Remote Clinical Project Manager – GI Trials

Alimentiv

Austin (TX)

A distancia

USD 85.000 - 120.000

Jornada completa

Hace 7 días
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Ventajas ofrecidas por este puesto de trabajo

Education reimbursement
Remote work allowance
Office setup allowance
Flexible summer hours
Alimentiv Trust
Performance incentives
STIP

Descripción de la vacante

Alimentiv, a global CRO, is seeking a Clinical Project Manager to oversee planning, execution, and delivery of clinical research projects. You will coordinate cross-functional teams, manage timelines, ensure regulatory compliance, and maintain sponsor relationships from a home-based setup with occasional travel.

The ideal candidate has 1–3 years in clinical study management, strong communication and organisational skills, and a collaborative approach to achieving project objectives.

Formación

  • Bachelor's degree in health sciences, clinical research or related field.
  • 1–3 years of experience in clinical study management or project coordination.
  • Solid understanding of regulatory requirements and study documentation practices.

Responsabilidades

  • Lead planning, execution, monitoring and completion of clinical projects.
  • Coordinate cross-functional teams to ensure regulatory compliance and quality standards.
  • Oversee budgets, regulatory requirements and patient safety throughout the life cycle.
  • Manage study documents, data, CRFs and other essential trial artifacts.
  • Communicate updates and progress to sponsors and stakeholders.

Conocimientos

Project management
Regulatory knowledge
Cross-functional leadership
Communication

Educación

Bachelor's in Health Sciences

Herramientas

CTMS

Descripción del empleo

Alimentiv, a global CRO, is seeking a Clinical Project Manager to oversee planning, execution, and delivery of clinical research projects. You will coordinate cross-functional teams, manage timelines, ensure regulatory compliance, and maintain sponsor relationships from a home-based setup with occasional travel.

The ideal candidate has 1–3 years in clinical study management, strong communication and organisational skills, and a collaborative approach to achieving project objectives.

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