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Real World Evidence Rwe Jobs in Inkster, MI (NOW HIRING)

Our AI-powered Tutor Copilot enhances your sessions with real-time instructional support, lesson ... World Wars, Cold War, and European integration. Ability to explain political, economic, social, and ...

AP European History Tutor

Detroit, MI · Remote

$18 - $40/hr

Our AI-powered Tutor Copilot enhances your sessions with real-time instructional support, lesson ... World Wars, Cold War, and European integration. Ability to explain political, economic, social, and ...

... in evidence. Join us and use your analytical expertise to shape how the world connects with our ... real-time streaming experiences. You aren't just a software engineer; you are an AI Orchestrator ...

We have strong evidence that in-system relationship-building dramatically amplifies the performance ... Build and iterate on the SAM playbook - Identify what's working in real time and feed it back into ...

Do you believe data tells the real story? We do! Redefining mobility requires quality data, metrics ... Join us and use your data expertise and analytical skills to drive evidence-based, timely decision ...

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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 cities near Inkster, MI are hiring for Real World Evidence Rwe jobs? Cities near Inkster, MI with the most Real World Evidence Rwe job openings:
V&V Vehicle Testing Supervisor

V&V Vehicle Testing Supervisor

Ford Motor Company

Dearborn, MI • Hybrid

$115K - $218K/yr

Full-time

Medical, Dental, Vision, Life, PTO

Posted 29 days ago


Job description

Ford's Electric Vehicles, Digital and Design (EVDD) team is charged with delivering the company's vision of a fully electric transportation future. EVDD is customer-obsessed, entrepreneurial, and data-driven and is dedicated to delivering industry-leading customer experience for electric vehicle buyers and owners. You'll join an agile team of doers pioneering our EV future by working collaboratively, staying focused on only what matters, and delivering excellence day in and day out. Join us to make positive changes by helping build a better world where every person is free to move and pursue their dreams.

This position... 

  • Leads the Software Vehicle Validation team to deliver vehiclelevel software validation across Full DV, Mini DV, and UAT to meet GPDS milestones and FAP expectations. 

  • Owns validation strategy and execution planning, ensures traceable/auditable test evidence, drives early defect discovery and defectescape reduction through crossfunctional triage, and provides readiness assessments for gate/release decisions. 

  • Builds team capability through training, standard work, coaching, and reports results and KPIs to drive continuous improvement while ensuring compliance and governance.

You'll have...

  • Bachelor's degree in Computer Science, Computer Engineering, Systems Engineering or related field

  • 7+ years of vehicle testing experience, with the following experience including software

  • 2+ years of experience with standards and regulations Functional Safety (ISO26262)

  • Ability to effectively manage cross-team capabilities and contribute to your peers' success

  • Strong understanding of Agile methodologies, Jira task management, and ALM test management

  • Clear communication

Even better, you may have...

  • Master's degree in Computer Science, Computer Engineering, Systems Engineering or related field

  • Automotive Industry, OEM or consulting experience

  • 2+ years of experience with standards and regulations FMVSS

  • 2+ years of experience with people management and SOW management

You may not check every box, or your experience may look a little different from what we've outlined, but if you think you can bring value to Ford Motor Company, we encourage you to apply!

As an established global company, we offer the benefit of choice. You can choose what your Ford future will look like: will your story span the globe, or keep you close to home? Will your career be a deep dive into what you love, or a series of new teams and new skills? Will you be a leader, a changemaker, a technical expert, a culture builder...or all of the above? No matter what you choose, we offer a work life that works for you, including:

Immediate medical, dental, vision and prescription drug coverage

Flexible family care days, paid parental leave, new parent ramp-up programs, subsidized back-up child care and more

Family building benefits including adoption and surrogacy expense reimbursement, fertility treatments, and more

Vehicle discount program for employees and family members and management leases

Tuition assistance

Established and active employee resource groups

Paid time off for individual and team community service 

A generous schedule of paid holidays, including the week between Christmas and New Year's Day 

Paid time off and the option to purchase additional vacation time. 

