Sr. Outsourcing Manager
vor 2 Monaten
**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.
**Job Summary**:
This individual contributor role is responsible for managing task-level activities for both in-house and outsourced clinical studies, ensuring alignment with Bristol-Myers Squibb's (BMS) outsourcing strategies. The role supports vendor partnerships across various clinical trial service categories and ensures compliance with regulatory standards.
**Key Responsibilities**:
- Lead outsourcing activities, collaborating with operational teams, support groups, and service providers to select, contract, and execute outsourced studies while ensuring adherence to regulatory and ethical standards.
- Drive project success by meeting short-term objectives and maintaining adherence to project schedules.
- Support the Outsourcing team in areas such as alliance management, Financial/Resource accountability, and FSP operations.
- Address contractual issues in communication with business partners and internal stakeholders.
- Provide operational expertise, training, and support to teams on all aspects of outsourced work, ensuring alignment with BMS outsourcing strategies.
- Ensure team alignment with BMS outsourcing strategies to optimize project execution.
**Qualifications & Experience**:
- Bachelor's degree in Legal, Life Sciences, Business Administration, or a related field (advanced degree is a plus).
- 3 to 5 years of clinical development experience in the pharmaceutical, biotech, or CRO industry.
- Experience managing a variety of suppliers, including Contract Research Organizations, clinical laboratories, and service providers, with the ability to negotiate and execute legal and financial agreements.
- Proven experience managing internal and external stakeholders, gathering and incorporating feedback as needed.
- Ability to manage cross-functional and multi-cultural teams and work effectively within a matrix structure.
- Strong time management skills with the flexibility to handle multiple priorities and drive new initiatives.
- Adaptability to work in a dynamic and complex environment, maintaining high performance under changing conditions.
**Uniquely Interesting Work, Life-changing Careers**
**On-site Protocol**
BMS has a diverse 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.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
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