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 recruitment@consultantsinscience.com for more information or to apply