Assistant Project Manager
Health Data Specialists (HeaDS)
πριν από 3 μέρες
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Περιγραφή Θέσης

Health Data Specialists (HeaDS), an Athens, Greece based CRO with a global reach, is seeking an Assistant Project Manager for its international Clinical Trial operations.

The Assistant Project Manager role will be involved in multi-center global interventional Clinical Trials across multiple Therapeutic Areas, with key focus on Oncology / Hematology.

Job Description :

The Assistant Project Manager will :

  • Assisting in the planning and implementation of projects.
  • Provide support to the Clinical Project Manager on the technical, protocol-specific and operational aspects of assigned studies to ensure that project deliverables meet the agreed expectations.
  • Organize & oversee a cross-functional team in accordance with applicable project plans, SOPs, ICH / GCP and regulatory requirements.
  • Oversee performance of third party vendors.
  • Confirm and apply quality control activities.
  • Participate in the training and development of the clinical study team.
  • Evaluate and report the progress of the project to ensure that the timeline is followed steadily and consistently.
  • Review and approve site visit reports; ensure tracking, follow up and resolution of site issues has been completed in a timely manner.
  • Job Requirements :

  • Bachelor’s and / or master’s degree (in Health Sciences preferred)
  • Previous work experience :
  • o Minimum 3 years’ experience with clinical trial conduct as a CRA or other operational role

    o Experience in managing or coordinating international multi-center trials is highly desired.

  • Advanced user of Microsoft Office Suite; experience with project management software is desired.
  • Ability to handle complex projects; flexibility in managing changing priorities; strategic problem solving and judgement skills.
  • Capable of managing multiple projects, timelines and responsibilities.
  • Excellent written and verbal communication skills in English.
  • Ability to work with little direction.
  • Initiative taking and team working attitude.
  • Knowledge of ICH / GCP guidelines and regulatory requirements.
  • A genuine interest in the field of clinical development.
  • Willingness to travel approx. 20% of the time, including domestic and international travel.
  • Join us to be part of a multidisciplinary team of highly skilled professionals in the forefront of Clinical Research within a friendly work environment.

    Competitive remuneration package comes on top.

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