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Clinical Trial Manager (m/w/d) (EN)

[14034]
Clinical Trial Management

Job title: Clinical Trial Manager (m/w/d) Industry: Pharma Skills: Clinical Trial Management Start of project: 01.02.2024 Duration of the project : 12 Months Location: Basel, Schweiz Clinical Trial Managers with expertise in one of our priority therapeutic area (Oncology, Cardiovascular/Metabolic, Infectious Disease, CNS and more) are equally welcome to continue to work in their area of expertise or to expand to a new therapeutic area. Responsibilities ·Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations ·Serve as primary Sponsor contact for operational project-specific issues and study deliverables ·Maintain in depth knowledge of protocol, therapeutic area, and indication ·Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided ·Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable ·Develop operational project plans ·Manage risk assessment and execution ·Responsible for management of study vendor ·Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables Qualifications ·Bachelor’s degree in a health or science-related field; Advanced degree in a health or science-related field preferred; ·Experience in Phases 1-4; Phases 2-3 preferred; ·5+ years as a project/clinical trial manager; ·Management of overall project timeline; ·Strong leadership skills.

Job title: Clinical Trial Manager (m/w/d)
Industry: Pharma
Skills: Clinical Trial Management
Start of project: 01.02.2024
Duration of the project : 12 Months
Location: Basel, Schweiz

Clinical Trial Managers with expertise in one of our priority therapeutic area (Oncology, Cardiovascular/Metabolic, Infectious Disease, CNS and more) are equally welcome to continue to work in their area of expertise or to expand to a new therapeutic area.

Responsibilities
  • Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
  • Serve as primary Sponsor contact for operational project-specific issues and study deliverables
  • Maintain in depth knowledge of protocol, therapeutic area, and indication
  • Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
  • Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
  • Develop operational project plans
  • Manage risk assessment and execution
  • Responsible for management of study vendor
  • Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables

Qualifications
  • Bachelor’s degree in a health or science-related field; Advanced degree in a health or science-related field preferred;
  • Experience in Phases 1-4; Phases 2-3 preferred;
  • 5+ years as a project/clinical trial manager;
  • Management of overall project timeline;
  • Strong leadership skills.

map Basel, Schweiz date_range 01.02.2024 update Freelance
Direct contact

Bella Iglesias

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


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