Site Contract Lead (1 Year Fixed term) [South Korea]


 

Bristol Myers Squibb에서 우리는 과학을 통해 환자의 삶을 변화시키는 단일 비전에서 영감을 받았습니다. 종양학, 혈액학, 면역학 및 심혈관 질환과 업계에서 가장 다양하고 유망한 파이프 라인 중 하나 인 우리의 열정적 인 동료들은 의미있는 변화를 주도하는 혁신에 기여합니다. 우리는 우리가 개척하는 모든 치료에 인간의 손길을 가져옵니다. 우리와 함께하고 변화를 만드십시오.

The Site contract lead is responsible for the end-to-end management of budgeting and contracting for Study Teams with a focus on contracting a variety of contracts & study types including Confidential Disclosure Agreements (CDAs), Investigator contracts for BMS sponsored studies, non-registrational / Investigator Sponsored Research (ISR) studies.


Responsibilities:

  • Provide knowledgeable single-point of service to study teams related to study budgets and contracts.

  • Prepare study /site level grant budgets.

  • Manage the end-to-end process for executing Clinical Trial Agreements (CTAgs) with investigator sites.

  • Prepare contract documents from templates and modify to reflect unique aspects of the particular study, including (the CTAg financial appendix).

  • Negotiate financial and legal aspects of CTAg and Master Service Agreements with sites, Institutions or vendor personnel.

  • Work with Legal as needed having been provided with training in legal fall-back language.

  • Clearly and efficient communication with BMS Clinical and Legal Teams regarding amendments and other issues

  • Enter CTAg, documents and data into Clinical Trial Management System and contract management software and ensure correct filing.

  • Preparation, negotiation and execution of Master Agreements with Institution.

  • Develop and maintain template language in collaboration with legal for all contract types. Would include maintenance of associated back-up language.

  • Escalate to appropriate BMS colleague when a significant risk to the business is identified.

  • Independently make appropriate business decisions within their scope or authority, and educate internal project leaders on the issues and risks associated with contracting decisions.

  • Ensure contracts are executed in alignment with trial deliverables and priorities.

  • Execute local purchase contracts if applicable (e.g. of drug, equipment).

  • Ensure all CTAgs and payments are accurately posted and ensure correct filing.

  • May support preparing invoices/payments due reports and managing, tracking and executing payments to investigator sites.


At the senior level of experience:

  • Serve as key resource for colleagues, by providing guidance, leading training and mentoring to other team members through a mentoring process using informal and formal presentations.

  • Proactively work with stakeholders assist in the resolution of complex issues both locally and/or globally.

  • Constantly analyses the budget negotiation/contract process, escalate issues and looking for innovative ways to introduce efficiencies in order to speed-up contract process.

Qualifications, experience & competencies

  • Bachelor's or Master's degree required within life sciences or related field.

  • Minimum 2 years’ experience negotiating legal and/or financial agreements, preferably in pharmaceutical industry clinical trials or 2 years of industry related experience in clinical operations/trials

  • Demonstrable capability to manage multiple activities at the same time and still can be in aligned with each study specific timeline

  • Working knowledge of clinical trial start-ups and finance cycles including knowledge of site needs and perspective.

  • Strong organization and time management skills and ability to effectively manage multiple competing priorities.

  • Strong communication skills with a strong customer focus, able to manage both internal and external clients at all organizational levels.

  • Strong negotiation and interpersonal skills including strong conflict resolution skills.

  • Good verbal and written communication skills (both in English and Korean).

  • Independent use without assistance (Microsoft Suite, Clinical Trial Management Systems (CTMS), SAP, Contract management software).

#LI-Hybrid

전 세계적으로 우리는 심각한 질병을 앓고있는 환자의 삶에 영향을 미치기 위해 열정적입니다. 포용적인 문화에서 우리의 개인 재능과 다양한 관점을 적용 할 수있는 권한을 부여받은 우리의 열정, 혁신, 긴급 성, 책임, 포용성 및 성실성의 공유 가치는 각 동료의 최고의 잠재력을 이끌어냅니다.

Bristol Myers Squibb은 업무 환경에서 균형과 유연성의 중요성을 인식하고 있습니다. 우리는 직원들에게 직장과 개인 생활에서 목표를 추구 할 수있는 자원을 제공하는 다양한 경쟁 혜택, 서비스 및 프로그램을 제공합니다


 

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