Manager, Veeva Clinical Engineering & Operations - Bristol Myers Squibb
Princeton, NJ
About the Job
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 .
Position Summary:
Accountable for implementing and supporting strategic information systems that enable Global Development Operations (GDO), specifically focusing on Veeva Clinical Vault (Veeva CTMS, Veeva eTMF). This role, under the supervision of the Veeva Engineering Lead, will be responsible for identifying, designing, and developing solutions to meet the continuous demand within GDO-IT, as well as managing the build and run of these technology assets, ensuring they are reliable, accessible, & secure.
Specific responsibilities:
+ Partner with GDO-IT Engineering Leads and IT Product Managers to plan, prioritize, deliver & support strategic digital capabilities and ensure maximum value is achieved.
+ Support Veeva Engineering lead in collaborating with the GDO-IT product teams and assist in identifying, designing, and developing technical solutions to meet business demand
+ Manage the build and run of technology assets.
+ Assist with technical work related to data quality issues, data correction, data load, etc.
+ Provide Audit/ Inspection support
+ Provide L2/L3 support for Veeva CTMS and eTMF application for time sensitive support tickets
+ Work with the vendor for any major issues/bugs in the applications
+ Understand the integrations thoroughly and work with the integrated teams (internal & external) for any issues.
+ Drive process optimization to bring efficiency
Requirements:
+ Must have a minimum of 6 years of related work experience in a Biopharmaceutical environment.
+ BS/BA in Engineering, Computer Science or Life Sciences (or other quantitative related discipline).
+ Must have Veeva Clinical Vault expertise, with specific knowledge of Veeva CTMS and eTMF.
+ Must have broad technology expertise, good working knowledge of Pharmaceutical R&D business processes, particularly in Clinical Trial Operations, with demonstrated command of key concepts, systems and processes.
+ Preferred - certified in Veeva Vault Administration
+ Preferred to have experience / understanding of GxP validation SDLC process.
+ Demonstrated competency in execution of multiple large projects simultaneously within a Product Model leveraging Agile methods.
+ Critical thinking to investigate issues with systems and data, and identify solutions for short-term remediation and long-term strategy.
+ Experience in evaluating new technologies, delivery methods (e.g., SaaS/PaaS/IaaS), and services, and contributing towards the design and implementation of those new solutions.
+ Ability to achieve successful consensus among differing priorities and stakeholders in both the IT and Business communities.
+ Must be a relationship builder and capable of working effectively in a highly matrix organization with strong communication, planning, and collaboration skills.
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
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 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/ (https://careers.bms.com/eeo-accessibility) 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.
Company: Bristol-Myers Squibb
Req Number: R1584990
Updated: 2024-11-11 04:13:25.601 UTC
Location: Princeton-NJ
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
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 .
Position Summary:
Accountable for implementing and supporting strategic information systems that enable Global Development Operations (GDO), specifically focusing on Veeva Clinical Vault (Veeva CTMS, Veeva eTMF). This role, under the supervision of the Veeva Engineering Lead, will be responsible for identifying, designing, and developing solutions to meet the continuous demand within GDO-IT, as well as managing the build and run of these technology assets, ensuring they are reliable, accessible, & secure.
Specific responsibilities:
+ Partner with GDO-IT Engineering Leads and IT Product Managers to plan, prioritize, deliver & support strategic digital capabilities and ensure maximum value is achieved.
+ Support Veeva Engineering lead in collaborating with the GDO-IT product teams and assist in identifying, designing, and developing technical solutions to meet business demand
+ Manage the build and run of technology assets.
+ Assist with technical work related to data quality issues, data correction, data load, etc.
+ Provide Audit/ Inspection support
+ Provide L2/L3 support for Veeva CTMS and eTMF application for time sensitive support tickets
+ Work with the vendor for any major issues/bugs in the applications
+ Understand the integrations thoroughly and work with the integrated teams (internal & external) for any issues.
+ Drive process optimization to bring efficiency
Requirements:
+ Must have a minimum of 6 years of related work experience in a Biopharmaceutical environment.
+ BS/BA in Engineering, Computer Science or Life Sciences (or other quantitative related discipline).
+ Must have Veeva Clinical Vault expertise, with specific knowledge of Veeva CTMS and eTMF.
+ Must have broad technology expertise, good working knowledge of Pharmaceutical R&D business processes, particularly in Clinical Trial Operations, with demonstrated command of key concepts, systems and processes.
+ Preferred - certified in Veeva Vault Administration
+ Preferred to have experience / understanding of GxP validation SDLC process.
+ Demonstrated competency in execution of multiple large projects simultaneously within a Product Model leveraging Agile methods.
+ Critical thinking to investigate issues with systems and data, and identify solutions for short-term remediation and long-term strategy.
+ Experience in evaluating new technologies, delivery methods (e.g., SaaS/PaaS/IaaS), and services, and contributing towards the design and implementation of those new solutions.
+ Ability to achieve successful consensus among differing priorities and stakeholders in both the IT and Business communities.
+ Must be a relationship builder and capable of working effectively in a highly matrix organization with strong communication, planning, and collaboration skills.
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
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 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/ (https://careers.bms.com/eeo-accessibility) 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.
Company: Bristol-Myers Squibb
Req Number: R1584990
Updated: 2024-11-11 04:13:25.601 UTC
Location: Princeton-NJ
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
Source : Bristol Myers Squibb
