Remote Start-Up Manager, Clinical Trials

Embedded Shishya

United States

Remote

USD 64,000 - 93,000

Full time

14 days+
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Benefits offered by this job

Permanent full-time position
Flexible schedule
Vacation
Home-based position
Ongoing learning and development

Job summary

Indero, a global clinical leader in dermatology, seeks a Start-Up Manager for Canada with remote work. You will oversee site activation across multiple countries, lead all start-up activities, ensure regulatory compliance, and collaborate with cross-functional teams to meet study timelines and client expectations.

Responsibilities include end-to-end start-up, site selection, regulatory submissions, budgeting, multi-country coordination, and client-facing communication.

Qualifications

  • Bachelor’s in Life Sciences, Nursing or related field.
  • Master’s degree preferred.
  • 3+ years in clinical trial start-up with leadership experience.

Responsibilities

  • Manage end-to-end study start-up including site selection, regulatory submissions, contracting and budgeting.
  • Define start-up strategy and timelines with PM and cross-functional leads.
  • Prepare and maintain a site activation plan across countries and sites.
  • Identify issues impacting delivery and propose solutions.
  • Monitor progress against timelines and address delays or risks.
  • Oversee each step of the start-up process to meet activation goals.
  • Serve as primary liaison among functions during start-up for effective collaboration.
  • Track and report start-up performance metrics for transparency.
  • Lead client-facing calls and act as main contact for start-up with Sponsors.

Skills

Project management
Communication
Leadership
Problem solving

Education

Bachelor’s degree in Life Sciences/Nursing
Master’s degree preferred

Job description

Indero, a global clinical leader in dermatology, seeks a Start-Up Manager for Canada with remote work. You will oversee site activation across multiple countries, lead all start-up activities, ensure regulatory compliance, and collaborate with cross-functional teams to meet study timelines and client expectations.

Responsibilities include end-to-end start-up, site selection, regulatory submissions, budgeting, multi-country coordination, and client-facing communication.

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