招聘
薪酬
PLN 494,649 - PLN 599,203
福利待遇
•Healthcare
•401(k)
•Equity
•Unlimited Pto
•Flexible Hours
•Parental Leave
•Mental Health
必备技能
SAS
Programming
Statistical Analysis
Data Management
CDISC Standards
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.
- Senior Programmers
- Starszy Programista provide comprehensive programming expertise to clinical project teams to support the development, regulatory approval and market acceptance of Bristol Myers Squibb (BMS) products. This position is primarily responsible for the design, development and implementation of technical solutions for integrating, analyzing and reporting clinical data. Managers of Statistical Programming develop collaborative relationships and work effectively within Global Biometrics & Data Sciences (GBDS), with external vendors and members of cross-functional development teams.
Responsibilities:
-
Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures; Perform programming validation to ensure quality of analysis datasets and programming outputs
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Provides comprehensive programming support for project teams, including development of programming strategies, standards, specifications and programmed analysis
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Support the electronic submission preparation and review
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Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements; Assesses impact on programming activities
-
Interacts with vendors regarding project standards, programming conventions, programming specifications and file transfers
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Provides leadership for ensuring quality of Global Biometric and Data Sciences (GBDS) deliverables by consistently applying standards and complying with regulatory requirements, guidance and corporate and departmental SOPs and work practices
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Identifies opportunities for increased efficiency and consistency within GBDS and our interactions with strategic vendors
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Independently leads and / or performs programming assignments across multiple projects with minimal supervision
-
Support improvement initiatives
Minimum Requirements:
-
Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required.
-
At least 4 years programming experience in industry.
-
Demonstrated proficiency in using SAS, R or other programming languages to produce derived analysis datasets and TFLs.
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Have in-depth understanding of clinical data structure (e.g. CDISC standards) and relational database.
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Demonstrated skills in using software tools and applications, e.g., MS office, XML, Pinnacle 21.
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Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM.
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Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission.
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Have good understanding of regulatory, industry, and technology standards and requirements.
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Have good knowledge of statistical terminology, clinical tests, medical terminology and protocol designs.
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Demonstrated ability to work in a team environment with clinical team members.
Preferred Requirements:
-
Minimum of 4 years clinical / statistical programming experience within pharmaceutical clinical development
-
Supporting regulatory filings (e.g. NDA, BLA, MAA)
-
Knowledge of the drug development process, clinical trial methodology, statistics and familiarity with global regulatory requirements
-
Experience in other software packages (e.g. R)
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Experience with the Linux operating system
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.
Compensation Overview:
- Warsaw
- PL: zł237,830 - zł288,194
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 employee’s 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 adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility 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: https://careers.bms.com/california-residents/
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.
Any 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 TAEnablement@bms.com. 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.
- R1597354 : Senior Programmer
- Manager, Statistical Programming
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关于Bristol-Myers Squibb

Bristol-Myers Squibb
PublicBristol-Myers Squibb engages in the discovery, development, licensing, manufacturing, marketing, distribution and sale of pharmaceuticals.
10,001+
员工数
New York
总部位置
$150B
企业估值
评价
4.0
10条评价
工作生活平衡
3.2
薪酬
4.1
企业文化
4.0
职业发展
3.4
管理层
3.5
75%
推荐给朋友
优点
Great benefits and competitive compensation
Supportive management and good team dynamics
Flexible working hours and remote work options
缺点
Heavy workload and high pressure
Long working hours during peak seasons
Limited career advancement opportunities
薪资范围
2,115个数据点
Junior/L3
Mid/L4
Senior/L5
Director
Junior/L3 · Business Analyst
0份报告
$22,000
年薪总额
基本工资
-
股票
-
奖金
-
$18,700
$25,300
面试经验
3次面试
难度
3.0
/ 5
时长
14-28周
面试流程
1
Application Review
2
Recruiter Screen
3
Technical Phone Screen
4
Hiring Manager Interview
5
Panel Interview
6
Offer
常见问题
Technical Knowledge
Behavioral/STAR
Past Experience
Culture Fit
Problem Solving
新闻动态
Bristol Myers Squibb Company $BMY Shares Purchased by Merit Financial Group LLC - MarketBeat
MarketBeat
News
·
3d ago
Assetmark Inc. Lowers Stock Position in Bristol Myers Squibb Company $BMY - MarketBeat
MarketBeat
News
·
3d ago
Bristol Myers Squibb to cut 206 more jobs in New Jersey (updated) - NJBIZ
NJBIZ
News
·
3d ago
FDA Approves Sotyktu From Bristol Myers Squibb - Pharmacy Times
Pharmacy Times
News
·
4d ago