Job Description

1. Education: Master's degree in Life Sciences, Medicine, or a related field; advanced degree preferred.
2. Experience: Minimum of 10 years of experience in clinical project management within the pharmaceutical, biotechnology, or CRO industry.
3. Global Trial Experience: Proven track record of managing international clinical trials across multiple regions.
4. Regulatory Knowledge: Thorough understanding of global regulatory requirements and guidelines.
5. Strong Leadership: Demonstrated ability to lead and motivate cross-functional teams in a matrix environment.
6. Communication Skills: Excellent verbal and written communication skills, with the ability to effectively present complex information to diverse audiences.
7. Problem-Solving: Strong analytical and problem-solving skills, with a focus on innovative and pragmatic solutions.
8. Time Management: Exceptional organizational and time-management skills, capable of managing multiple priorities and deadlines effectively.
9. Adaptability: Ability to thrive in a fast-paced, dynamic environment with a proactive approach to change management.
10. Language Proficiency: Proficiency in English (written and spoken); additional languages are a plus. 1. Project Management: Lead and manage global clinical trials, collaborating with cross-functional teams to ensure projects are executed efficiently and effectively.

1. Planning: Develop comprehensive project plans, including timelines, resource allocation, and risk assessment, to achieve study objectives.
2. Budgeting: Oversee project budgeting, ensuring adherence to financial guidelines and cost-effective management of resources.
3. Site Selection: Work with teams to identify and evaluate potential clinical trial sites, ensuring compliance with regulations and ethical standards.
4. Vendor Management: Collaborate with external vendors and contractors to ensure seamless study operations and delivery of quality services.
5. Protocol Development: Provide input in the development of study protocols, ensuring alignment with regulatory requirements and study objectives.
6. Regulatory Compliance: Ensure adherence to all relevant regulatory guidelines and requirements across multiple regions.
7. Quality Control: Implement robust quality control measures to monitor data integrity and maintain high-quality standards throughout the study.
8. Risk Management: Identify potential risks and implement mitigation strategies to minimize any impact on study timelines and objectives.
9. Stakeholder Communication: Maintain effective communication with internal and external stakeholders, providing regular updates on project progress.
10. Reporting: Generate timely and accurate progress reports, presenting findings to senior management and clients as required.

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