Clinical Scientist

CHF85 - CHF90 per hour
  1. Interim/Contract
Bern
  1. Clinical Development, Clinical Scientist
Posted: 15/05/2020
BBBH14033

This vacancy has now expired. Please see similar roles below...

Hobson Prior are currently working with a world-wide biopharma organisation focused on improving the lives of patients globally through pioneering medicines. Our client is seeking a Clinical Scientist to join them on a permanent basis in Switzerland.


Job Responsibilities:

  • Accountable to review 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.
  • You will 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.
  • Partake and/or Lead team meetings as required.

Key Skills:

  • Ability to function independently in data review to identify discrepancies in clinical trial data and to write queries from a medical perspective.
  • Ability to communicate medical or clinical information to a physician.
  • Ability to understand clinical trial publications; understanding of disease.

Requirements:

  • Experience working on clinical trials as a Clinical Research Scientist from a sponsor's perspective.
  • At least two years of direct Haematology/Oncology experience in a Clinical Research and Development capacity.
  • Must have experience performing data review in Haematology/Oncology indications.
  • Experience in performing review of clinical trial data in order to identify trends in safety or efficacy data.
  • 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.
  • Some experience in medical writing such as authoring or co-authoring documents such as protocol, clinical study report, investigators brochure, patient narrative
  • Degree in life sciences.

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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