handling and communication
Monitor pharmacovigilance compliance metrics (KPIs/KQIs), identify trends, and implement corrective and preventive actions as needed
Support regulatory inspections, audits, and inspection readiness activities, including documentation and response preparation
Contribute to the development and maintenance of pharmacovigilance procedures and training to ensure organizational awareness and compliance
Support safety-related inputs into clinical and regulatory documents (e.g., protocols, Safety Management Plans, MA submissions)
Support the implementation of safety procedures related to the company international market expansion efforts

Qualifications / Skills

Typically requires a Bachelor’s degree and 12+ years of relevant experience, or an equivalent combination of education and experience, with strong focus on pharmacovigilance safety operations in a global environment
Demonstrated expertise in global pharmacovigilance regulations and guidelines (e.g., FDA, EMA, ICH)
Experience managing vendors and external partners supporting pharmacovigilance activities
Proven ability to independently lead complex, cross-functional initiatives and manage multiple priorities
Experience supporting regulatory inspections and audits within a pharmacovigilance system
Strong communication, organizational, and problem-solving skills with ability to operate effectively in a fast-paced, matrixed environment
Experience in both pre-approval and post-marketing pharmacovigilance activities

Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a pension, medical stipend, equity and a broad range of other benefits.

Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.

Jetzt bewerben

Erweiterte Suche

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Executive Director, International Marketing Lead – Global Atherosclerosis

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Director, Toxicology

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Channel Sales Engineer - DACH

Business Developer - French Speaking

Apprenti(e) - Spécialiste en Restauration

Avionics Engineer (H/F)

Mechanical Technician (SY-STI-BDE-2026-181-GRAE)

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