上海招聘

Interested candidte please visit the following URL to apply for the job online (候选人请务必点击以下链接进行在线申请):

https://sjobs.brassring.com/2052/ASP/TG/cim_jobdetail.asp?partnerid=13617&siteid=5271&jobid=1526998&codes=CN14

Job Description:

Provides operational leadership to the EPT, beginning at preclinical development stage (sPoC) and continuing through clinical proof-of-concept (PoC) and transition to Full Development. Drives the process for the development and maintenance of the integrated strategic and operational plan, under the guidance of the CPL and in collaboration with the EPT. Ensures organizational alignment and seamless execution of the development plan by the EPT. Facilitates team building and enhances team interactions and collaboration, striving for high performing EPTs.

1. Drives the process for the elaboration, maintenance and execution of the integrated development strategy for one or more biopharmaceutical programs beginning at preclinical development stage and continuing through clinical proof-of-concept (PoC) and transition to Full Development.

2. Develops the operational plan together with the Program Team, incl. realistic timelines, budget and resources planning, risk assessment and contingency planning

3. Ensures cross-functional alignment at Program Team level and organizational support for the execution of the operational plan by facilitating OTM internal and external stakeholder management

3. Is responsible for monitoring and tracking the Program Team performance, and ensures adherence to agreed upon team objectives and deliverables

4. Is responsible for comprehensiveness and quality of program information in the internal systems, databases, and communication to Senior Management (e.g.dEIS, IMB Updates, Research Monthly Updates)

5. Expected to identify bottlenecks, surface issues, and proactively drive for their resolution. Leads contingency planning efforts on behalf of the Program Team.

6. Leads ad-hoc cross-functional task forces as needed aiming at issue resolution

7. Is accountable for accurate forecasting, tracking and adherence to program budget (headcount and external costs) by liaising with EPT members. Challenges assumptions, timelines and expenses on program level across all LFs in Program Team.

8. Manages project variance and root cause analysis, develops risk mitigation / issue management plans with the objective to meet the financial targets

9. Ensures quality, up-to-dateness and accuracy of all program specific planning data (headcount, external costs, timelines) in Succeed and other data sources, incl. ClinAdmin

10. Manages and tracks implementation of publication plan

11. Ensures effective, proactive and open communications, horizontally and vertically, in order to achieve transparency and clarity of program goals, progress and issues.

12. Attends the Clinical Trial Team ensuring alignment with Program Team and overall program strategy

13. Provides operational excellence and support to the Program Team

14. Responsible for effective and efficient Program Team meetings, by i) providing meeting agenda and prereading material in timely fashion, ii) facilitating the decision making process at Program Team level, iii) capturing decisions, issues and action items in the minutes and iv) diligently following open on open action items

15. Identifies and resolves conflicts at Program Team and functional team level. Moderates the Team Launch Event and is responsible for the regular Team Survey execution and analysis at Program Team

16. Consolidates and tracks project termination plans

17. Ensures smooth transition of program to Full Development

Keywords: CNIBR, NIBR Shanghai

Minimum requirements:

1. 5+ years in the pharmaceutical industry

2. At least 3 yrs equivalent multi- / cross-functional leadership experience

3. Advanced Project Management skills

4. Clinical operations experience of advantage

5. Previous work and leadership experience in international and multidisciplinary biopharmaceutical drug development teams and broad operational experience with an understanding of drug development process, preferably for biopharmaceutical products

6. Advanced level of basic science. Detailed knowledge of special requirements in a given TA/BU

7. Advanced knowledge of drug development process

8. Advanced knowledge of regulatory and business requirements.

9. Detailed knowledge of international customs and business practice

10. Understands basic financial aspects, including knowledge of resource planning (headcount and budget) and management

9. Ability to critically and objective interpret and evaluate scientific and competitive, business related information.

10. Expert planning and tracking skills, able to see big picture, well-organized, focused on results, capable of managing multiple projects, excellent time management with respect to priorities and self-management

10. Advanced leadership skills

11. Strong interpersonal and communication skills for bridging between scientific and business participants, for negotiating timelines and for effective international collaboration. Strong verbal communication. Expert in written communications..

12. Expert team player

诺华（Novartis AG）是全球医药保健行业的领导者。其核心业务涉及专利药，非专利药，眼睛护理，消费者保健和动物保健等领域。诺华公司总部设在瑞士巴塞尔，业务遍及全球140多个国家和地区。

诺华（中国）生物医学研究有限公司是诺华全球研发组织――诺华生物医学研究所（NIBR）的第八个研究基地。我们位于中国上海市张江高科技园区，将成为诺华在亚洲的主要研究中心，以及除在欧美的研究中心外的最主要的研究中心。我们的研究和探索开发活动的重点是发现并开发创新疗法，用于治疗在亚洲远未达到医药需求的疾病。我们与从不同之处在于将专注现代药物的发现和开发方法的研究。最初阶段，研发工作将专注在引起中国地方性癌症的感染原因。我们还将开展临床试验，进行安全性研究，生物标志物和检测分析，表达谱、生物分析以及转化医学的研究。

随着公司业务的迅速扩展，我们热忱欢迎您的加入。同时我们将提供具有竞争力的薪酬福利待遇以及良好的培训发展机会。