Associate Director, Clinical Integration & Enablement

Bristol-Myers Squibb India Pvt Ltd

Hyderabad

Not disclosed

Work from Office

Full Time

Min. 8 years

Job Details

Job Description

Associate Director, Clinical Integration & Enablement, Clinical Supply Chain Business Capabilities

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. 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.

Position Overview:

The Associate Director of CSC Business Capabilities plays a pivotal role in overseeing and optimizing the functions within the Clinical Supply Chain (CSC). The Associate Director leads a team that provides Clinical Supply Chain (CSC) representation for Interactive Response Technology (IRT), Clinical Supply Chain Logistics (CSCL) and Business Operational activities related to CSC budget (IRT, CSCL, and Comparator), contract administration and financial metrics. This position requires a strategic leader capable of managing a team, optimizing budgets, supporting logistical operations in the APAC region and providing IRT study support.

Key Responsibilities:

  • Lead, mentor, and oversee a team of Managers and Specialists who support IRT, CSCL, and other CSC business capabilities.
  • Foster a culture of collaboration, innovation, and excellence, encouraging team members to achieve their full potential.
  • Business support for CSC operational activities:
    • Assist the Director of Clinical Integration and Enablement (CI&E) with compiling, maintaining, and monitoring the CSC portion of the R&D portfolio budget (inclusive of IRT, Logistics, and Comparator support) to achieve established CSC R&D Savings Targets.
    • Provide input into monthly budget projections and contribute to the preparation of formal corporate projections.
    • Oversee contracts administration, financial metrics and ad-hoc reporting for the CSC organization by leading individuals responsible for executing and managing contract activities, ensuring compliance, efficiency, value creation, and adherence to financial targets.
  • Logistical support and Operations Management:
    • Within the APAC region, oversee operations across a network of distribution centers, ensuring compliance with all applicable regulations and supporting the distribution needs of BMS clinical trials for Investigational Medicinal Products (IMPs).
    • Support the collection of relevant metrics, conduct analysis to support budget and expense management, vendor performance management, and continuous improvement goals.
    • Oversee Returns and Destruction operations across a network of distribution centers, ensuring compliance with all applicable regulations and supporting the compliance needs of BMS clinical trials for Investigational Medicinal Products.
    • Work with 3rd party and internal partners to monitor and drive returns and destruction reporting, evaluation, trending, and operational activities to reflect the BMS portfolio, business model, and evolving regulations.
  • IRT Study Support and Vendor Management:
    • Ensure an excellent level of support and service is provided by on site IRT personnel to promote seamless execution and alignment with IRT study objectives.
    • Support time zone appropriate departmental audits. 
    • Manage vendor contractual obligations in conjunction with Global Procurement through documents such as Master Services Agreement, Quality Agreement, Service Level Agreement, rate cards, etc
  • Additional tasks within scope of expertise and experience as assigned by the supervisor in pursuit of BMS goals.
  • Evaluate and refine operational processes to yield strategic improvements, cost savings and operational efficiencies.
  • Provide regular feedback to division and departmental heads of personnel within IRT, CSCL, and other CSC business capabilities functions.

Qualifications:

  • Undergraduate/graduate degree in business, science, supply chain management or related field.
  • Certification in supply chain, clinical research, or logistics (e.g., PMP, Lean Six Sigma, APICS) is preferred.
  • Minimum of 8 years of relevant experience in supply chain operations, logistics, budget management, operational excellence, or related fields in the pharmaceutical or biopharmaceutical industry.
  • Demonstrated ability to lead, mentor, and develop a high-performing team while fostering collaboration and honing individual strengths.
  • Strong interpersonal skills to drive team engagement and lead organizational change initiatives.
  • Proficiency in managing financial operations, budgeting, and contract administration.
  • Expertise in facilitating and overseeing Interactive Response Technology (IRT) studies and systems is highly desirable.
  • Thorough understanding of supply chain logistical systems, including transportation, distribution, returns, and destruction across multiple regions is highly desirable
  • Strong knowledge of clinical trial processes and Investigational Medicinal Products (IMPs) handling.
  • Experience in driving regulatory compliance across functions.
  • Effective conflict resolution and relationship management skills across departments and external partners.
  • Ability to oversee multiple ongoing projects, prioritize timelines, manage resources, and align projects with organizational goals.
  • Advanced organizational skills, negotiation skills and attention to detail. 
  • Excellent communication skills, both verbal and written. 
  • Proficient with MS Office suite

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 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.

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 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.

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: https://careers.bms.com/california-residents/

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

Experience Level

Mid Level

Job role

Work location

Hyderabad, India

Department

Healthcare / Doctor / Hospital Staff

Role / Category

Hospital Admin

Employment type

Full Time

Shift

Day Shift

Job requirements

Experience

Min. 8 years

About company

Name

Bristol-Myers Squibb India Pvt Ltd

Job posted by Bristol-Myers Squibb India Pvt Ltd

Apply on company website