Clinical Research Scientist – Spring Professional – La Chaux-de-Fonds, NE

We are recruiting on an urgent mandate an experienced Clinical Research Scientist in the field of Cellular Therapy in Hematology.
You have more than 3 years experience as a Clinical Research Scientist and are looking for a new experience, feel free to apply with us.
Only profiles with the right experience in clinical research in the induistry will be considered.

Responsibilities

  • Review of clinical data within eCRF system, patient profiles, etc. to issue queries and clean data from clinical perspective
  • Conduct review of ongoing summary data including: safety, primary efficacy variables, and laboratory data.
  • Assist the Clinical Research Physician to interface with project team members including: Clinical Operations, Data Management, Statistics, Drug Safety, Regulatory and Project Management.
  • Prepare or assist with preparation of key documents e.g. Investigator Brochures, regulatory submission documents, internal or external presentations, etc.
  • Protocol preparation (writing, reviewing, amending and cross-functional facilitation as appropriate).
  • Clinical study report preparation
  • Review literature and prepare summary documents for inclusion in IB, protocols regulatory submission documents, etc.
  • Participate and/or Lead team meetings as required


Profile

  • Degree in Life Science: Minimum Master of Science in Life Science
  • Must have experience working on clinical trials as a Clinical Research Scientist from a sponsor’s perspective.
  • Must have: at least two years of direct HEMATOLOGY/ONCOLOGY experience in a Clinical Research and Development, Clinical Science capacity
  • Must have experience performing data review in HEMATOLOGY/ONCOLOGY indications
  • Experience in performing review of clinical trial data in order to identify trends in safety or efficacy data.
  • Ability to function independently in data review to identify discrepancies in clinical trial data and to write queries from a medical perspective.
  • Familiarity with Medidata, RAVE, J-review or other clinical databases or other data review tools (patient profiles, listings) would demonstrate the candidate’s familiarity with the scope of work.
  • Experience in medical writing such as authoring or co-authoring documents such as protocol, clinical study report, investigators brochure, patient narrative
  • Ability to communicate medical or clinical information to a physician.
  • Ability to understand clinical trial publications; understanding of disease


Contact

Spring Professional Life Science: +41 58 233 40 20

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