Aktualne oferty pracy związane z Associate Project Director, Warsaw - Warszawa, Mazovia - TN Poland
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Associate Project Director
1 dzień temu
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Senior Sales Director in Warsaw
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Global Associate Director, Procurement FP&A
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Project Director
6 dni temu
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Project Director
6 dni temu
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Associate Director, Attack Surface Reduction
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Corporate Project Director
5 dni temu
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6 dni temu
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Senior Project Director
5 dni temu
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6 dni temu
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5 dni temu
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Technical Project Director
8 minut temu
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Art Director
1 dzień temu
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Equinix Operations Director
2 dni temu
Warszawa, Mazovia, Polska TN Poland Pełny etatAre you looking for a challenging role that allows you to make a real impact? Do you have experience leading cross-functional teams and driving business results? We are seeking an experienced Equinix Operations Director to join our team in Warsaw, Poland.About the RoleThe Equinix Operations Director will be responsible for overseeing the operations of our...
Associate Project Director, Warsaw
4 tygodni temu
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.
- 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.
- 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