Our client is a global pharmaceutical company located near Neuchatel, Switzerland
Focused on research and clinical development of innovative medicines across several therapeutic areas, including oncology, hematology and immunology.
Flexible working: 50% on-site, 50% home-based.
The successful candidate will be involved in leading a complex combination therapy trial and responsibilities will include:
Assist the Clinical Research Scientist team to interface with project team members including Clinical Research Physician, Clinical Operations, Data Management, Statistics, Drug Safety, Regulatory and Project Management.
Review and query of hematology/oncology data including safety, primary efficacy variables, and laboratory data.
Assist with protocol preparation (writing, reviewing, amending and cross-functional facilitation as appropriate).
Assist with study start-up activities and database build
Participate or lead in Scientific meetings (i.e. Ad-Board, Steering Committee, Data Monitoring Committee)
Potentially assume study lead responsibilities, manage study, work independently
Multi-tasking, i.e. working on multiple studies and/or multiple deliverables
Experience and Education
Advanced Degree in Life Sciences (e.g., nursing, pharmacy or related medical field)
Minimum 5 years’ experience as a clinical scientist or equivalent
Clinical development experience in oncology/hematology
Excellent written and verbal communication skills and interpersonal skills.
Knowledge of clinical trial design, basic statistics, and data review tools
Experience in data review and medical monitoring of data
Proficient at data interpretation
Experience in protocol development, study report preparation, Investigator Brochure preparation, regulatory submissions
Full understanding of GCP and ICH Guidelines
Ability to assimilate technical and scientific information quickly
Proficient in Microsoft Office (Word, Excel, PowerPoint; Microsoft project a plus), J-Review, EDC (Rave)
Demonstrated ability to work as part of a team
***This position has now been filled, please contact firstname.lastname@example.org to be informed of future similar positions***