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Real World Evidence Rwe Jobs in Basking Ridge, NJ

Learn more at Associate Director, Market Access Analytics and Real World Evidence (MAA & RWE) - Indirect Treatment Comparisons The Associate Director, Market Access Analytics and Real-World Evidence ...

... real-world evidence (RWE). The role spans all therapeutic areas and supports key innovative medicines across the lifecycle, from early development through launch and post-launch. Major Duties ...

... real-world evidence (RWE). The role spans all therapeutic areas and supports key innovative medicines across the lifecycle, from early development through launch and post-launch. Major Duties ...

Staff Data Engineer- RWE

New York, NY · On-site

$170K - $190K/yr

WHAT YOU'LL DO AT H1 As a Staff Data Engineer on the Real World Evidence (RWE) team, you'll be one of the most senior individual contributors and a key technical leader for our largest datasets and ...

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Real World Evidence Rwe information

What is the difference between Real World Evidence Rwe vs Clinical Data Analyst?

AspectReal World Evidence RweClinical Data Analyst
Required credentialsTypically requires a background in healthcare, epidemiology, or biostatistics, often with a master's or PhDUsually requires a degree in health informatics, biostatistics, or related fields, with similar certifications
Work environmentPrimarily in healthcare, pharmaceutical, or research organizations analyzing real-world dataIn clinical research settings, hospitals, or pharmaceutical companies analyzing clinical trial data
Employer and industry usageUsed by pharma companies, healthcare providers, and research institutions to generate real-world insightsUsed by research organizations, hospitals, and pharma for clinical trial data management and analysis

Real World Evidence Rwe professionals focus on analyzing data from real-world settings like electronic health records and insurance claims, while Clinical Data Analysts primarily work with clinical trial data. Both roles require strong analytical skills and related credentials, but Rwe specialists emphasize real-world data sources to inform healthcare decisions.

What jobs are there in clinical trials?

Jobs in clinical trials include Clinical Research Coordinators, Clinical Data Managers, Clinical Research Associates, and Study Monitors. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically in hospitals, research centers, or pharmaceutical companies, with schedules varying from standard to flexible hours.

What is RCT and RWE?

In the context of a Real World Evidence (RWE) role, RCTs (Randomized Controlled Trials) are clinical studies that randomly assign participants to different treatments to assess efficacy, while RWE involves analyzing data from real-world settings like electronic health records and insurance claims to evaluate treatment effectiveness outside controlled trials. Both are important for informing healthcare decisions and regulatory approvals, with RWE complementing RCT data by providing insights from everyday clinical practice.

What is Real World Evidence (RWE) in the healthcare industry?

Real World Evidence (RWE) refers to clinical evidence regarding the usage and potential benefits or risks of a medical product, derived from analysis of real-world data (RWD). This data is collected from sources outside of traditional clinical trials, such as electronic health records, insurance claims, patient registries, and wearable devices. RWE plays a crucial role in understanding how treatments work in routine clinical practice, informing regulatory decisions, and supporting drug development and market access. Organizations use RWE to complement clinical trial data, improving healthcare outcomes and patient care.

What are the roles in clinical trials?

In clinical trials, roles include Principal Investigator who oversees the study, Study Coordinators who manage daily operations, Data Managers who handle data collection and analysis, and Regulatory Affairs Specialists who ensure compliance with regulations. These roles require specific skills, certifications, and knowledge of Good Clinical Practice (GCP) guidelines to ensure the trial's integrity and participant safety.

What are the key skills and qualifications needed to thrive as a Real World Evidence (RWE) professional, and why are they important?

To thrive as a Real World Evidence (RWE) professional, you need a strong background in epidemiology, biostatistics, and data analysis, often supported by an advanced degree in a relevant scientific field. Familiarity with statistical software (such as SAS, R, or Python), real-world data sources (like EHRs and claims databases), and regulatory guidelines (FDA/EMA) is essential. Strong communication, problem-solving, and cross-functional collaboration skills help convey complex findings to stakeholders and integrate RWE into decision-making. These competencies are crucial for generating credible insights that inform clinical, regulatory, and commercial strategies in the healthcare industry.

