(Associate) Clinical Research Manager - North region
Major Responsibilities
- 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/activitiesas agreed with SMOT Director(s).
- Assist SMOT director to drive cross team projects, contribute more to team/org. learning, etc.
Education, Qualifications, Skills and Experience
- 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/organizationaldevelopment skills.
- Excellent knowledge of spoken and written English.
- Good ability to learn and to adapt to work with IT systems.
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised. 阿斯利康是一家提供平等机会的企业，我们将考虑所有符合条件的求职者就业。不因残疾、性别或性取向、怀孕或产假状况、种族或民族或族裔出身、年龄、宗教或信仰、性别认同或变更、婚姻或伴侣关系、受保护的退伍军人身份（如果适用）及任何其他受法律保护的特征而产生歧视。
Date Posted
10-6月-2026Closing Date
29-9月-2026AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.