Salaire moyen: CHF102 213 /annuel
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- ...chez la patientèle vulnérable (enfants, personnes âgées, psychiatriques). Le service est le centre régional de référence pour la pharmacovigilance. Il assure par ailleurs une prise en charge multidisciplinaire reconnue dans le domaine de la douleur. Dans l'ensemble de ces...Suggéré
- ...subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. Conducts Source Document...SuggéréTravail intérimRemote jobRecrutement immédiat
- ...details and innovation, strong organizational and communication skills. Responsibilities ~ Perform medical monitoring and pharmacovigilance activities (such as medical oversight of the study, eligibility checks, review safety data) ~ Provide causality assessments...SuggéréTemps pleinà domicileNoëlTravail à domicileHoraire flexible
- ...stakeholders and cross‑functional Program Teams, including Clinical Development, Clinical Operations, Biometrics, Nonclinical, Pharmacovigilance, Quality, Regulatory CMC, Regulatory Labelling, Regulatory Project Management, Medical Writing, corporate partners, and...Suggéré
- ...Work closely with the Lysates Team on strategy development and drive the implementation of product strategies * Contribute to pharmacovigilance by assisting with the transmission and processing of Adverse Drug Reactions (ADRs) * Support the Regulatory and Market access...SuggéréTemps plein
- ...compliance with GVP, GCP and global regulatory requirements. The GPSSL works collaboratively with other members of the Sobi Global Pharmacovigilance team, and other internal functions across Sobi or externally to ensure proactive safety management, high‑quality regulatory...SuggéréTemps plein
CHF 133700 par année
...Medicine, Pharmacy, or a related scientific discipline. ~ Extensive experience in clinical development, quality assurance, pharmacovigilance, or regulated healthcare environments. ~ Proven leadership experience building, developing, and leading global teams...SuggéréHoraire flexible- ...negotiations with Regulatory Authorities. · Knowledge in quality assurance, promotional and non-promotional review as well as Pharmacovigilance and market access are advantageous. · Excellent working knowledge regarding national/regional Regulatory Authorities...SuggéréTemps plein
- ...Associate Safety Director with at least 4 years of drug development experience, including a minimum of 3 years in drug safety/pharmacovigilance. The job requires on-site presence in Basel (Switzerland), and the initial contract duration is 12 months. Your Main...Suggéré
- ...proactive safety management. Your responsibilities ~ Ensure implementation of GVP compliant PV standards, processes by the Pharmacovigilance Scientists, Device expert, and Medical coding expert under their management and conducts cross-functional collaboration with...Suggéré

