Clinical Development Lead — Idorsia Pharmaceuticals
- Località
- Allschwil
- Contratto
- full-time
- Pubblicato
- Ieri
Panoramica
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.
Responsabilità principali
- 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.
Cosa offre l’azienda
- Serve as a core member of the Safety Management Team and contribute to the assessment and communication of the compound’s benefit-risk profile.
Dettagli ulteriori
- 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
Note e contenuto originale
- 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
Domande frequenti su questo annuncio
Che stipendio offre Idorsia Pharmaceuticals per questa posizione?
Idorsia Pharmaceuticals indica CHF 99'500 - 169'500 lordi annui per questo ruolo a Allschwil. Questo è lo stipendio pubblicato nell'annuncio originale (o, quando il datore non specifica una cifra, una stima realistica per ruolo e settore) — il calcolatore di questo sito lo converte nel netto reale una volta applicate imposta da frontaliere e contributi sociali.
È un ruolo a tempo pieno, e che tipo di contratto offre Idorsia Pharmaceuticals?
Questo annuncio è una posizione a tempo pieno. Il tipo di contratto mostrato qui arriva direttamente dall'annuncio originale del datore di lavoro; conferma sempre orario esatto, preavviso e durata del periodo di prova con Idorsia Pharmaceuticals durante il colloquio, perché questi dettagli possono variare anche all'interno della stessa categoria contrattuale.
Serve un permesso da frontaliere per un ruolo nel canton Basilea?
I residenti UE/AELS nella zona di frontiera del paese confinante con il canton Basilea possono richiedere il Permesso G; il datore di lavoro svizzero lo presenta all'ufficio della migrazione di quel canton dopo la firma del contratto. Regole sulla zona di frontiera e tempi di lavorazione variano per paese confinante e canton — verifica i dettagli con l'ufficio della migrazione del canton Basilea o con HR durante il colloquio.
Come mi candido a questa posizione presso Idorsia Pharmaceuticals?
Usa il pulsante "Candidati ora" in questa pagina — rimanda direttamente all'annuncio originale di Idorsia Pharmaceuticals su careers.idorsia.com, quindi la tua candidatura arriva direttamente nel sistema di gestione candidature del datore di lavoro. Frontaliere Ticino non raccoglie né inoltra candidature in proprio.
