Collaborate with BI&T partners, clinical study teams, Clinical trial analysts, trial managers, clinical operations leads, domain experts, and cross-functional leaders in data engineering, data ...
Collaborate with BI&T partners, clinical study teams, Clinical trial analysts, trial managers, clinical operations leads, domain experts, and cross-functional leaders in data engineering, data ...
Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. * Ensure data accuracy, completeness ...
Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. * Ensure data accuracy, completeness ...
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
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Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
New
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
New
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
New
Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. * Ensure data accuracy, completeness ...
Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. * Ensure data accuracy, completeness ...
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
New
Quick apply
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
New
Clinical Trial Manager
Princeton, NJ · Remote
As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... Support the operational strategy related to assigned vendors, data flow, drug supply, remote ...
Clinical Trial Manager
Princeton, NJ · Remote
As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... Support the operational strategy related to assigned vendors, data flow, drug supply, remote ...
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
Clinical Trial Manager
San Diego, CA · Remote
$110K - $140K/yr
Description The Clinical Trials Manager (CTM) will support the conduct of clinical trials and data collection and review, monitoring adherence to protocols, and all activities related to trial ...
Clinical Trial Manager
San Diego, CA · Remote
$110K - $140K/yr
Description The Clinical Trials Manager (CTM) will support the conduct of clinical trials and data collection and review, monitoring adherence to protocols, and all activities related to trial ...
Clinical Trial Manager/Senior Clinical Trial Manager
Waltham, MA · Hybrid
$161K - $187K/yr
Clinical Trial Manager/Senior Clinical Trial Manager Location: Hybrid 3 days/week if located near ... Successfully interface with Data Management, Biostatistics and Clinical Development to ensure ...
Clinical Trial Manager/Senior Clinical Trial Manager
Waltham, MA · Hybrid
$161K - $187K/yr
Clinical Trial Manager/Senior Clinical Trial Manager Location: Hybrid 3 days/week if located near ... Successfully interface with Data Management, Biostatistics and Clinical Development to ensure ...
Clinical Trial Associate
Newark, CA · On-site
$86K - $105K/yr
The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Perform data verification and reconciliation of study trackers against EDC, CTMS, and other ...
Clinical Trial Associate
Newark, CA · On-site
$86K - $105K/yr
The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Perform data verification and reconciliation of study trackers against EDC, CTMS, and other ...
Clinical Database Analyst
Lexington, MA · On-site
Responsible for visualizing clinical trial data in SPOTFIRE for the Analytical Risk-based Monitoring (ARBM) group and for the medical reviewers in the iDARTs application (an internally developed tool ...
Clinical Database Analyst
Lexington, MA · On-site
Responsible for visualizing clinical trial data in SPOTFIRE for the Analytical Risk-based Monitoring (ARBM) group and for the medical reviewers in the iDARTs application (an internally developed tool ...
Clinical Trial Manager
Watertown, MA · On-site
$138K - $153K/yr
Perform and contribute to clinical data cleaning as part of cross-functional data review team ... Preferred: * Experience with oncology clinical trial management and/or global clinical trials.
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Clinical Trial Manager
Watertown, MA · On-site
$138K - $153K/yr
Perform and contribute to clinical data cleaning as part of cross-functional data review team ... Preferred: * Experience with oncology clinical trial management and/or global clinical trials.
New
Clinical Trial Associate
Needham, MA · On-site
$88K - $100K/yr
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Ensure the quality of data submitted from assigned study tasks and timely data submission ...
Clinical Trial Associate
Needham, MA · On-site
$88K - $100K/yr
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Ensure the quality of data submitted from assigned study tasks and timely data submission ...
Clinical Trial Manager
Morrisville, NC · On-site
The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials ... This includes vendor management, monitoring subject safety and data collection, and ensuring ...
Clinical Trial Manager
Morrisville, NC · On-site
The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials ... This includes vendor management, monitoring subject safety and data collection, and ensuring ...
Clinical Trial Manager/Sr Clinical Trial Manager
San Diego, CA · On-site
$145K - $190K/yr
Participate in data cleaning activities and developing appropriate data outputs. * Understand and ... For Clinical Trial Manager, at least 5 years of relevant experience in oncology clinical operations ...
