Senior Clinical Development Lead / Senior Medical Safety Physician (m/f/d) — Roche
- Ort
- Basel
- Vertrag
- full-time
- Veröffentlicht
- vor 3 Tagen
Rollenüberblick
Let’s build a healthier future, together!
By combining our unique strengths, we are redefining healthcare through sustainable action and innovation.
For a behind-the-scenes look, check out this video to see how we at Roche are making personalized health care a reality.
- Let’s build a healthier future, together!
- By combining our unique strengths, we are redefining healthcare through sustainable action and innovation.
- Core responsibilities include delivering timely Medical Risk Assessments, Health Hazard Evaluations, Risk Enablers, and criteria for Potential Reportable or Safety Issues, alongside providing key clinical guidance for postmarket issues.
- Working collaboratively with experts across R&D, premarket and postmarket quality, Clinical Development, and vigilance, you act as the core medical authority and participate in Safety Board meetings.
Hauptaufgaben
- Core responsibilities include delivering timely Medical Risk Assessments, Health Hazard Evaluations, Risk Enablers, and criteria for Potential Reportable or Safety Issues, alongside providing key clinical guidance for postmarket issues.
- Working collaboratively with experts across R&D, premarket and postmarket quality, Clinical Development, and vigilance, you act as the core medical authority and participate in Safety Board meetings.
- As the Senior Clinical Development Lead / Senior Medical Safety Physician you are an independent, conscientious professional and a dedicated team player with a strong commitment to quality.
- You bring an interdisciplinary mindset, adaptability, and the confidence to make critical decisions.
- You build alignment across functions with differing priorities and inspire a positive and collaborative spirit. Your upcoming mission:
- Conduct Risk Analyses: Create comprehensive medical risk analyses (Health Hazard Evaluations, Medical Risk/Safety Assessments, and Safety Board meetings) to evaluate the clinical relevance of product complaints.
- Regulatory Communication: Process inquiries from international regulatory authorities related to adverse event reporting and product recalls.
- Expert Evaluations: Prepare internal and external medical safety evaluations and expert opinions for products across the Diagnostics portfolio (Core Lab, Molecular Lab, Near Patient Care, Diabetes Care).
- Process Optimization: Plan and conduct internal training sessions to optimize the operational interface between Customer Issue Resolution (CIR) and Medical Safety.
- Safety Board Medical Leadership: Represent Medical Safety in the internal Safety Board process, providing the medical assessment that informs board decisions.
Weitere Details
- You can read more about the history of mySugr & Roche here . Here's what we're looking for:
- You build alignment across functions with differing priorities and inspire a positive and collaborative spirit. Your upcoming mission:
- Documentation Compliance: Maintain and regularly update all procedural documents, guidelines, and SOPs/GSPs within your scope of responsibility. Essential skills for your mission:
- Medical Education & Credentials: Degree in Human Medicine (MD or equivalent); hands-on clinical experience is essential. A medical licence (or equivalent registration) is preferred.
Notizen und Originalinhalt
- You can read more about the history of mySugr & Roche here .
- Here's what we're looking for:
- You build alignment across functions with differing priorities and inspire a positive and collaborative spirit.
- Your upcoming mission:
- Documentation Compliance: Maintain and regularly update all procedural documents, guidelines, and SOPs/GSPs within your scope of responsibility.
- Essential skills for your mission:
- Medical Education & Credentials: Degree in Human Medicine (MD or equivalent); hands-on clinical experience is essential.
- A medical licence (or equivalent registration) is preferred.
Fragen zu dieser Stellenanzeige
Welches Gehalt bietet Roche für diese Stelle?
Roche gibt CHF 99'500 - 169'500 brutto pro Jahr für diese Position in Basel an. Dies ist das im Original-Inserat veröffentlichte Gehalt (oder, falls der Arbeitgeber keinen Betrag nennt, eine realistische Schätzung für Rolle und Branche) — der Rechner auf dieser Seite berechnet daraus Ihr tatsächliches Netto nach Grenzgänger-Steuer und Sozialabgaben.
Ist das eine Vollzeitstelle, und welchen Vertragstyp bietet Roche?
Diese Stelle ist eine Vollzeit-Position. Der hier angezeigte Vertragstyp stammt direkt aus dem Original-Inserat des Arbeitgebers; klären Sie genaue Arbeitszeiten, Kündigungsfrist und Probezeit während des Bewerbungsprozesses mit Roche, da diese Details auch innerhalb derselben Vertragskategorie variieren können.
Brauche ich eine Grenzgänger-Bewilligung für eine Stelle im Kanton Basel?
EU/EFTA-Bürger mit Wohnsitz in der Grenzzone des an den Kanton Basel angrenzenden Landes können eine G-Bewilligung beantragen; der Schweizer Arbeitgeber reicht sie nach Vertragsunterzeichnung beim Migrationsamt dieses Kantons ein. Grenzzonen-Regeln und Bearbeitungszeiten variieren je nach Nachbarland und Kanton — klären Sie die Details mit dem Migrationsamt des Kantons Basel oder mit HR während der Bewerbung.
Wie bewerbe ich mich für diese Stelle bei Roche?
Nutzen Sie die Schaltfläche "Jetzt bewerben" auf dieser Seite — sie führt direkt zum Original-Inserat von Roche unter roche.wd3.myworkdayjobs.com, sodass Ihre Bewerbung direkt im Bewerbermanagementsystem des Arbeitgebers landet. Frontaliere Ticino sammelt oder leitet keine Bewerbungen selbst weiter.
