• Job Title
  • Scope
  • {{content-2}}
  • Clinical Manager
  • 1. Assisting in the management and coordination of clinical trials, including but not limited to daily operational tasks, addressing trial needs, and ensuring smooth execution. The role also involves overseeing clinical trial activities, including site selection, PI and CRO coordination, vendors management,
    regulatory compliance, safety reporting, trial progress management, data
    integrity, and financial oversight.

    2. Supporting cross-functional teams, including but not limited to marketing, business development, and R&D, as needed to meet organizational objectives.

    3. Contributing to the preparation, review, and organization of clinical trial documentation, including but not limited to study protocols, study manuals and plans, patient-facing materials, study reports, regulatory submissions, and trial-related correspondence, ensuring that trials are conducted in compliance with applicable regulations and organizational standards.

    4. Assisting in the development and implementation of strategies to improve trial execution and efficiency.

    5. Supporting business development initiatives, including identifying new trial opportunities, assisting in proposal submissions, and helping to expand the company’s clinical trial portfolio.

    6. Completing tasks and assignments as directed by the supervisor, including but not limited to ad-hoc project support and R&D-related tasks.
  • {{content-2}}
  • Job Title
  • Scope
  • {{content-2}}
  • Job Title
  • Clinical Manager
  • {{content-2}}
  • Scope
  • 1. Assisting in the management and coordination of clinical trials, including but not limited to daily operational tasks, addressing trial needs, and ensuring smooth execution. The role also involves overseeing clinical trial activities, including site selection, PI and CRO coordination, vendors management,
    regulatory compliance, safety reporting, trial progress management, data
    integrity, and financial oversight.

    2. Supporting cross-functional teams, including but not limited to marketing, business development, and R&D, as needed to meet organizational objectives.

    3. Contributing to the preparation, review, and organization of clinical trial documentation, including but not limited to study protocols, study manuals and plans, patient-facing materials, study reports, regulatory submissions, and trial-related correspondence, ensuring that trials are conducted in compliance with applicable regulations and organizational standards.

    4. Assisting in the development and implementation of strategies to improve trial execution and efficiency.

    5. Supporting business development initiatives, including identifying new trial opportunities, assisting in proposal submissions, and helping to expand the company’s clinical trial portfolio.

    6. Completing tasks and assignments as directed by the supervisor, including but not limited to ad-hoc project support and R&D-related tasks.
  • {{content-2}}
  • Job Title
  • Clinical Manager
  • {{content-2}}