Location & Contract
Allschwil, Switzerland. Contract duration: 2 years.
Responsibilities
* Act as a core member of the Clinical Trial Team (CTT) and collaborate closely with the Clinical Trial Physician.
* Scientific planning, conduct, data review, and reporting of Phase II and III clinical trials.
* Authoring and co-authoring of key clinical trial documents, including protocols, ICFs, study committee charters, guidelines, and CSR.
* Collaboration with other teams to develop, refine, or finalize SAPs, CRFs, and monitoring guidelines to ensure full compliance.
* Data review and medical monitoring during trial conduct.
* Coordination and management of study committees.
* Scientific input to IRB/EC and Health Authority responses.
* Participation in scientific discussions with external experts.
* Training of internal stakeholders on the scientific aspects of the trial.
Qualifications
* Relevant Swiss working/residency permit and/or Swiss/EU‑Citizenship required.
* PhD, PharmD, MSc, or equivalent degree in life or health sciences.
* At least 2 years of experience in clinical development (CRO or pharmaceutical company).
* Experience with Phase II and III clinical trials.
* Strong analytical, organizational, and problem‑solving skills, and a proactive, independent approach.
* Ability to prioritize and deliver under tight timelines.
* Excellent communication and stakeholder management skills.
* Global mindset and willingness to travel occasionally.
* Fluency in English.
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