- Leadership of group work and building the team spirit, including developing team style and behaviour
- Ensuring adequate resources for the studies assigned
- Ensure that the workload of the team(s) or direct reports is adequate
- Ensure all direct reports complying with company policy and code of conduct
- Development and performance management of the team(s) or direct reports
- Ensure that the everyone in the team or direct reports have development and training plans, according to IDP process
- Contribute to high quality feasibility work
- Contribute to efficient SMOT organisation and its functioning at country level by working closely with responsible SMOT Director.
- Contribute to the quality improvement of the study processes and other procedures.
- Plan and organise coaching of the team members and all direct reports
- Ensure that the individual performance planning and review process is completed for all direct reports
- Prepare salary and bonus proposals of all team members or direct reports based on their performance in close collaboration with responsible SMOT Director and HR partner
- Ensure all systems are continuously updated.
- Support direction to LSM/teams on major study commitments including resolving any key issues identified.
- Review of monitoring reports/follow up letters to evaluate all direct reports capability as needed
- Perform necessary accompanied site visits for direct reports, supporting ongoing coaching and development.
- Support SMOT region in initiatives/activities as agreed with SMOT Director(s).
- Assist SMOT director to drive cross team projects, contribute more to team/org. learning, etc.
- University degree in biological science or healthcare-related field, or equivalent.
- Minimum 6 years experience in Clinical Operations (CRA / Sr. CRA / LSM) or other related fields.
- Proven team building and people/organizational development skills.
- Excellent knowledge of spoken and written English.
- Good ability to learn and to adapt to work with IT systems.
-
AstraZeneca Daxing District, 中国 全职Responsible for products' clinical development strategy and plan in multiple disease areas in R&D China. Responsible for managing reginal or China therapeutic or research projects or acting as an expert involved in the design, conduct, monitoring, data interpretation and reportin ...
-
AstraZeneca Daxing District, 中国 全职As a Regulatory CMC Expert, this role is responsible for assisting RA CMC Director to develop and communicate CMC regulatory strategy based on understanding of local CMC regulations, involved in CMC regulatory project, providing the support and coordination on CMC dossiers prepar ...
Clinical Research Manager - Daxing District, 中国 - AstraZeneca
描述
Requires in depth knowledge and experience of a specialist field and will be recognised expert. Works independently requiring only minimal guidance. Solves complex problems and takes a new perspective using existing solution. May act as a coach or team leader for technicians or lower level scientists.Major Responsibilities
Education, Qualifications, Skills and Experience
Date Posted
11-3月-2024Closing Date
29-6月-2024