Associate Director – Clinical Project Management

Jobtailor

Lisboa

Presencial

EUR 60 000 - 90 000

Tempo integral

14 dias+

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Resumo da oferta

Jobtailor is seeking an experienced Clinical Project Manager in Lisbon to lead operational execution of studies and programs, collaborate on integrated study plans, and act as the main liaison with customers. You will monitor progress, report proactively to stakeholders, and mentor junior staff.

The role requires a decade in clinical research with six years in project management, strong communication, and solid MS Office skills. Knowledge of ICH GCP and local regulations is essential.

Qualificações

  • Requires 10 years clinical research experience including 6 years of project management experience
  • Knowledge of clinical trials and regulatory requirements including ICH GCP and local laws
  • Strong written and verbal communication skills
  • Strong problem solving skills
  • Planning, time management and prioritization skills
  • Good software and computer skills, including MS Office applications

Responsabilidades

  • Manage and support the operational elements and execution of studies and/or programs
  • Develop and/or support on the preparation of integrated study management plans in collaboration with the core project team
  • Serve as primary project oversight and/or contact with customers
  • Monitor progress against contract and prepare/present project information proactively to all stakeholders
  • Coach and/or mentor junior team members
  • Achieve project quality by identifying and proactively managing quality risks and issues

Conhecimentos

Project management
Clinical research
Communication skills
Problem solving
Planning
Time management
Prioritization

Formação académica

Bachelor's Degree Life sciences or related field

Ferramentas

MS Office Applications

Descrição da oferta de emprego

  • Manage and support the operational elements and execution of studies and/or programs
  • Develop and/or support on the preparation of integrated study management plans in collaboration with the core project team
  • Serve as primary project oversight and/or contact with customers
  • Monitor progress against contract and prepare/present project information proactively to all stakeholders
  • Coach and/or mentor junior team members
  • Achieve project quality by identifying and proactively managing quality risks and issues
Requirements
  • Bachelor's Degree Life sciences or related field
  • Requires 10 years clinical research experience including 6 years of project management experience
  • Knowledge of clinical trials - Knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines
  • Strong written and verbal communication skills
  • Strong problem solving skills
  • Planning, time management and prioritization skills
  • Good software and computer skills, including MS Office applications
Core Competencies

Demonstrates extensive experience in clinical research project management, including the development of integrated study management plans and proactive stakeholder communication. Proficient in identifying quality risks and mentoring junior team members to achieve project objectives.

Highest-signal resume keywords
  • Clinical Research Experience
  • Project Management Experience
  • Knowledge of Clinical Trials
  • ICH GCP Compliance
  • Strong Communication Skills
ATS Optimization Keywords
Hard Skills
  • Clinical Research
  • Project Management
  • Study Management Plans
  • Quality Risk Management
  • Regulatory Requirements
Soft Skills
  • Problem Solving
  • Planning
  • Time Management
  • Prioritization
  • Coaching
Industry Keywords
  • Clinical Trials
  • Regulatory Compliance
  • Local Laws
  • Research Guidelines
Tools & Technologies
  • MS Office Applications
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