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Associate Project Manager (Germany)

Indero

Deutschland

Remote

EUR 50.000 - 70.000

Vollzeit

Vor 13 Tagen

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Zusammenfassung

Indero is seeking an Associate Project Manager for clinical trial management, responsible for tracking budgets, timelines, and project deliverables. This home-based position in Germany requires strong project management skills, knowledge of clinical research, and at least 3 years of experience. Join a dynamic team committed to innovation and growth opportunities.

Qualifikationen

  • At least 3 years in clinical research management within the pharmaceutical, biotech, or CRO industry.
  • Knowledge of GCP, ICH, FDA, and Canadian regulations.
  • Proficiency in Microsoft Office; strong organizational and problem-solving abilities.

Aufgaben

  • Communicate project information to stakeholders including the Sponsor, vendors, and internal team members.
  • Track and manage plans to ensure all deliverables and milestones are met.
  • Manage the quality of work and provide project status updates.

Kenntnisse

Communication
Organization
Problem-Solving

Ausbildung

B.Sc. in a related field

Tools

Microsoft Office

Jobbeschreibung

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Job Title: Associate Project Manager

The Associate Project Manager is involved in all phases of clinical trial project management. This person works closely with the Project Manager and functional team members. The Associate Project Manager is responsible for tracking the study budget, project scope, and timelines in accordance with applicable SOPs, good clinical practices, regulatory, and study-specific requirements. The Associate Project Manager will communicate project information to stakeholders, design templates, create presentations, review and edit project deliverables, and maintain the project information repository. They will also help resolve project conflicts, identify resource requirements, and align the project team on project scope.

This role will be perfect for you if:

  • You can deliver results while using a disciplined approach to project management.
  • You are seeking the next career step to become a project manager.
  • You have knowledge of clinical research projects and want to continue learning.
  • Working in a science-driven and innovative organization with meaningful work is important to you.

Responsibilities

  • Communicate project information to stakeholders including the Sponsor, vendors, and internal team members.
  • Track and manage plans to ensure all deliverables and milestones are met.
  • Coordinate tasks and deadlines across departments.
  • Manage the needs and expectations of the Sponsor and other stakeholders.
  • Train team members on the project.
  • Plan activities and resources required for the project.
  • Manage the quality of work.
  • Provide project status updates.
  • Analyze discrepancies and participate in corrective actions.
  • Enforce change control and risk management.
  • Develop and review operational plans and manuals.
  • Ensure study documents and deliverables meet requirements.
  • Participate in Investigator’s Meetings.
  • Support sites with necessary materials.
  • Oversee activities such as site selection, patient recruitment, regulatory submissions, clinical monitoring, and data management until database lock.

The company: Indero

Work environment

At Indero, collaborate with driven colleagues in a culture valuing innovation, reliability, and responsiveness. We offer a stimulating environment and growth opportunities.

Work location

This is a home-based position in Germany with regular travel required.

About Indero

Indero is a CRO specializing in dermatology, established in 2000, with a strong reputation for quality. Based in Montreal, we are expanding in North America and Europe.

We are committed to equitable treatment and will accommodate applicants with disabilities. Only applicants legally able to work in Germany will be considered.

Ideal Profile

Education: B.Sc. in a related field.

Experience: At least 3 years in clinical research management within the pharmaceutical, biotech, or CRO industry.

Knowledge & Skills: Knowledge of GCP, ICH, FDA, Canadian regulations; proficiency in Microsoft Office; excellent communication in English; French is a plus; strong organizational and problem-solving abilities; experience managing small to medium projects; team management skills.

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