Position: Associate

Job type: Contract

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Job content

A new opportunity has arisen for a Clinical Trial Manager for a small R&D company in French speaking part of Switzerland. To join on a temporary position with options to go permanent at the end of the contract. You will be joining a small team at an exciting time with their launch for a global phase III study working within Antibiotics. You will be taking on further responsibilities as a CTM and you will have the opportunity to take on additional Project manager tasks as you report directly to the Head of Clinical operations. This is a hybrid role which offer flexibility to work from home.

Job Responsibilities
  • Study management.
  • Setting up and designing the trials.
  • Regulatory compliance.
  • Follow up and reporting.
  • Clinical trial documentation.
  • Partake in the clinical development plan team.
  • Coordination and supervision.
  • Project analysis.
Skills And Requirements
  • Study management.
  • Trial set up.
  • Regulatory compliance.
  • Clinical trial follow up.
  • Clinical trial documentation.
  • Management skills.
  • Project review.
Experience
  • Minimum 5 years of experience in clinical trial management.
  • CRO oversight experience.
  • Previous experience within data management is preferred.
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Carl Sundell on +41 61 508 70 52.

A Full Job Description Is Available On Request.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#ClinicalServices

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Deadline: 09-06-2024

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