Clinical Project Manager (Permanent)

Crovelis; Madrid; Presencial; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A clinical research company is seeking an experienced Clinical Project Manager to oversee all phases of clinical projects in Madrid. The ideal candidate will have a university degree in Science, Pharmacy, or Nursing and a minimum of 4-5 years in clinical project management. Responsibilities include coordinating clinical studies, ensuring compliance with regulations, and leading the operational team. Proficiency in English is mandatory. This role offers the chance to work with a multidisciplinary team dedicated to excellence in health and pharmaceutical development.

Formación

• Minimum 4-5 years in clinical project management.
• Proven experience as a Clinical Project Manager in clinical studies.
• Intermediate to advanced spoken and written English (mandatory).

Responsabilidades

• Oversee and coordinate all phases of the clinical project.
• Manage planning, development, and execution of clinical studies.
• Coordinate clinical monitoring with team members.
• Lead adverse event management ensuring compliance.
• Facilitate onboarding and continuous training of the team.

Conocimientos

Clinical project management

Communication

Leadership

Regulatory compliance

Project coordination

Educación

University degree in Science, Pharmacy, Nursing, or related fields

Descripción del empleo

Clinical Project Manager (CPM)

Experience

Minimum 4-5 years in clinical project management

Overview

Crovelis is a company committed to excellence in clinical research, specializing in comprehensive project management that drives innovation in health and pharmaceutical development. You will be part of a highly professional multidisciplinary team where each project represents an opportunity to grow and make a difference in the clinical field.

Responsibilities

• Oversee and coordinate all phases of the clinical project, ensuring compliance with deadlines, budgets, and quality standards.
• Manage the planning, development, and execution of clinical studies, acting as the main project lead.
• Coordinate clinical monitoring, ensuring proper communication and support to CRAs, CTAs, and other team members.
• Organize and facilitate key project meetings including kick-offs, follow-ups, investigator meetings, and vendor meetings.
• Prepare, control, and ensure timely delivery of regular study progress reports to internal and external stakeholders.
• Lead adverse event management and ensure compliance with regulatory and safety requirements.
• Collaborate closely with the Quality Assurance (QA) department during internal and external audits, overseeing the implementation of corrective action plans when needed.
• Facilitate onboarding and continuous training of the operational team to ensure adherence to best practices.
• Coordinate study close-out and final archiving in compliance with regulatory and company standards.
• Act as a key communication link among multidisciplinary departments including Pharmacovigilance, Data Management, Biostatistics, Regulatory Affairs, Supply Chain, and Compliance, ensuring alignment and collaboration across all project-related areas.
• Manage complex clinical projects with rigor, ensuring quality and regulatory compliance at all stages, while providing leadership and strategic vision to achieve study objectives.

Qualifications

• University degree in Science, Pharmacy, Nursing, or related fields.
• Proven experience of at least 4-5 years as a Clinical Project Manager in clinical studies.
• Intermediate to advanced spoken and written English (mandatory).

Additional Information

One or two interviews, either virtual or in-person.