Senior Project Manager (MJ000033)
Key Responsibilities:
- Clinical Operations Execution and Management
- Support the delivery of quality studies within assigned timelines by assisting in end-to-end study clinical operations activities, including but not limited to start-up, protocol design, feasibility, site management, recruitment strategy, monitoring, and regulatory and ethics review, in collaboration with internal and external stakeholders.
- Contribute to operational excellence and efficiency through effective resource support and application of local best practices.
- Assist in coordinating resources within the country to improve operational efficiency.
- Operational System Support
- Help optimize the operational system by leveraging HQ systems and supporting regional teams through training, role clarification, and routine monitoring.
- Support the development and maintenance of SOPs and Working Instructions for clinical monitoring at the country level.
- Participate in quality checks and follow-up on open issues to ensure compliance with required systems and documentation.
- Compliance and Training
- Support full compliance within the team through training and regular qualification monitoring.
- People and Team Support
- Support the operational team by assisting in motivation and development efforts. Provide guidance and support to team members, demonstrating Tigermed’s values through action.
- Participate in interviews and contribute to hiring decisions for key roles.
- Help improve overall employee engagement within the team.
- Bidding and Strategy Support
- Assist in bidding activities, organize and participate in local stakeholder meetings, and collaborate with expert panels to help develop optimal strategies/solutions.
Minimum Qualifications:
- Education
- Bachelor’s degree or above in Medical, Pharmacology, or Biology-related fields.
- Professional Skills
- Solid understanding of clinical trial regulations, GCP, and clinical trial operations. GCP certification required.
- Knowledge of new technologies and industry trends is preferred.
- Work Experience
- At least 5 years of clinical trial experience, with CRO management experience preferred.
- Language Skills
- Fluent in both oral and written English.
- Computer Skills
- Proficient in Microsoft Office applications (Word, Excel, PowerPoint).
- Other Competencies
- At least 3 years of people management or team coordination experience.
- Strong communication, writing, and presentation skills.
- Commercial awareness with the ability to provide strategic recommendations and solve problems from a company-wide perspective.
- Cultural Requirements
- Integrity & Honesty; Open and Inclusive; Cooperation & Accountability; Professional Innovation.