Sr. Manager, Systems and Process Lead

Not Interested
Bookmark
Report This Job

profile Job Location:

Warsaw - Poland

profile Monthly Salary: Not Disclosed
Posted on: Yesterday
Vacancies: 1 Vacancy

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: Summary

We are seeking a highly skilled and experienced individual contributor to join our team as a Business Operations Lead. The successful candidate will be responsible for providing in conjunction with functional subject matter experts expertise in clinical development operations requirements understanding of assigned clinical business systems aligning with process owners and embedded within the respective GDO/GDM functions. This Business Operations Lead will be representing the end-user needs of the global data management organization to the Drug Development BI&T organization.

Key Responsibilities

  • Provide subject matter expertise in utilization of clinical business systems that support clinical development operations focused on Global Data Operation (GDO) Global Data Management (GDM) and regulatory compliance.
  • Understand clinical business systems and capabilities for Global Data Management with a focus on electronic data capture (EDC) external data acquisition clinical data review medical coding and electronic clinical health outcome (eCOA).
  • Drive the operation and continuous enhancement of EDC URLs serving as the accountable business owner and technical expert with evolving business needs.
  • Support the development and execution of automation innovation and digital data capture strategies which may include eSource technologies decentralized clinical trials (DCT) and mHealth.
  • Align with process owners to ensure that utilization of our clinical business systems is conducted in accordance with established processes and procedures.
  • Align within respective GDO and GDM functions to represent the end-user needs of Global Data Management (GDM) to the Drug Development BI&T organization including business strategy business requirements user testing and implementation of new systems and enhancements.
  • Collaborate with cross-functional teams and vendors to ensure that clinical development operations are conducted efficiently and effectively.
  • Stay up to date with industry trends and best practices in the utilization of business systems.
  • Provide input on training content and learning management systems curriculum
  • Provide final business regulatory and administrative approvals per applicable SOPs
  • Actively participate in multiple aspects of User Acceptance Testing including scenario planning scripting and coordination with business users
  • In collaboration with process owners and process leads create and maintain any applicable process and workflow documentation
  • Serve as a point of contact for compliance related activities including inspection support corrective and preventive actions data integrity and audit trails reviews
  • Where a capability spans multiple user groups or functions facilitate the collection of business and user requirements
  • Proactively resolve technical and process issues with cross functional teams to drive process optimization and operational efficiency.


Qualifications:

  • Bachelors degree in related fields such as life sciences computer science or business administration.
  • Minimum of 5 years of experience in clinical development operations with a focus on clinical data management and regulatory compliance.
  • Must have a strong understanding of the process and primary clinical business systems utilized by their functions (EDC data acquisition data review and eCOA platforms).
  • Excellent communication and interpersonal skills with the ability to collaborate effectively with cross-functional teams.
  • Strong analytical and problem-solving skills with the ability to identify and resolve complex issues.
  • Ability to work independently and manage multiple priorities in a fast-paced environment.
  • Experience with project management methodologies and tools is a plus.

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.

Compensation Overview:

Warsaw - PL: zł283330 - zł343330

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay takes into account characteristics of the job such as required skills where the job is performed the employees work schedule job-related knowledge and experience. The final compensation will be determined based on demonstrated experience and in accordance with pay equity principles and applicable employment laws.

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

We will never request payments financial information or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R: Sr. Manager Systems and Process Lead

Required Experience:

Manager

Working with UsChallenging. 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 breakthrou...
View more view more

About Company

Company Logo

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

View Profile View Profile