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Real World Evidence Rwe Jobs in New York (NOW HIRING)

Parexel

Senior RWE/RWA Programmer

New Brunswick, NJ · On-site +1

Parexel is seeking a Senior Real-World Evidence (RWE) Analyst Programmer Join a high-impact team as a remote Sr. Real-World Evidence Analyst Programmer , supporting innovative work across Canada or ...

TechData Service Company LLC

Be Seen First

RWE/RWD Statistical Analyst(Remote)

Basking Ridge, NJ · Remote

$100K - $145K/yr

TechData is looking for Real World Evidence (RWE) statistical analysts. Please see below requirements. TechData offers very competitive and best pay rate and benefits. Position Summary The RWE ...

Jj

Director HTA Statistics & RWE Methods

Raritan, NJ

$164 - $282.90/hr

... 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 ...

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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 New York? The most popular types of Real World Evidence Rwe jobs in New York are:
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What job categories do people searching Real World Evidence Rwe jobs in New York look for? The top searched job categories for Real World Evidence Rwe jobs in New York are:
What cities in New York are hiring for Real World Evidence Rwe jobs? Cities in New York with the most Real World Evidence Rwe job openings:
Real World Evidence Rwe jobs near you
Infographic showing various Real World Evidence Rwe job openings in New York as of July 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution.
Director, Global Real World Evidence (RWE)

Director, Global Real World Evidence (RWE)

Johnson & Johnson

Raritan, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 16 days ago

Johnson & Johnson rating

8.2

Company rating: 8.2 out of 10

Based on 110 frontline employees who took The Breakroom Quiz

31st of 86 rated pharmaceutical

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Data Analytics & Computational Sciences

Job Sub Function:

Data Science

Job Category:

People Leader

All Job Posting Locations:

Raritan, New Jersey, United States of America

Job Description:

We are searching for the best talent for Director, Global Real World Evidence (RWE).

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

Purpose:

TheDirector of GlobalReal-world Evidence (RWE)isa stretegic leadership role within theGlobal Medical Affairs organization,supporting enterprise and therapeutic area priorities through the development and execution of innovative global RWE strategies.Thisroleworksin close partnershipacross theGlobalCommercial Strategy Organization(GCSO)to generate integrated evidence thatenhancesglobal go-to-market launch planning by making innovative and strategic decisions and investments based on RWE insights.

The role focuses on leveraging deep industry knowledge and cross-functional insights to identify opportunities for RWE growth both within GCSO and beyond, and implementing effective strategies into action. Collaboration is essential across global medical affairs, market access, commercial teams, and partners outside of GCSO, such as regional medical affairs, commercial groups, US Real World Value & Evidence (RWV&E), Global Epidemiology, J&J Technology (JJT) Data Sciences, and R&D Data Science, among others. The Director of Global RWE ensures these efforts align with stakeholder strategies at regional and local levels and provides support for implementation when needed.

You will be responsible for:

  • Lead global RWE strategy and execution for key immunology assets, including define research questions, develop study protocols, study design/methodology, real-world data selection and analysis, results dissemination, and communication to support medical adoption and product differentiation across regions.

  • Serve as the Global RWE representative on cross-functional franchise teams, partnering closely with Global Medical Affairs, Market Access, and other stakeholders. Act as the RWE subject matter expert in Global Integrated Evidence Generation Plan (IEGP) and oversee global real-world data and evidence generation strategies.

  • Advance RWE capabilities and best practices by sharing latest development and guidance in RWE, delivering technical training, strengthening internal expertise in advanced RWE methods, and supporting governance, quality standards, and compliance for global and local RWE activities.

  • Lead Evidence Lab coordination to drive concept development, stakeholder alignment, and prioritization of RWE opportunities within the Global IEGP process.

  • Ensure full compliance with regulatory, legal, and commercial regulations in research conduct, data usage, and scientific communication.

Qualifications / Requirements:

Required Skills:

  • Master's degree in a quantitative field (e.g., epidemiology, HEOR, pharmacoepidemiology, biostatistics); PhD preferred

  • Minimum of 6 years of relevant experience in pharma, biotech, or healthcare consulting.

  • Demonstrated expertise in observational research (prospective and retrospective) across study design, conduct, analysis, and reporting.

  • Experience executing RWE studies using diverse real-world data sources, multi-country RWE experience preferred.

  • Understanding of global healthcare delivery, reimbursement, and payer dynamics desirable.

  • Strong communication, storytelling, and presentation skills, with ability to translate complex methods and statistics for both technical and non-technical stakeholders.

  • Highly motivated, intellectually curious, and skilled at managing multiple priorities in a fast-paced environment.

  • Proven experience working effectively in a matrixed, cross-functional team environment.

  • Proficiency in standard office applications (Word, Excel, PowerPoint) and familiarity with statistical programming tools (SAS, R, Python).

Preferred Skills:

  • Experience in dermatology, rheumatology, gastroenterology, and broader immune mediated inflammatory therapy area

  • Good understanding of evidence-based medicine and comparative effectiveness analyses in healthcare research

  • Experience of managing analytical/statistical activities with external service providers

Other:

  • The position is based in Raritan, NJ and will require up to 15% travel

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource.

Required Skills:

Preferred Skills:

The anticipated base pay range for this position is :

The anticipated base pay range for this position is $164,000 to $282,900 USD.

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Company's long-term incentive program. Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation -120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year Holiday pay, including Floating Holidays -13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child Condolence Leave - 30 days for an immediate family member: 5 days for an extended family member Caregiver Leave - 10 days Volunteer Leave - 4 days Military Spouse Time-Off - 80 hours Additional information can be found through the link below. https://www.careers.jnj.com/employee-benefits

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