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Clinical Research Scientist

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Providing Flexible Resourcing Solutions

CTC Clinical Trial Consulting, founded in Basel, Switzerland in 1997, is a specialist staffing organisation, providing flexible resourcing solutions to the pharmaceutical industry in Switzerland, with contract and permanent placements in clinical development, data management, statistics, regulatory affairs and medical marketing.

For one of our clients, we are currently looking for a

Clinical Research Scientist

  • Reference Number: 10-09-106-CRS-CRf
  • Type of placement: Permanent
  • Location: Switzerland, Basel

Basic function:

To support the Clinical Research Manager in all aspects of planning, execution and reporting of one or more clinical trial(s) (Phase I through lifecycle management) including operational as well as scientific aspects

Main responsibilities:

  • Ensure all operational trial deliverables are met according to timelines, budget, operational procedures and quality standards
  • Contribute to the development of specific sections of protocols and related study documents (e.g. study tools, guidelines, training materials)
  • Prepare clinical outsourcing specifications and follow-up with Contract Research Organizations (CROs) to ensure adherence to scope of work within timelines and budget
  • Support the Clinical Research Manager in managing the cross-functional Trial Team including interactions with the Operations Department, Drug Supply Management and the local company affiliates
  • Accountable for accuracy of trial information in all trial databases and tracking systems
  • Participate in the ongoing scientific review of clinical trial data during the course of the study and in trial data analysis and reporting
  • Prepare training materials and presentations related to the planning and conduct of the trial
  • Contribute to program level activities (e.g. tracking of brand-related publications, development of clinical sections of regulatory documents like Investigator’s brochures, briefing books, safety updates, IND/NDA submission documents, responses to Health Authorities questions)

Qualifications and experience:

  • Advanced degree or equivalent education/degree in life science/healthcare with at least 2 years experience in clinical research OR
  • Bachelor degree or equivalent education/degree in life science/healthcare with at least 4 years experience in clinical research
  • Fluent in both written and spoken English
  • Demonstrated ability to work in a cross-functional, multicultural and international team
  • Excellent communication, organization and tracking skills
  • Basic knowledge of Good Clinical Practice; good knowledge of scientific principles
  • Knowledge of oncology is preferable
  • Relevant working/residency permit or Swiss/EU-Citizenship

Our offer:

  • Competitive salary and package
  • Wide range of career opportunities in a large pharmaceutical organisation
  • International experience

Should you be interested in the above position and wish to apply, please send your application with your CV, quoting the above reference number, to our recruitment team at recruitment@ctcon.ch

CTC Clinical Trial Consulting, Greifengasse 1, CH 4058 Basel, Switzerland
Tel.: +41 61 695 88 66       Fax: +41 61 695 88 67       www.ctcon.ch       info@ctcon.ch



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