Senior Clinical Development Lead / Senior Medical Safety Physician (m/f/d) — Roche
- Lieu
- Basel
- Contrat
- full-time
- Publié
- il y a 4 jours
Vue d’ensemble du poste
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.
Responsabilités principales
- 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.
Détails supplémentaires
- 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.
Notes et contenu original
- 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.
Questions sur cette offre
Quel salaire propose Roche pour ce poste ?
Roche indique CHF 99 500 - 169 500 bruts par an pour ce poste à Basel. Il s'agit du salaire publié dans l'annonce d'origine (ou, si l'employeur ne précise pas de montant, d'une estimation réaliste pour le rôle et le secteur) — le calculateur de ce site le convertit en net réel une fois l'impôt frontalier et les cotisations sociales appliqués.
Est-ce un poste à temps plein, et quel type de contrat propose Roche ?
Cette offre est un poste en temps plein. Le type de contrat affiché ici provient directement de l'annonce originale de l'employeur ; confirmez toujours les horaires exacts, le préavis et la durée d'essai avec Roche pendant le processus de candidature, ces détails pouvant varier même au sein de la même catégorie de contrat.
Ai-je besoin d'un permis de frontalier pour un poste dans le canton de Bâle ?
Les résidents UE/AELE domiciliés dans la zone frontalière du pays voisin du canton de Bâle peuvent demander un permis G ; l'employeur suisse le dépose auprès de l'office cantonal des migrations après signature du contrat. Les règles de zone frontalière et les délais varient selon le pays voisin et le canton — confirmez les détails auprès de l'office des migrations du canton de Bâle ou avec les RH pendant la candidature.
Comment postuler à ce poste chez Roche ?
Utilisez le bouton « Postuler maintenant » sur cette page — il renvoie directement à l'annonce originale de Roche sur roche.wd3.myworkdayjobs.com, votre candidature arrive donc directement dans le système de suivi des candidatures de l'employeur. Frontaliere Ticino ne collecte ni ne transmet lui-même les candidatures.
