Remote Clinical Project Lead, GI Trials

Alimentiv

Rowley

A distancia

GBP 72.000 - 119.000

Jornada completa

14 días+

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

Supera los filtros ATS

Ventajas ofrecidas por este puesto de trabajo

Education reimbursement
Remote work allowance
Office setup allowance
4 weeks visiting program
Flexible Summer Hours
Referral incentive
Alimentiv Trust after 1 year
Mentorship program

Descripción de la vacante

Alimentiv is seeking a motivated Clinical Project Manager to oversee planning, delivery, and regulatory compliance of clinical research projects. This home-based role involves coordinating cross-functional teams, managing timelines and budgets, and maintaining sponsor relationships.

Travel is occasional, and strong communication and organizational skills are essential. The ideal candidate has 1–3 years in clinical study management, a solid understanding of study documentation, and fluency in

Formación

  • Bachelor's degree in Health Sciences, Clinical Research, or related field.
  • 1–3 years of clinical study management experience.
  • Strong knowledge of clinical research processes and regulatory requirements.
  • Excellent project management and organizational skills.
  • Effective written and verbal communication with sponsors and teams.
  • Ability to collaborate across cross-functional teams.
  • Detail-oriented with commitment to compliance and quality.
  • Fluent English and ability to work remotely with travel.

Responsabilidades

  • Lead planning, execution, monitoring, and completion of assigned clinical research projects.
  • Coordinate cross-functional project teams to ensure compliance with regulations, guidelines, policies, and quality standards.
  • Oversee project operations, budgets, regulatory requirements, and patient safety.
  • Manage development, maintenance, and disposal of essential clinical study documents and data.
  • Assign, track, and oversee site monitoring, data collection, adverse event management, statistics, and reporting.
  • Serve as primary contact for sponsors and clients, proactively managing expectations and issues.
  • Organize and facilitate project meetings, provide investigator updates, and progress reports.
  • Support site and patient recruitment strategies and training initiatives.
  • Participate in regulatory submissions, audits, vendor selection, and related activities.

Conocimientos

Clinical project management
Regulatory compliance
Budgeting
Communication
Cross-functional coordination
Attention to detail
Remote work

Educación

Bachelor's degree in Health Sciences/Clinical Research

Descripción del empleo

Alimentiv is seeking a motivated Clinical Project Manager to oversee planning, delivery, and regulatory compliance of clinical research projects. This home-based role involves coordinating cross-functional teams, managing timelines and budgets, and maintaining sponsor relationships.

Travel is occasional, and strong communication and organizational skills are essential. The ideal candidate has 1–3 years in clinical study management, a solid understanding of study documentation, and fluency in

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