Reference number
Start date
My duties
  • Developing a sound understanding of the science and medicine relating to a the therapeutic area
  • Developing a sound understanding of the complexity of global clinical development with a particular attention to methodological and ethical aspects of development, in the assigned therapeutic area
  • Performing literature reviews, and write position papers as necessary
  • Contribute to writing of protocol and core informed consent form (CICF), including amendments input into the Clinical Study Report (CSR)
  • Medical training of the Clinical Trial Team (CTT) members and/or my clients staff
  • Medical oversight of the study (including safety, quality and performance of the trial)
  • Clinical Trial results interpretation
  • Involved in the organization and management of the following external activities: Contacts with external experts, steering committees (SC), independent data monitoring committees (IDMC), other study or project committees
  • Answering to trial-related EC/IRB and HA questions
  • Ensuring that the Case Report Form is designed to allow careful and comprehensive collection of data
My qualifications
  • MD and profound experience in clinical research in a pharmaceutical or biotech company or equivalent in Academia
  • Clinical research or clinical experience in the indication relevant to the clinical project is preferred
  • Good knowledge of drug development and clinical trial process based on previous experience
  • Good knowledge of regulatory requirements/ICH guidelines
  • Good organizational skills, able to work as part of a team and independently
  • Good communication skills
  • Detailed oriented
  • Fluency in English
My benefits
  • Flexible work hours
  • Being part of a great team that works on interesting indications
  • Immediate start in contract possible
  • This opportunity is open for people who want to make a switch to the private sector
My assignment
    The client is an innovative Pharma company that is working on new indications and is growing fast. All tasks should be performed in compliance with Good Clinical Practices and the client SOP’s. The CTP is a member of the Clinical Trial Team (CTT). The tasks and activities of the CTP are carried out in close collaboration with the Clinical Trial Scientist (CTS) for the trial related activities and with the Clinical Project Physician (CPP) and Clinical Project Scientist (CPS) for the project related activities.
Salary details
  • You are able to start in a contract of 12 months with a very interesting salary and benefits
About Hays
With over 15 years of experience in the pharmaceutical industry, 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 professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays

My contact person
Jadie Ann Vallons

Reference number

Phone: +41-61-2250 - 586
E-Mail: jadie.vallons@hays.ch