Bristol Myers Squibb Sr. Disease area specialist (oncology, phase 1) in Shanghai, China

Major Responsibilities:

  • Engage cross-functional and global colleagues in setting up phase 1 clinical development strategy in IO/oncology

  • Clinical expert in design, conduct and data interpretation of clinical trials, especially phase 1trials

  • External focus by engaging HA, KOL networking and innovative partnering with academia and other pharma companies

Qualification Requirement:

  • MD AND clinical or preclinical experience in oncology AND pharma clinical development experience in oncology.

  • Hand-on experience as study physician in managing trial design, EC, study setup, medical monitoring, reporting, data interpretation and publication

  • Experience of leading in clinical development strategy for China is preferred

  • Experience of designing and handling phase 1 clinical trial in IO/oncology is preferred

  • Proven ability of cross-functional collaboration, KOL networking and global colleague engagement

  • Good interpersonal skill, can-do attitude

  • Good language skill in English and Mandarin (verbal and written), good computer skill

Leading Compliance & Integrity Culture

  • Embrace BMS culture of integrity and strictly adhere to BMS policy, BMS White Book and Standards of Business Conduct &Ethics.

  • On a consistent (i.e., weekly or bi-weekly) basis, speaks with the team about the importance of compliance and integrity, and creates pride in BMS’s commitment to compliance;

  • On a quarterly basis, provides compliance training to the team; answer the team’s compliance questions, or refers them to an appropriate resource if s/he doesn’t know the answer;

  • Actively monitors the team members to prevent non-compliant behavior and looks into details before approving any expenses

  • Provides constructive suggestions to improve the BMS China compliance program

  • Is a compliance role model and leads by example.

  • Takes accountability to own organized events and provides adequate documentations. If organizes any event, must comply with all company policy and makes sure all activities are closed within 90 days after the event date. If subordinates are responsible for organizing events, must monitor the responsible person close PO’s within 90 days after the event date.

  • Is Compliant with the norms of the business communication, ethics, subordination, regulations of the confidentiality.

Leading Self:

  • Proactively obtains and innovatively refines the information including external market trends and the internal rules and regulations, internal procedures, messages, goals and vision of the management of the organization and shares relevant information with the team and colleagues timely to achieve company goal.

  • Timely performs tasks, orders and instructions of the manager.

  • Escalates / Reports to the manager of the department or function about all the challenges and shortcomings within Employee’s power and competency.

  • Proposes motions for the work development related to the Role.

  • in English and Mandarin (verbal and written), good computer skill

We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.

Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled