Site Contract Specialist
Buenos Aires - Argentina
Job Summary
Working with Us
Challenging. Meaningful. Life-changing. Those arent 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. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope alongside high-achieving teams. 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: Myers Squibb es un empleador que brinda igualdad de oportunidades. Las personas que apliquen para cualquier vacante y que estén calificadas para la misma recibirán consideración para el empleo sin distinción de raza color religión sexo orientación sexual identidad de género nacionalidad edad discapacidad condición de veterano protegido embarazo ciudadanía estado civil expresión de género información genética afiliación política o cualquier otra característica protegida por la ley.
Position Summary
Executes the end to end preparation negotiation and finalization of site contracts and investigator budgets within established SOPs multilingual templates fallback language and approval matrices. Maintains complete and timely documentation in approved systems and collaborates with cross functional partners to support on time contract execution. Exercises decision authority on budget items up to the defined threshold per SOP; non standard terms out of threshold items and complex/legal risks are escalated to negotiation governance lead or management as applicable.
Duties/Responsibilities
Prepare review negotiate and finalize site contracts and budgets using approved templates fallback language and country playbooks; ensure alignment with protocol requirements and study timelines.
Apply SOP defined budget parameters and exercise decision making up to the authorized threshold; route exceptions and out of threshold items for approval per governance.
Ensure strict adherence to SOPs WI/playbooks approval matrices and confidentiality standards; escalate non standard clauses and risks to the appropriate stakeholder.
Collaborate with study teams Legal Finance CRO partners and other stakeholders to resolve routine contracting questions and progress negotiations within established guardrails.
Maintain accurate timely and complete records of negotiation status decisions and versions in required contracting systems (e.g. CLM/trackers e signature) enabling reliable dashboards and study reporting.
Meet established KPIs for cycle time quality and data accuracy; proactively flag risks to timelines and compliance.
Supports process improvement by identifying recurring issues and proposing practical enhancements; adopts new templates standards and tooling as rolled out by governance.
Conducts targeted reviews of prior negotiated agreements to identify new ways to improve efficiency within approved boundaries.
Reporting Relationship
Reports to Associate Director/Director Site Contracting Operations
Qualifications Specific Knowledge Skills Abilities
Working knowledge of clinical study protocols contract templates investigator grants and site budget negotiation processes; ability to negotiate within SOP defined guardrails and thresholds.
High attention to detail with strong organization and time management; able to manage multiple negotiations against agreed timelines.
Effective negotiation and communication skills in multinational multilingual settings; comfortable using approved translation resources/tools where applicable.
Proficiency with contract management systems and e signature platforms; strong MS Office skills.
Requirements
Bachelors degree in Life Sciences Business Administration or related field.
Minimum 2 years in site contract negotiation or clinical operations (or equivalent combination of education/experience).
Travel
Up to 10% travel for regional strategy meetings and cross-functional collaboration.
#LI-Hybrid
If you come across a role that intrigues you but doesnt 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 a supportive culture promoting global participation 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
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential site-by-design field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles onsite presence is considered an essential job function and is critical to collaboration innovation productivity and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
Supporting People with Disabilities
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 . Visit to access our complete Equal Employment Opportunity statement.
Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position please visit this page for important additional information: Protection
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R: Site Contract SpecialistRequired Experience:
IC
About Company
Bristol-Myers Squibb is a global biopharmaceutical company focused on discovering, developing and delivering innovative medicines for patients with serious diseases. Our medicines are helping millions of patients around the world in disease areas such as oncology, cardiovascular, immu ... View more