Director - (Senior) Patient Safety Physician (gn): Oncology für München gesucht
Arbeits- und Stellenangebot im Regiobizz Arbeitsmarkt
Job Kategorie: Personalberatung/Arbeitsvermittlung Personalwesen/HR
Stellenangebot Basisdaten
- Arbeitsort:
-
DE 81539 München
- Umkreis:
-
keine Angabe.
- Art der Arbeitsstelle:
-
- Letze Aktualisierung:
-
13.11.20242024-11-13
Stellenausschreibung: Director - (Senior) Patient Safety Physician (gn): Oncology
- Arbeitgeber bzw.
Arbeitsvermittler
-
ageneo Life Science Experts GmbH in Hamburg
- Branche
-
Personalberatung/Arbeitsvermittlung
- Kategorie
-
Personalwesen/HR
- Stellenbeschreibung
- Ãœber uns For a globally leading (bio)pharmaceutical company, we are
assigned to recruit a Director Patient Safety (gn) for the therapeutic
area Oncology. Your primary focus will revolve around orchestrating
the global initiatives for Patient Safety and Pharmacovigilance (PSPV)
and Risk Management (RM) pertaining to compounds at various stages of
development. In this role, you will work closely with the clinical
development department and will be involved in a very strategic and
global function. Aufgaben Crafting proactive, patient-centric RM
strategies tailored to designated compounds. Overseeing and executing
all PV activities pertinent to assigned drugs, encompassing database
setup, continual safety monitoring, and addressing safety concerns.
Engaging in cross-functional collaboration with departments such as
Clinical Development and Global Patient Engagement to devise
patient-centric benefit-risk evaluations for developmental compounds.
Collaborating with Global Epidemiology and Medical Affairs to design
safety-oriented post-authorization studies. Analyzing clinical trial
safety data for incorporation into clinical trial reports and
regulatory submissions. Providing medical-scientific insights into
regulatory documents, including PSURs, DSURs, RMPs, and Clinical
Overview Statements. Chair multidisciplinary Benefit Risk Teams
Keeping senior management apprised of the safety profile of designated
drugs and suggesting PV/RM actions Profil Medical degree with clinical
and/or clinical research experience. Proficient knowledge in
pharmacovigilance (PV) and a comprehensive understanding of PV
regulations in major markets. Experience in clinical development and
involvement in regulatory submissions would be advantageous. In-depth
understanding of the pharmaceutical industry, future trends and
developments in pharmacovigilance Practical understanding of PV
regulation in major markets and respective need for compliance
Clinical or research experience in oncology are a big plus. Strong
interpersonal and communication skills. Strong ethical sense coupled
with a focus on quality and patient safety. Excellent English language
skills, both written and verbal. Wir bieten highly strategic and
development-related role high-impact on the development of new drugs
global and intercultural work environment
- Qualifikation
- Arbeitskräfte
- Verdienst:
- n.a.
- Bewerbung an
- ageneo Life Science Experts GmbH
Am Strandkai 1
De 20457 Hamburg
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