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Senior Clinical Research Scientist - Hematology/oncology

Consultants in Science Sàrl
  • Date de publication :

    06 janvier 2024
  • Taux d'activité :

    100%
  • Type de contrat :

    Durée indéterminée
  • Lieu de travail :Neuchatel

Senior Clinical Research Scientist - Hematology/oncology

Aug 5, 20221 min read

Updated: May 5, 2023

The Company

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 Role

The successfulcandidate 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

Detail-oriented, well-organized

Ability to assimilate technical and scientific information quickly

Proficient in Microsoft Office (Word, Excel, PowerPoint; Microsoft project a plus), J-Review, EDC (Rave)

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