Clinical Trial Manager/Sr Clinical Trial Manager
San Diego, CA · On-site
$145K - $190K/yr
Participate in data cleaning activities and developing appropriate data outputs. * Understand and ... For Clinical Trial Manager, at least 5 years of relevant experience in oncology clinical operations ...
Clinical Trial Manager/Senior Clinical Trial Manager Location: Hybrid 3 days/week if located near ... Successfully interface with Data Management, Biostatistics and Clinical Development to ensure ...
Clinical Trial Manager/Senior Clinical Trial Manager Location: Hybrid 3 days/week if located near ... Successfully interface with Data Management, Biostatistics and Clinical Development to ensure ...
Clinical Trial Associate/Clinical Research Coordinator
Pittsburgh, PA · On-site
$32.50 - $44.50/hr
Conducting reviews of trial data and follow GCP/ICH protocols/guidelines. Will require travel to Clinical sites, including up to 50% of the time, during peak periods. Primary Responsibilities:
Clinical Trial Associate/Clinical Research Coordinator
Pittsburgh, PA · On-site
$32.50 - $44.50/hr
Conducting reviews of trial data and follow GCP/ICH protocols/guidelines. Will require travel to Clinical sites, including up to 50% of the time, during peak periods. Primary Responsibilities:
Senior Clinical Trial Manager, Oncology
Millbrae, CA · On-site
$143K - $173K/yr
Data Management: Oversee data collection, entry, and validation processes to maintain the integrity of clinical trial data. * Cross-functional Collaboration: Foster effective communication and ...
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Senior Clinical Trial Manager, Oncology
Millbrae, CA · On-site
$143K - $173K/yr
Data Management: Oversee data collection, entry, and validation processes to maintain the integrity of clinical trial data. * Cross-functional Collaboration: Foster effective communication and ...
New
Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines. * Review source documents and medical records to ensure complete and accurate ...
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Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines. * Review source documents and medical records to ensure complete and accurate ...
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Clinical Trial Data information
See salary details
$11.54 - $16.74
4% of jobs
$16.74 - $21.94
15% of jobs
$24.54 is the 25th percentile. Wages below this are outliers.
$21.94 - $27.14
13% of jobs
$27.14 - $32.34
8% of jobs
The median wage is $35.23 / hr.
$32.34 - $37.54
19% of jobs
$37.54 - $42.74
13% of jobs
$44.83 is the 75th percentile. Wages above this are outliers.
$42.74 - $47.95
10% of jobs
$47.95 - $53.15
5% of jobs
$53.15 - $58.35
11% of jobs
$58.35 - $63.55
1% of jobs
$63.55 - $68.75
1% of jobs
$11
$37
$68
How much do clinical trial data jobs pay per hour?

Senior Manager, Data Engineer, Clinical Operations
Princeton, NJ • On-site
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 3 days ago
Bristol Myers Squibb rating
8.2
Based on 51 frontline employees who took The Breakroom Quiz
34th of 86 rated pharmaceutical
Job description
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 Summary:
As a Senior Manager, Data Engineer, you will play a vital role in supporting the broader Data Engineering community to deliver cutting-edge data and analytics platforms for our Global Drug Development (GDD) Patient & Site engagement and Feasibility & Forecasting domain.
We seek a candidate who excels at creating innovative, reliable, secure, and easy-to-use data ecosystems that support the full data product lifecycle - including ingesting, storing, processing, governing, and interacting with data.
You will collaborate closely with BI&T partners, business analysts, and data engineers, as well as Clinical Operations specialists, Trial Management professionals, and other domain experts to support various data-driven initiatives and enhance the overall BMS data ecosystem. Additionally, you will be expected to leverage Generative AI (GenAI), Databricks, and semantic technologies to drive innovation and efficiency within our data platforms.
Key Responsibilities:
- Support and contribute to cross-functional teams for all AI and Data initiatives across Clinical Trial Operations product lines, helping drive critical programs forward in a lean, high-impact environment.
- Develop and enhance data solutions to accelerate data usage across clinical R&D, ensuring robustness, interoperability with consumer applications, and scalability.
- Collaborate with BI&T partners, clinical study teams, Clinical trial analysts, trial managers, clinical operations leads, domain experts, and cross-functional leaders in data engineering, data product teams, and data operations to support effective adoption of our Data Platform.
