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


 

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

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

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.


 

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