20 beste Stellen als associate director in zürich zh – aktuell auf Personalsuche

Associate Director, Safety Ops
Denali Therapeutics —Zürich, ZH
- Elektronisches Patientendossier
- Kommunikationsfähigkeit
Associate Director, Global Medical Affairs Rare Haemato-Renal Disorders
Novo Nordisk —Zürich, ZH
- Doktorat
- Projektmanagement
- Vor Ort
1 Tag
Associate Program Director, Dravet
Biogen —Baar, ZG
- 100%
- Analysefähigkeit
- Projektmanagement
- Führungserfahrung
7 Tage
Associate Director, Global Patient Finding
Biogen —Baar, ZG
- 100%
- Management-Erfahrung
- Master
- Projektmanagement
ICOE FA Associate Director Field Content Creation
Biogen —Baar, ZG
- 100%
- Doktorat
- Analysefähigkeit
- Projektmanagement
- Bezahlte Feiertage
- Eltern-/Erziehungsurlaub
Associate to the Directors at ETH AI Center
ETH Zürich —Zürich, ZH
- Teilzeit
- Management-Erfahrung
- Forschungserfahrung
- Master
Associate Director EU CTR Strategy & Operations Excellence Lead
Biogen —Baar, ZG
- 100%
- Management-Erfahrung
- Projektmanagement
- Führungserfahrung
5 Tage
Associate Director, Pharmacokinetics (PK)
CSL Behring —Glattbrugg, ZH
- 100%
- Doktorat
- Projektmanagement
- Führungserfahrung
Associate Director, Biostatistics
CSL Vifor —Glattbrugg, ZH
- 100%
- Doktorat
- Englisch
- Master
Associate Director, Global Regulatory Strategy (GRS) (m/f/d)
GlaxoSmithKline —Baar, ZG
- 100%
- Doktorat
- Schreibfähigkeiten
- Bachelor
Sr Manager / Associate Director Regulatory Affairs - Swiss Affiliate
Gilead Sciences —Zug, ZG
- 100%
- Management-Erfahrung
- Englisch
- Bachelor
Associate Director, Quality
Kiniksa Pharmaceuticals —Zug, ZG
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Direkt bewerben
Regulatory Strategy Associate Director
Vertex Pharmaceuticals —Zug, ZG
- 100%
- Doktorat
- Englisch
- Master
Associate Director, Biostatistics (2)
CSL Behring —Glattbrugg, ZH
- 100%
- Doktorat
- Datenanalyse
- Englisch
Sr Director, Country & Site Operations (CSO)
Biogen —Baar, ZG
- 100%
- Management-Erfahrung
- Projektmanagement
- Bachelor
2 Tage
Associate Director, Statistical Programming (w/m/d)
CSL Behring —Glattbrugg, ZH
- 100%
- Wartung
- Englisch
- Bachelor
13 Tage
Director, Europe Patient Advocacy, Professional Relations, and Patient Engagement
Genmab —Zug, ZG
- Wochenendarbeit
- Doktorat
- Englisch
- Master
Director Work, Rewards & Careers
WTW —Zürich, ZH
- 100%
- Englisch
- Microsoft Office
- Analysefähigkeit
Associate (m/f/d) - Global Transaction Advisory Group
Alvarez & Marsal —Zürich, ZH
- Microsoft Powerpoint
- Microsoft Excel
- Englisch
Academic Associate Chemistry and Business Studies
Universität Zürich —Zürich, ZH
- 100%
- Management-Erfahrung
- Doktorat
- Englisch
- Weiterbildungen

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Associate Director, Safety Ops

Denali Therapeutics -
Zürich, ZH

Jetzt bewerben

Details zur Stelle

Qualifikationen

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 Bachelorâ€™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 candidateâ€™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. Â

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

associate director Jobs in zürich zh

Associate Director, Safety Ops

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Associate Director, Global Patient Finding

ICOE FA Associate Director Field Content Creation

Associate to the Directors at ETH AI Center

Associate Director EU CTR Strategy & Operations Excellence Lead

Associate Director, Pharmacokinetics (PK)

Associate Director, Biostatistics

Associate Director, Global Regulatory Strategy (GRS) (m/f/d)

Sr Manager / Associate Director Regulatory Affairs - Swiss Affiliate

Associate Director, Quality

Regulatory Strategy Associate Director

Associate Director, Biostatistics (2)

Sr Director, Country & Site Operations (CSO)

Associate Director, Statistical Programming (w/m/d)

Director, Europe Patient Advocacy, Professional Relations, and Patient Engagement

Director Work, Rewards & Careers

Associate (m/f/d) - Global Transaction Advisory Group

Academic Associate Chemistry and Business Studies

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