Key Responsibilities:

1. Cross-Functional Team Membership

• Can lead and/or otherwise represents CD in sub-teams (e.g. Study Management Teams)

• relevant to assigned molecule(s)/indication(s) and helps ensure cross-functional

• integration, coordination and alignment to enable effective and efficient CD plan execution.

• Accountable for training new CST members.

• May also, as appropriate, support relevant sub-teams in assigning and training new team members.

• As appropriate, participates in ongoing enhancements/development of core and sub-team processes, structures, systems, tools and other resources.

• Where applicable, may manage one or more direct reports and is, in such instances, responsible for hiring, training, developing and retaining talent on his/her staff.

• Consistently complies with all governing employment laws, regulations and company HR policies & procedures.
  
  

2. Global Clinical Development Planning

• Maintains the highest standards and levels of scientific and clinical knowledge in clinical oncology.

• Develops and provides clinical science information for inclusion into the Integrated.

• Development Commercialization Plan (IDCP), and China assessments on the pre-LIP

• molecular as part of Development Acceleration deliverables.

• Represents CD for the assigned molecule(s)/indication(s) to other internal Roche groups.

• Participates in CD strategy development and may present to various internal committees.

• Responsible for creating and implementing the CD plan for assigned molecule(s)/indication(s) and/or other programs: 1)Seeks guidance from his/her manager, as and when needed, to ensure appropriate design and development of the CD plan; 2) Responsible to ensure strategic and operational alignment of the CD plan with the relevant CD strategy, strategic and annual LCPs; 3) Guides CST and relevant sub-teams in developing all CD plan components (e.g., analytics/data strategy, KOL development, publications strategy, etc.); 4) Works with CST and other relevant teams to develop and provide information and input for budget/resource requirements necessary to implement and execute the CD plan

• Collaborates with a variety of internal and external partners and stakeholders, such as clinical investigators, clinicians, scientists and key opinion leaders (KOLs), as well as multidisciplinary internal groups, including other groups in PD, research, business development, commercial operations, legal, etc.

• Communicates with HAs, as and when needed, or otherwise appropriate. Ethically, effectively and professionally represents the interests of Roche and patients. Escalates matters, as needed, in a timely manner to his/her manager or other internal partners/stakeholders.

• Stays abreast of internal and external developments, trends and other dynamics relevant to the work of CD to maintain, at all times, a fully current view and perspective of internal/external influences and/or implications for the assigned therapeutic and disease area(s).
  
  

3. Clinical Development Plan Implementation

• Provides clinical oversight across all relevant studies and programs

• Develops and delivers key presentations, both internally and externally, to convey the CD perspective and provide updates on strategies, plans and other activities. Includes presenting at advisory boards and other relevant external forums representing Roche.

• Drives ongoing data generation to address unmet medical needs and recommend new or extended CD studies or other programs to his/her manager and others in the relevant therapeutic area of assignment.

• Responsible to ensure that CD plans, objectives, and deliverables are consistently accomplished on-time and on-target.

• Completes and/or leads other special projects, as and when assigned, or otherwise requested.

• Consistently complies with, and ensures the same among relevant CST members, all governing laws, regulations, Roche Standard Operating Procedures (SOPs) and other guidelines.
  
  

Qualifications & Experience:

• M.D. with at least 3 years of clinical experience in oncology

• 3 or more years pharma-industry experience, with focusing on clinical trials.

• In-depth understanding of Phase II – III drug development, knowledge/understanding of

• Phase I & IV drug development is a plus

• Experience authoring a full clinical study protocol is preferred

• Comprehensive understanding of clinical oncology, understanding/experience on molecular biology is a plus

• Familiar with competitive activity in oncology

• Experience working with the principles and techniques of data analysis, interpretation and clinical relevance (e.g., ISS, ISE, competitor data, etc.)

• Versed in medical aspects of GCP (Good Clinical Practice), ICH (International

• Conference on Harmonisation of Technical Requirements for Registration of

• Pharmaceuticals for Human Use), FDA, EMEA, NICE and other relevant guidelines and regulations
  
  

Abilities:

• Has impeccable ethics. Demonstrates, or proven abilities to demonstrate, Roche Values

• Outstanding attention-to-detail

• Has sound knowledge of the pharma/biotech industry, the multiple functions and roles involved in the drug development process. Can effectively contribute to development of disease strategies and plans

• Excellent project management skills: can prioritize multiple tasks and goals and ensure the timely, on-target and within-budget accomplishment of such

• Strong interpersonal, verbal communication and influencing skills: can influence without authority and has proven experience building and cultivating relationships with key partners and stakeholders, both internally and externally

• Fluent in English communication

• Excellent written communication skills

• Strong business presentation skills: effective at summarizing and presenting the key considerations and decision-points

• Confident and competent when interacting with varying levels of internal/external management, KOLs, etc.: stays focused and on-point, is able to raise problems or challenges in a productive and mature manner

• Strong negotiation skills: can effectively drive discussions and decisions toward desired end-results

• Strong orientation to teamwork
  

 

企業介紹:

　　迪醫獵頭（www.021tcjzsj.com）于2003年成立，由幾個海外歸來的獵頭顧問創建，我們服務于藥品、醫療器械、醫院管理，保健品，還有生物工程，專業專注于醫藥衛生行業是我們的目標，我們的團隊成員由多位經驗豐富的具有醫藥醫療企業背景的獵頭顧問組建而成，主要為國際（內）醫藥企業提供中、高級人才尋訪，即獵頭服務。

　　我們的獵頭顧問均會依靠個人的“能力”、“經驗”、“努力”完成任務，我們關注職位成功率和職位完成時間，我們的目標是：“90%職位成功率”和“1-2周之內完成待聘職位初次推薦”。

　　迪醫獵頭總部位于北京，并通過設在各地的合作伙伴及網絡，提供完善的獵頭服務，因為專業和專注，有效提高了工作效率，降低了過程成本，從而間接降低客戶成本。因為事先關注成本，所以我們向客戶進行收費時，通常按行內最低標準進行收取，盡可能保證客戶的利益。

　　迪醫獵頭，專業醫藥人才資源服務機構。我們吸引了成功的醫藥獵頭顧問，我們擁有高端行業和高端職能崗位相關的專業技術，醫藥獵頭顧問的出眾才智改進您的招聘程序，并且使您的公司更好地了解市場和競爭狀況。

　　迪醫獵頭致力于招募全球最優秀的醫藥高級人才，為優秀的企業提供最合適的醫藥人才，品質成就品牌，迪醫獵頭專業醫藥獵頭全力打造醫藥界高端人才的供需平臺！