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Associate Project Director, Warsaw

4 tygodni temu


Warszawa, Mazovia, Polska TN Poland Pełny etat

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials.

We seek an Associate Project Director (APD) to oversee and manage all aspects of clinical trials from start-up through final delivery for a range of therapeutic areas.

Main Responsibilities:
  • Strategic Planning: Develop and implement strategic plans for General Medicine trials, including defining project objectives, timelines, and resource allocation.
  • Trial Management: Oversee the planning, execution, and monitoring of clinical trials, ensuring adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Budget and Resource Management: Manage project budgets and allocate resources effectively, monitoring expenses, identifying cost-saving opportunities, and reporting financial progress to stakeholders.
  • Team Leadership: Lead and supervise a cross-functional team, fostering a collaborative and motivated work environment.
  • Regulatory Compliance: Stay up-to-date with evolving regulatory guidelines and ensure trials are conducted in compliance with relevant regulations.
  • Risk Management: Identify potential risks and develop risk mitigation plans to ensure trial success and patient safety.
  • Vendor Management: Select, contract, and manage external vendors and partners to support trial activities.
  • Data Management: Oversee data collection, analysis, and reporting activities, collaborating with data managers and biostatisticians to ensure data quality and integrity.
  • Safety Monitoring: Implement safety monitoring protocols and procedures, ensuring timely reporting of adverse events and appropriate interventions.
  • Communication: Maintain effective communication with internal teams, external stakeholders, investigators, and regulatory agencies, providing regular updates on trial progress.
  • Quality Assurance: Implement quality control processes and continuous improvement initiatives to enhance trial quality and efficiency.
Requirements:
  • Bachelor's degree in life sciences or a related field (advanced degree preferred).
  • Minimum 6 years of relevant work experience.
  • Strong knowledge of regulatory requirements and GCP.
  • Excellent project management, leadership, and communication skills.
  • Ability to analyze complex data and make informed decisions.
  • Excellent written and verbal communication, planning, critical thinking and organizational skills, including command of English language.
Benefits:
  • Comprehensive benefits package per location
  • Flexible Working hours (within reason)
  • Opportunity for remote working depending on location
  • Leadership and mentoring opportunities
  • Access to online soft-skills and technical training