• The GSL is responsible for leading a cross-functional study team (core and extended) and for providing the team withdirection, guidance and study management plans to enable successful study delivery.

• The GSL is the main liaison between the study team and the Clinical Program Team (CPT),typically from Clinical Study Protocol (CSP) development/study handover through to close-out and archiving.

• The GSL is accountable to the CPT for the delivery of a study according to agreed timelines, budget and quality standards by ensuring an effective partnership and teamwork within study team and/or external partners.

• The GSL leads the study team and/or study oversight team in accordance with AZ’s Study Team Operating Model (STOM), Project Management Framework and/or clinical outsourcing models (e.g. SCOUT), current clinical trial regulations (e.g. ICH GCP), AstraZeneca Standard Operating Procedures (AZ SOPs), AZ policies and best practices (e.g. AZ guidelines) and in line with AZ values and behaviors

Essential:

• University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research

• 7 years of relevant clinical experience in the pharmaceutical industry, including 2 years’ project management experience, or equivalent combination of education, training and experience

• Extensive knowledge of clinical research regulatory requirements and demonstrated abilities in clinical study management processes and clinical/drug development

• Demonstrated solid project management skills and knowledge of relevant tools

• Strong, demonstrated abilities/skills in team leadership

• Strong abilities in establishing and maintaining effective working relationships with internal and external co-workers and stakeholders, along with strong conflict management skills

• Excellent communication and interpersonal skills

• Strong strategic and critical thinking abilities

• Strong organizational and problem-solving skills

• Ability to manage competing priorities

Desirable:

• Advanced degree, Masters level education (or higher)

• Project management certification

• Proven project management experience on a global level

• Experience in all phases of a clinical study lifecycle

• Proficiency in Microsoft Project

【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。】