How does a Real World Evidence (RWE) professional typically collaborate with cross-functional teams in the pharmaceutical industry?

RWE professionals often work closely with colleagues from epidemiology, health economics, medical affairs, and regulatory affairs to design and execute studies using real-world data. Collaboration is essential, as RWE findings support evidence generation for regulatory submissions, market access, and post-marketing surveillance. Regular meetings, data-sharing sessions, and joint project planning are common, ensuring all stakeholders are aligned on study objectives, methodologies, and data interpretation. This collaborative environment helps translate complex data into actionable insights that support decision-making across the organization.

What is RWE in clinical research?

Real World Evidence (RWE) in clinical research refers to data collected from real-world settings outside controlled clinical trials, such as electronic health records, insurance claims, and patient registries. RWE helps researchers and healthcare professionals understand how treatments perform in routine practice and supports decision-making for drug development and regulatory approval.
What are the most commonly searched types of Real World Evidence Rwe jobs in Basking Ridge, NJ? The most popular types of Real World Evidence Rwe jobs in Basking Ridge, NJ are:
What cities near Basking Ridge, NJ are hiring for Real World Evidence Rwe jobs? Cities near Basking Ridge, NJ with the most Real World Evidence Rwe job openings:
Infographic showing various Real World Evidence Rwe job openings in Basking Ridge, NJ as of July 2026, with employment types broken down into 69% Full Time, and 31% Part Time. Highlights an 65% In-person, 17% Hybrid, and 18% Remote job distribution.
Executive Director, Real World Evidence Innovation Center Lead, Global Medical

Executive Director, Real World Evidence Innovation Center Lead, Global Medical

Bristol Myers Squibb

Princeton, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago


Bristol Myers Squibb rating

8.0

Company rating: 8.0 out of 10

Based on 48 frontline employees who took The Breakroom Quiz

37th of 73 rated pharmaceutical


Job description

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.

The Executive Director will serve as thecentral connective nodefor Medical across the BMS enterprise RWE ecosystem - linking Medical study teams to the full landscape of internal and external data assets, technology platforms, AI capabilities, and cross-functional partners. A core priority is working with the Data Analytics and HEOR teams to identifying and integrating the growing portfolio of available therapeutic area-level data sources - including EMR/EHR, claims, registries, specialty datasets, and partner platforms - and making those assets practically accessible and scientifically deployable for the MEG, MAP & RWE and Global Medical teams.

Specifically, the role sits at theintersection of four organizational communities:

MEG study teams- who need scientific guidance, methods support, and database expertise to design and execute high-quality NIS and RWD-integrated studies

Data Analytics & IT / BI&T- who own the data infrastructure, platforms, and tooling that enable RWD acquisition, access, and analysis

External RWD ecosystem- including database vendors, academic partners, and epidemiological networks that the RWDIC will curate and broker access to

Cross Functional Partners including WWTA, HEOR, Clinical Development, Market Access and Commercial teams.

This role is fundamentally acapability-building, connectivity, and enterprise enablement role- not a study execution role. The Executive Director will not own or run RWE studies directly; instead, they will ensure that BMS Medical has the infrastructure, data access, scientific methods, and organizational fluency to generate real-world evidence with speed, rigor, and competitive advantage.

Responsibilities

Build & Lead the RWD Innovation Center

  • Establish this capability within Medical - defining the RWDIC mission, governance model, KPIs, and operating model from the ground up, as an enterprise-level function new to the Medical organization at BMS.

  • Set the strategic vision for how BMS Medical engages with the evolving RWD ecosystem, including new data partnership models, AI-integrated workflows, and enterprise data infrastructure.

  • Serve as theenterprise authority on RWD strategy, data connectivity, and scientific standard acting as a senior resource for Medical leadership and cross-functional partners.

End-to-End Data RWE Capability
  • Build an end-to-end capability which enables Global Medical to lead in the space of RWE generation and publication to meet the needs of HCPs and patients

  • Own the end-to-end data connectivity architecture for Global Medical: mapping, accessing, and mobilizing the full landscape of internal and external data sources available across BMS therapeutic areas.

