Clinical Trial Scientist

Location & Contract

Allschwil, Switzerland. Contract duration: 2 years.

• 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.

• Relevant Swiss working/residency permit and/or Swiss/EU‑Citizenship required.
• PhD, Pharm
  
  D, 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.