Project Manager
Workplace: Beijing, Shanghai, Chengdu
Job Responsibilities:
1. Responsible for the comprehensive management, quality control, and supervision of the projects under your charge, ensuring timely and high-quality project delivery.
2. Responsible for providing business guidance and overseeing the execution of CRA activities within this project team, including: reviewing work plans and summary reports, assigning tasks to CRAs, promptly addressing issues arising from various centers and researchers, monitoring inspection quality, reviewing inspection reports, conducting real-time monitoring of key and challenging issues in the project, proactively identifying project risks and developing corresponding mitigation measures, supervising and ensuring adherence to project schedules, and managing materials and documentation.
3. Responsible for team-building efforts within this project team.
4. Assist the department manager in refining departmental policies and upgrading Standard Operating Procedures (SOPs), support the smooth implementation of new policies, and take the lead in effectively complying with the company’s relevant management regulations.
5. Responsible for training CRAs on project-related topics, encouraging CRAs to actively acquire professional knowledge and project management skills, and continuously enhancing their inspection capabilities.
6. Responsible for cost control of the project, strictly controlling unnecessary expenditures, and ensuring the efficiency and quality of CRA inspections.
7. Coordinate externally with various research centers, sponsors, data management personnel, and statisticians, maintaining good communication and fostering strong relationships with all parties.
8. Maintain effective communication and coordination with supervisors, other project teams, and departments; keep in touch with CRAs stationed overseas within the team, ensuring the smooth progress of the project.
Job requirements:
Educational Background: Bachelor’s degree or above in a medical or pharmaceutical-related field.
Work Experience: More than 3 years of experience in the management of clinical trials for multiple projects; prior experience in innovative drug project management is preferred.
Skills and Competencies: Familiar with the Regulations on Drug Registration, GCP guidelines, and other relevant regulations pertaining to clinical research.
- Proficient in the entire process of clinical research, with a deep understanding of all stages of clinical studies and the ability to work independently.
- Strong written and verbal communication skills, adept at interacting with researchers of various types.
- Possesses strong organizational, coordination, communication, and problem-solving abilities.
Benefits: Five social insurances and one housing fund, equity incentives, project awards, paid annual leave, weekends off on Saturdays and Sundays, regular medical checkups, and holiday benefits.
Submission email: ouyahuizhi-hr@healtech.com.cn