This position is leadership level 6 and ranges from $115,500-$218,100.     

Final determination of salary grade will be based on candidate's skills and experience, and base salary will be set within the applicable range according to job scope, responsibility and competitive market value.

For more information on salary and benefits, click here: https://fordcareers.co/LL6

Visa sponsorship is not available for this position.

Candidates for positions with Ford Motor Company must be legally authorized to work in the United States. Verification of employment eligibility will be required at the time of hire.

We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, age, sex, national origin, sexual orientation, gender identity, disability status or protected veteran status. In the United States, if you need a reasonable accommodation for the online application process due to a disability, please call 1-888-336-0660.

This position is hybrid. Candidates who are in commuting distance to a Ford hub location may be required to be onsite four or more days per week. #LI-Hybrid

   #LI-MG3

What you'll do...

1. Vehicle Level Validation Strategy (DV + UAT)

  • Define and own the vehicle level validation strategy across Full DV, Mini DV, and UAT

  • Full DV - complete requirement-based validation for GPDS milestones

  • Mini DV - targeted validation for changes, fixes, and interim releases

  • UAT - customer centric, end to end validation of real-world journeys

  • Align plans to GPDS milestones and CVS quality objectives

  • Partner with Feature Assurance (FA) to define test plans, coverage expectations, and FAP aligned acceptance criteria

2. Full DV & Mini DV Execution (Requirement Based Testing for GPDS)

  • Lead Full DV planning/execution to demonstrate requirements coverage before major GPDS milestones

  • Set Mini DV scope/criteria to validate changes and fixes without rerunning Full DV unnecessarily

  • Ensure traceable, auditable evidence (requirements tests results defects)

  • Provide DV readiness assessments for signoff

3. User Acceptance Testing (UAT) for Customer Quality

  • Make UAT a core validation pillar alongside Full DV and Mini DV

  • Validate customer critical workflows, end to end behavior, and real-world usability expectations

  • Coordinate UAT on vehicles/fleets and include results in FAP ready milestone evidence

  • Use UAT findings as leading indicators of customer impacting risk

4. Defect Escape Reduction & Quality Ownership

  • Drive early defect discovery through balanced Full DV, Mini DV, and UAT execution

  • Lead defect triage with Feature Assurance and feature teams, prioritizing requirement violations and customer impact

  • Track defect aging/closure and escape trends across GPDS milestones

  • Drive prevent recurrence actions for systemic vehicle test gaps

5. Test Planning, Readiness & Cross Functional Alignment

  • Lead integrated vehicle test planning and execution cadence across programs

  • Coordinate readiness for vehicles/fleets, software builds/configurations, and tools/environments (accounts, data, logging)

  • Serve as the vehicle validation interface to Feature Assurance, Feature Systems Engineering, labs, and fleet operations

6. Team Leadership, Training & Capability Development

  • Manage and develop validation teams (vehicle test, DV, and UAT) with clear roles, cadence, and performance expectations

  • Train teams on requirement-based testing, scenario driven UAT, and FAP/GPDS readiness expectations

  • Coach and continuously improve team execution through standard work and feedback

7. Metrics, Reporting & Continuous Improvement

  • Report out test results and KPIs aligned to CVS (DV progress/coverage, UAT trends, defect leakage/escapes, retest efficiency)

  • Use metrics to drive continuous improvement in tools and standard work

8. Governance, Compliance & Standard Work

  • Ensure validation complies with safety, IP, and prototype handling requirements

  • Deliver audit ready validation evidence for GPDS and FAP reviews

  • Own validation standard work, lessons learned, and prevent recurrence documentation


Ford logo

About Ford

Sourced by ZipRecruiter

At Ford Motor Company, we believe freedom of movement drives human progress. With our incredible plans for the future of mobility, we have a wide variety of opportunities for you to accelerate your career and help us define tomorrow's transportation.

Industry

Civil engineering construction

Company size

51 - 200 Employees

Headquarters location

Doral, FL, US

Year founded

1982