Jobangebot: Clinical/Medical Scientist (m/f/d)

Über uns

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

Aufgaben

• Draft and review key clinical trial and program-level documents in close collaboration with Clinical Operations, Biostatistics, Medical Writing, and CRO partners
  
• Oversee clinical aspects of study start-up, execution, and close-out, working closely with Clinical Operations, Data Management, and CROs
  
• Support medical monitoring of efficacy and safety data, contributing to timely issue identification and resolution
  
• Serve as a direct clinical contact for investigational sites, ensuring smooth trial conduct across start-up, execution, and close-out phases
  
• Own the clinical components of the Data Review Plan and Trial Master File (TMF), ensuring completeness, quality, and inspection readiness
  
• Support analysis, interpretation, and dissemination of clinical trial data, including scientific publications, investigator meetings, and clinical development team operations

Profil

• Bachelor’s degree or advanced degree in a scientific discipline or Medical Degree
  
• Experience in the pharmaceutical industry, including multiple years in Clinical Development, with responsibility for multiple clinical trials
  
• Proven experience working in fully outsourced CRO models and leading multidisciplinary trial teams
  
• Strong medical and scientific expertise relevant to the clinical program, with the ability to build effective partnerships with investigators
  
• Thorough knowledge of GCP, clinical trial design, statistics, regulatory requirements, and the overall clinical development process
  
• Excellent scientific writing and communication skills, with the ability to interpret data, identify trends, and clearly present trial- or program-level results

Wir bieten

• Challenging and varied assignments in a promising and innovative industry
• Longterm project

Ihr Kontakt

Referenznummer
871198/1

Kontakt aufnehmen
Telefon:+41 44 225 50 00
E-Mail: positionen@hays.ch

Anstellungsart
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