Senior Clinical Research Scientist - contractor Neuchatel

Our client is a global biopharmaceutical company with pipelines in oncology and hematology.

The company is looking for a contractor for the position of Senior Clinical Research Scientist to work at their site in the Neuchatel area, Switzerland. The contract length is 12 months.

Core job responsibilities:

  • Assist the Clinical Research Scientist team in the extrapolation and review of study data from the investigator sites.

  • Responsible for interacting with study sites to review, extrapolate, collect, study data, including, but not limited to, patient diagnosis, treatment plans/regimen, adverse event documentation and reporting, clinical response, and long-term follow-up.

  • May assist with designing data capture worksheets for investigator sites

  • Reviews and verifies source documentation to determine accuracy and completeness of the information and communicate discrepancies to the clinical team for action resolution.

  • Adhere to standard operating procedures, protocols, and study-specific guidelines

  • Provide updates to clinical team as appropriate

  • Participate in job-related training and ad-hoc meetings

Knowledge & Skills Required:

  • Advanced Degree (preferred) or bachelor's degree in Life Science: nursing (preferred), pharmacy or related medical field

  • Oncology Registered Nursing certification (preferred) or equivalent certification/licensure from an appropriately accredited institution

  • Minimum 5 years' experience in clinical research development or equivalent

  • Oncology experience (required). Minimum 5 yrs. experience in an oncology clinical research or hospital setting.

  • Hematology experience (preferred)

  • Must have the ability to establish and maintain effective working relationships with the study team and Principal Investigators /site coordinators.

  • Strong professional interpersonal skills

  • Excellent written and verbal communication skills

  • Knowledge of clinical trial design

  • Proficient at data interpretation

  • Understanding GCP and ICH Guidelines

  • Detail-oriented, well-organized

  • Ability to assimilate technical and scientific information quickly

  • Proficient in Microsoft Office (Word, Excel, PowerPoint; Microsoft project a plus), JReview (plus), EDC system (plus)

  • Demonstrated ability to work as part of a team

  • Time Management

Please contact for more information or to apply