Remote Clinical Project Manager – GI Trials

Alimentiv; Templetown; A distancia; GBP 72.000 - 119.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Education Reimbursement program for FT

Monthly Cell Phone and Remote Work0Al

Office setup allowance

Working while visiting program

Flexible Summer Hours

Employee referral incentive

Alimentiv Trust after 1 year

Alimentorship mentorship program

Descripción de la vacante

Alimentiv, a global CRO focused on GI therapies, is seeking a Clinical Project Manager for home-based work with occasional travel. You will oversee planning, execution, and delivery of clinical research projects, coordinating cross-functional teams and ensuring regulatory compliance.

The ideal candidate has 1–3 years of project management experience in clinical studies, strong communication, and organizational skills, with fluency in English.

Formación

• Bachelor's degree in Health Sciences or related field.
• 1–3 years of clinical study management experience.
• Knowledge of regulatory requirements and study documentation practices.
• Excellent project management and organizational skills.
• Strong written and verbal communication skills.

Responsabilidades

• Lead planning, execution, monitoring, and completion of clinical research projects.
• Coordinate cross-functional teams to ensure regulatory compliance and quality standards.
• Oversee operations, budgets, regulatory requirements, and patient safety throughout the project life cycle.
• Manage essential study documents, data, equipment, and tools (protocols, SOPs, ICFs, CRFs).
• Serve as primary contact for sponsors, manage expectations, and maintain communication.
• Organize project meetings and provide regular progress reports to stakeholders.

Conocimientos

Communication

Organizational skills

Problem-solving

Team coordination

Educación

Bachelor's degree in Health Sciences/Clinical Research

Descripción del empleo

Alimentiv, a global CRO focused on GI therapies, is seeking a Clinical Project Manager for home-based work with occasional travel. You will oversee planning, execution, and delivery of clinical research projects, coordinating cross-functional teams and ensuring regulatory compliance.

The ideal candidate has 1–3 years of project management experience in clinical studies, strong communication, and organizational skills, with fluency in English.