  • Identify, evaluate, and build an enterprise RWD data landcapeby TA including EMR/EHR systems, claims databases, specialty registries and global sources, ensuring teams know what exists, how to access it, and how to deploy it for their evidence questions.

  • Serve as theorganizational bridge between MEG teams and the Unified Data Layer, ensuring that the data infrastructure investments made in BI&T and Data Analytics are translated into practical, scientific utility for Medical.

  • Drive a culture of continuous innovation to stay ahead of emerging data sources, design paradigms, AI-enabled approaches, and digital tools, and translating them rapidly into practical team capability.

Enterprise Cross-Functional Connectivity & Integration

  • Serve asMedical's senior liaisonto the enterprise RWE ecosystem, actively connecting and aligning with WWTA, HEOR, Clinical Development, Market Access, Commercial, BI&T/Data Analytics to ensure that Medical's RWD capability is integrated within, and benefits from, the broader enterprise infrastructure.

  • Represent Medical's RWD priorities in enterprise technology roadmaps, data governance forums, and AI platform investment decisions, ensuring MEG's scientific requirements shape platform design.

  • Identify and activatedata sources and evidence assets that already exist across BMS TAs, working with BI&T/Data Analytics, HEOR and WWTA to inventory available data, surface reuse opportunities, and prevent duplication of investment.

  • Build and steward enterprise-level partnerships with leading RWD data vendors, academic partners, and epidemiological networks

  • Connect Medical's evidence generation activities to the enterpriseAI and LLM capabilities, ensuring MEG teams are positioned to leverage AI throughout the study lifecycle.

Scientific Expertise: NIS, Epidemiology & Advanced Study Designs

  • Institutionalize RWD as thestandard first step in study planning, ensuring teams interrogate available databases for feasibility, patient population sizing, treatment patterns, and outcome rates before committing to trial infrastructure.

  • Build and maintain the RWDIC knowledge base across the full spectrum of advanced RWD-integrated designs:

    • RWD-informed trials: informing endpoint selection, eligibility criteria, sample size, and increasing probability of technical success

    • External Control Arms: patient matching, propensity methods, eligibility alignment, and regulatory considerations

    • Hybrid designs: integrating RWD with primary data collection, including harmonization and documentation standards

  • Serve as the internal advisor when teams are considering non-traditional designs - pressure-testing feasibility and scientific credibility before resources are committed.

Organizational Capability Building & Training

  • Design and deliver an enterpriseRWD training curriculum- covering database literacy, advanced study designs (ECAs, hybrid, RWD-supplemented trials), AI/digital approaches, and data acquisition pathways - targeted at MEG & MAP study teams.

  • Lead aRWD Community of Practiceand maintain a living knowledge management system - playbooks, database landscape summaries, design guidance, and acquisition process maps - under the RWDIC banner.

  • Build organizational confidence and fluency in RWD within Medical, creating a culture where teams proactively engage available data assets and move with speed and scientific rigor.

Qualifications

  • Degree in Epidemiology, Biostatistics, Health Sciences, or related RWE field (advanced degree PhD or equivalent preferred)

  • 10+ years of progressive experience in real-world evidence, epidemiology, or health data science in a pharmaceutical, biotech, or clinical setting

  • Deep expertise in RWD database ecosystems - including claims, EMR/EHR, registries, and global specialty sources - with proven experience building or managing TA or enterprise-level data access programs

  • Track record of building new functions, teams, or capabilities in large, complex organizations

  • Experience with AI and digital analytics tools applied to RWE workflows

  • Strong executive presence and communication skills - able to represent Medical's data and evidence priorities at the enterprise and leadership level

Locations: Princeton, NJ (preferred); Madison (Giralda Farms), NJ; Uxbridge, UK; Warsaw, Poland; Boudry, Switzerland

#LI-HYBRID

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:

$254,530 - $308,434

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 ...


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About Bristol-Myers Squibb

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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