- Partner with business and data product owners to deliver solutions for data product development, standardization, testing, lineage, meeting latency requirements, and ensuring access governance across clinical trial data assets.
- Optimize the data platform for performance, scalability, interoperability, availability, and cost-effectiveness using techniques such as cloud-native parallel processing, Databricks Delta Lake, caching, and partitioning.
- Utilize Databricks Unity Catalog to enforce data governance, manage metadata, and ensure end-to-end data lineage across clinical trial data products.
- Contribute to the development of self-service data discovery solutions, fostering findability, accessibility, and reusability of clinical trial operational data assets.
- Maintain documentation of processes, structures, and knowledge sharing; deliver strong technical recommendations and execute solutions effectively across the enterprise.
- Build and deploy GenAI-powered and NLP-driven applications that deliver measurable outcomes across clinical trial operations, including efficiency gains, trial timeline acceleration, risk mitigation, and compliance automation.
- Collaborate with data product owners, engineers, and data scientists to develop and operationalize cloud-based GenAI and LLM-powered applications, utilizing techniques such as RAG, fine-tuning, and vector embeddings to deliver high-quality data discovery and consumption features for clinical operations workflows.
- Stay current on technology trends in GenAI, RAG, semantic search, Databricks, cloud orchestration, and containerization; apply emerging best practices to optimize platform performance, scalability, and cost-effectiveness.
- Provide guidance and mentorship to junior analysts, interns, and vendor resources on Databricks, technical best practices, and business alignment, fostering a culture of continuous learning and improvement.
Qualifications & Experience:
- 7+ years of cross-domain experience in Data Engineering, Analytics, and AI/ML, with proven hands-on experience implementing and operating data capabilities and solutions in a cloud environment.
- Strong stakeholder engagement and communication skills; ability to influence and drive adoption of data solutions across functional teams.
- Domain knowledge across Clinical Trail Delivery, including feasibility, site selection, forecasting and trial execution is a strong plus.
- Hands-on expertise with Databricks, including Delta Lake, Unity Catalog, Databricks Workflows, Mosaic AI, and MLflow; Databricks certification (e.g., Databricks Certified Data Engineer Associate/Professional) is a strong plus.
- Demonstrated expertise in cloud-native data platforms, ETL/ELT pipeline design, data modeling, and semantic analytics for large-scale, complex datasets, with hands-on DevOps experience.
- Strong proficiency in Python, SQL, Spark (including PySpark on Databricks), and GenAI frameworks; hands-on experience with LLM architectures, RAG, prompt engineering, and agentic frameworks.
- Proficiency in creating and maintaining optimal data pipeline architecture for large, complex datasets, including semantic modeling within a domain - preferably life sciences or clinical trial operations.
- Demonstrated experience delivering production-grade GenAI applications, predictive models, and self-service analytics tools supporting critical clinical business functions.
- Working knowledge of LLM and GenAI-driven approaches, including RAG, Chain-of-Thought, fine-tuning, vectorization, agentic frameworks, and prompt engineering techniques for improving the accuracy of LLM-based responses.
- Commitment to engineering excellence, documentation, and process improvement; functional knowledge of Life Sciences R&D and clinical trial operations is highly preferred.
- Familiarity with clinical trial management systems (e.g., Veeva Vault, Medidata Rave, IRT) and their underlying data structures.
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:
Princeton - NJ - US: $153,770 - $186,327
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 rate 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. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
- Health Coverage: Medical, pharmacy, dental, and vision care.
- Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
- Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work-life benefits include:
Paid Time Off
- US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
- Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
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.
R1604108 : Senior Manager, Data Engineer, Clinical Operations
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About Bristol-Myers Squibb
Sourced by ZipRecruiter
Bristol-Myers Squibb is a world-renowned global Biopharmaceutical company headquartered in New York, NY, US. Established in 1887, the company has more than 130 years’ worth of history dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. The company operates in the healthcare industry and thrives on providing a range of pharmaceutical products and services for various medical fields, like oncology, cardiovascular diseases, and immunoscience. Notably, Bristol-Myers Squibb is known for its commitment to relentless research and innovative drug development, which has led to breakthroughs like Opdivo, one of the first immunotherapies.
Industry
Scientific research and development services and pharmaceutical and medicine manufacturing
Company size
10,000+ Employees
Headquarters location
New York, NY, US