Clinical Trial Project Coordinator

hace 2 días

Barcelona, Barcelona, España Innovaderm Research A tiempo completo
About the Role

The Associate Project Manager is a key member of our clinical trial project management team. This role involves working closely with the Project Manager and functional team members to ensure the successful delivery of clinical trials.

Key responsibilities include tracking study budgets, project scope, and timelines, as well as communicating project information to stakeholders. The Associate Project Manager will also be responsible for designing templates, creating presentations, reviewing and editing project deliverables, and maintaining the project information repository.

This role is perfect for individuals who are looking for a challenging and rewarding career opportunity in clinical research. If you have a strong background in project management and are looking to take your career to the next level, this could be the ideal role for you.

Responsibilities
  • Communicate project information to stakeholders, including the Sponsor, vendors, and internal team members
  • Track and manage established plans to ensure all deliverables and milestones are met
  • Coordinate tasks and deadlines between different departments involved in the project
  • Contribute to the management of needs and expectations of the Sponsor and other internal and external project stakeholders
  • Contribute to adequate training of team members on the project
  • Plan the activities and resources required for the project
  • Manage the quality of assigned work
  • Assist with providing project status updates
  • Analyze discrepancies between planned and actual results and participate in the development and implementation of corrective actions
  • Assist with enforcing effective change control and risk management throughout the project
  • Develop and review project operational plans and manuals as applicable
  • Assist with ensuring that study-specific documents and project deliverables meet requirements
  • Participate in the planning and conduct of Investigator's Meeting
  • Support sites and ensure that each site has the necessary material to adequately perform the study
About Innovaderm

Innovaderm is a contract research organization (CRO) specialized in dermatology. We have a solid reputation for the quality of our research and services, and we continue to grow and expand in North America and Europe.

We are committed to providing equitable treatment and equal opportunity to all individuals. As such, we will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.

We only accept applicants who can legally work in Spain.

Requirements
  • Bachelor's degree in a related field of study to clinical research
  • At least 3 years of experience in a similar role, including activities related to management of clinical studies in the pharmaceutical, biotechnology, and/or CRO industry
  • Excellent knowledge of GCP and ICH standards, FDA and Canadian regulations
  • Excellent knowledge of Microsoft Office suite
  • Excellent oral and written skills in English, French is an asset
  • Excellent communication skills
  • Ability to work in a team environment and establish good relationships with colleagues and sponsors
  • Good problem-solving abilities
  • Good organizational skills
  • Strong ability to carry out different projects and work under pressure while meeting timelines
  • Experience managing small to medium projects using a disciplined approach to project management
  • Core Project Management competencies
  • Demonstrated ability to establish and deliver resource-based project plans
  • Excellent people management skills; experience working with and managing teams in a matrix environment

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