Clinical Development Lead — Idorsia Pharmaceuticals
- Location
- Allschwil
- Contract
- full-time
- Posted
- Yesterday
Role overview
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.
Main responsibilities
- 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.
What the company offers
- Serve as a core member of the Safety Management Team and contribute to the assessment and communication of the compound’s benefit-risk profile.
Additional 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
Notes and original content
- 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
Questions about this listing
What salary does Idorsia Pharmaceuticals offer for this role?
Idorsia Pharmaceuticals lists CHF 99'500 - 169'500 gross per year for this position in Allschwil. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Idorsia Pharmaceuticals offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Idorsia Pharmaceuticals during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Basel?
EU/EFTA residents living in the border zone of the country adjoining Canton Basel can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Basel's cantonal migration office or with HR during the application.
How do I apply for this position at Idorsia Pharmaceuticals?
Use the "Apply now" button on this page — it links directly to Idorsia Pharmaceuticals's original listing at careers.idorsia.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
