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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