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Senior Clinical Scientist - Oncology (Lymphoma) (EN)

[11749]
Clinical Development, Clinical Scientist, Oncology

Job title: Senior Clinical Scientist - Oncology (Lymphoma) Industry: Pharma Skills: Clinical Development,Clinical Scientist,Oncology Start of project: 01.08.2022 Duration of the project : 12 months' Location: Switzerland - Hybrid 50% onsite  Tasks: ·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 data base build ·Participate or lead in Scientific meetings (ie 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 Qualifications: ·Minimum 6 yrs. experience in oncology/hematology clinical development ·Excellent written and verbal communication skills and interpersonal skills. ·Knowledge of clinical trial design, basic statistics, and data review tools ·Proficient at data interpretation ·Experienced at cleaning both safety and efficacy data (not just safety) ·Capable of leading a complex combination therapy trial with little supervision ·Experience in protocol development, study report preparation, Investigator Brochure preparation, regulatory submissions ·Full understanding GCP and ICH Guidelines ·Phase 1 expereince is a plus  ·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) ·Demonstrated ability to work as part of a team ·Hematology experience (plus). Protocol authoring (preferred). Data review and medical monitoring of data (required). ·Advanced Degree in Life Sciences (e.g  pharmacy or related medical field), minimum 5 years’ experience in clinical research development or equivalent

Job title: Senior Clinical Scientist - Oncology (Lymphoma)
Industry: Pharma
Skills: Clinical Development,Clinical Scientist,Oncology
Start of project: 01.08.2022
Duration of the project : 12 months'
Location: Switzerland - Hybrid 50% onsite 

Tasks:
  • 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 data base build
  • Participate or lead in Scientific meetings (ie 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

Qualifications:


  • Minimum 6 yrs. experience in oncology/hematology clinical development
  • Excellent written and verbal communication skills and interpersonal skills.
  • Knowledge of clinical trial design, basic statistics, and data review tools
  • Proficient at data interpretation
  • Experienced at cleaning both safety and efficacy data (not just safety)

  • Capable of leading a complex combination therapy trial with little supervision

  • Experience in protocol development, study report preparation, Investigator Brochure preparation, regulatory submissions
  • Full understanding GCP and ICH Guidelines
  • Phase 1 expereince is a plus 
  • 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)
  • Demonstrated ability to work as part of a team

  • Hematology experience (plus). Protocol authoring (preferred). Data review and medical monitoring of data (required).

  • Advanced Degree in Life Sciences (e.g  pharmacy or related medical field), minimum 5 years’ experience in clinical research development or equivalent

map Switzerland date_range 01.08.2022 update Temporary
Direct contact

Moritz Janssen

Recruitment Consultant
mail m.janssen@aristo-group.ch
phone +41 44 274 39 00


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