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Clinical Scientist (EN)

[11745]
Clinical Scientist, Clinical R&D, Clinical Data Management

Job title: Clinical Scientist Industry: Pharma Skills: Clinical Scientist,Clinical R&D,Clinical Data Management Start of project: 01.08.2022 Duration of the project : 6 months Location: Switzerland - Hybrid, 1 day onsite  Position Summary/Objectives: The Clinical Scientist function provides scientific expertise necessary to design and deliver clinical studies and programs. ·Will be responsible for design and execution of assigned clinical trial activities and work closely with clinical team members within the assigned project to execute activities associated with the conduct ·May serve as Clinical Trial Lead for one or more trials ·May lead or support trial level activities for one or more trials with the necessary supervisio ·May co-lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members Position Responsibilities: ·Collaborate and liaise with external partners (e.g., KOLs) ·Seek out and enact best practices with instruction ·Provide regular and timely updates to manager/management as requested ·Develop Protocol and ICF documents / amendments and present these to governance committee and development team meetings as required ·Conduct literature review ·Submit clinical documents to TMF ·Develop site and CRA training materials and present these at SIVs and Investigator meetings ·Review clinical narratives ·Monitor clinical data for specific trends ·Develop Data Review Plan in collaboration with Data Management ·Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming ·Submit clinical contributions to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, PSUR, Orphan Annual Reports, HA, EC, IRB responses and contribute to regulatory submission.) Qualifications: ·Basic knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations ·Ability to understand assigned protocol(s) and their requirements ·Basic knowledge skills to support program-specific data review and trend identification ·Intermediate medical writing skills and medical terminology ·Basic planning/project management skills (develop short range plans that are realistic and effective) ·Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred).  Appropriate for new entrance to pharma (post fellowship/ new to industry) ·Intermediate skills in Microsoft Word/Excel/PowerPoint and data review tools (e.g., Pt Profiles, report generating tools) ·Adaptable / flexible (willing and able to adjust to multiple demands and shifting priorities; ability to meet day-to-day challenges with confidence and professionalism) ·Intermediate critical thinking and problem-solving skills ·Basic knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committees ·Basic knowledge of disease area, compound, current clinical landscape ·Detail-oriented with commitment to quality

Job title: Clinical Scientist
Industry: Pharma
Skills: Clinical Scientist,Clinical R&D,Clinical Data Management
Start of project: 01.08.2022
Duration of the project : 6 months
Location: Switzerland - Hybrid, 1 day onsite 


Position Summary/Objectives:

The Clinical Scientist function provides scientific expertise necessary to design and deliver clinical studies and programs.
  • Will be responsible for design and execution of assigned clinical trial activities and work closely with clinical team members within the assigned project to execute activities associated with the conduct
  • May serve as Clinical Trial Lead for one or more trials
  • May lead or support trial level activities for one or more trials with the necessary supervisio
  • May co-lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members

Position Responsibilities:


  • Collaborate and liaise with external partners (e.g., KOLs)
  • Seek out and enact best practices with instruction
  • Provide regular and timely updates to manager/management as requested
  • Develop Protocol and ICF documents / amendments and present these to governance committee and development team meetings as required
  • Conduct literature review
  • Submit clinical documents to TMF
  • Develop site and CRA training materials and present these at SIVs and Investigator meetings
  • Review clinical narratives
  • Monitor clinical data for specific trends
  • Develop Data Review Plan in collaboration with Data Management
  • Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming
  • Submit clinical contributions to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, PSUR, Orphan Annual Reports, HA, EC, IRB responses and contribute to regulatory submission.)


Qualifications:

  • Basic knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations
  • Ability to understand assigned protocol(s) and their requirements
  • Basic knowledge skills to support program-specific data review and trend identification
  • Intermediate medical writing skills and medical terminology
  • Basic planning/project management skills (develop short range plans that are realistic and effective)
  • Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred).  Appropriate for new entrance to pharma (post fellowship/ new to industry)


  • Intermediate skills in Microsoft Word/Excel/PowerPoint and data review tools (e.g., Pt Profiles, report generating tools)

  • Adaptable / flexible (willing and able to adjust to multiple demands and shifting priorities; ability to meet day-to-day challenges with confidence and professionalism)

  • Intermediate critical thinking and problem-solving skills

  • Basic knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committees

  • Basic knowledge of disease area, compound, current clinical landscape

  • Detail-oriented with commitment to quality


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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