Clinical Development Lead — Idorsia Pharmaceuticals
- Ort
- Allschwil
- Vertrag
- full-time
- Veröffentlicht
- Gestern
Rollenüberblick
The purpose of Idorsia is to challenge accepted medical paradigms, answering the questions that matter most.
To achieve this, we will discover, develop, and commercialize transformative medicines – either with in-house capabilities or together with partners – and evolve Idorsia into a leading biopharmaceutical company, with a strong scientific core.
Are you an experienced clinical development professional eager to take scientific ownership of a clinical program and help shape the future of a differentiated therapy?
- The purpose of Idorsia is to challenge accepted medical paradigms, answering the questions that matter most.
- To achieve this, we will discover, develop, and commercialize transformative medicines – either with in-house capabilities or together with partners – and evolve Idorsia into a leading biopharmaceutical company, with a strong scientific core.
- Key Responsibilities
- The Clinical Development Lead is the clinical and scientific expert responsible for leading the delivery of clinical program objectives for an assigned compound, in line with Company strategy and agreed development plans. Main responsibilities include:
- Serve as a core member of the Safety Management Team and contribute to the assessment and communication of the compound’s benefit-risk profile.
Hauptaufgaben
- Key Responsibilities
- The Clinical Development Lead is the clinical and scientific expert responsible for leading the delivery of clinical program objectives for an assigned compound, in line with Company strategy and agreed development plans. Main responsibilities include:
- Lead the multidisciplinary Clinical Team at development-program level, providing scientific direction, strategic alignment and accountability across the program.
- Shape innovative clinical development strategies that maximize the compound's value throughout its lifecycle, integrating emerging scientific evidence and evolving standard of care into development plans.
- Lead the scientific development and delivery of clinical sections of trial- and program-level regulatory documents, including Investigator’s Brochures, briefing books, safety updates, submission dossiers and responses to Health Authorities.
- Provide thought leadership in clinical trial design and execution in close partnership with key functions, ensuring scientific quality, clear prioritisation and timely delivery.
- Provide ongoing clinical and scientific review, interpretation and communication of clinical trial data to inform program strategy and development decisions.
- Support the preparation of safety-related documents, including Periodic Safety Update Reports, Drug Safety Update Reports and other safety documentation, in collaboration with the Project Physician and Drug Safety Physician.
- Maintain a strong understanding of the therapeutic area, competitive landscape, relevant mechanisms of action and evolving standards of care.
- Lead clinical contributions to scientific communications, including study abstracts, posters, oral presentations and manuscripts.
Was das Unternehmen bietet
- Serve as a core member of the Safety Management Team and contribute to the assessment and communication of the compound’s benefit-risk profile.
Weitere Details
- The Clinical Development Lead is the clinical and scientific expert responsible for leading the delivery of clinical program objectives for an assigned compound, in line with Company strategy and agreed development plans. Main responsibilities include:
- Champion the clinical perspective in cross-functional discussions and support the continuous evolution of the clinical development strategy. Candidate Requirements
Notizen und Originalinhalt
- The Clinical Development Lead is the clinical and scientific expert responsible for leading the delivery of clinical program objectives for an assigned compound, in line with Company strategy and agreed development plans.
- Main responsibilities include:
- Champion the clinical perspective in cross-functional discussions and support the continuous evolution of the clinical development strategy.
- Candidate Requirements
Fragen zu dieser Stellenanzeige
Welches Gehalt bietet Idorsia Pharmaceuticals für diese Stelle?
Idorsia Pharmaceuticals gibt CHF 99'500 - 169'500 brutto pro Jahr für diese Position in Allschwil 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 Idorsia Pharmaceuticals?
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 Idorsia Pharmaceuticals, 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 Idorsia Pharmaceuticals?
Nutzen Sie die Schaltfläche "Jetzt bewerben" auf dieser Seite — sie führt direkt zum Original-Inserat von Idorsia Pharmaceuticals unter careers.idorsia.com, sodass Ihre Bewerbung direkt im Bewerbermanagementsystem des Arbeitgebers landet. Frontaliere Ticino sammelt oder leitet keine Bewerbungen selbst weiter.
