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Real World Evidence Manager Jobs (NOW HIRING)

The Position The Director, Real World Evidence (RWE) leads the development and execution of RWE for ... S/he manages partner relationships, vendors and strategic collaborations on behalf of CDSE. The ...

The Position The Director, Real World Evidence (RWE) leads the development and execution of RWE for ... S/he manages partner relationships, vendors and strategic collaborations on behalf of CDSE. The ...

The Position The Director, Real World Evidence (RWE) leads the development and execution of RWE for ... S/he manages partner relationships, vendors and strategic collaborations on behalf of CDSE. The ...

Our Real World Evidence team is hiring a Director to lead teams of research professionals ... As a project manager, you will be responsible for ensuring overall quality; develop recommendations ...

Our Real World Evidence team is hiring a Director to lead teams of research professionals ... As a project manager, you will be responsible for ensuring overall quality; develop recommendations ...

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Real World Evidence Manager information

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$23.5K

$133.2K

$227K

How much do real world evidence manager jobs pay per year?

As of Jun 9, 2026, the average yearly pay for real world evidence manager in the United States is $133,228.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,000.00 and $176,000.00 per year, depending on experience, location, and employer.

What is the difference between Real World Evidence Manager vs Data Analyst in the healthcare industry?

AspectReal World Evidence ManagerData Analyst
Required credentialsBachelor's or Master's in Life Sciences, Public Health, or related fields; experience with RWEBachelor's or Master's in Statistics, Mathematics, or related fields; proficiency in data analysis tools
Work environmentPharmaceutical companies, CROs, healthcare organizationsHealthcare providers, research institutions, biotech firms
Employer and industry usageUsed to manage and interpret real-world data for evidence generationUsed to analyze healthcare data for insights and reporting

The Real World Evidence Manager focuses on overseeing the collection and analysis of real-world data to support healthcare decisions, while the Data Analyst primarily interprets healthcare data to generate reports and insights. Both roles require strong analytical skills but differ in their focus on evidence management versus data analysis.

More about Real World Evidence Manager jobs
What cities are hiring for Real World Evidence Manager jobs? Cities with the most Real World Evidence Manager job openings:
What are the most commonly searched types of Real World Evidence jobs? The most popular types of Real World Evidence jobs are:
What states have the most Real World Evidence Manager jobs? States with the most job openings for Real World Evidence Manager jobs include:
Infographic showing various Real World Evidence Manager job openings in the United States as of May 2026, with employment types broken down into 50% Part Time, and 50% Contract. Highlights an 100% Remote job distribution, with an average salary of $133,228 per year, or $64.1 per hour.
Real World Evidence Director

Real World Evidence Director

Novo Nordisk

Plainsboro, NJ

$225K - $300K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago


Novo Nordisk rating

8.4

Company rating: 8.4 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

19th of 71 rated pharmaceutical


Job description

About the Department

The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From healthcare provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved. The one thing that keeps us all marching to the same beat is our patient centered focus. At Novo Nordisk, you will help patients around the world. As their needs evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We're changing lives for a living. Are you ready to make a difference?

The Position

The Director, Real World Evidence (RWE) leads the development and execution of RWE for the assigned therapeutic area or function area through serving as the principal investigator on real world evidence studies. The incumbent acts as a the scientific leader in the coduct of the research in assigned therapeutic area with NNI stakeholders within Clinical, Medical and Regulatory Affairs (CMR), Market Access and Public Affairs, as well as a liaison to therapeutically aligned global counterparts in Epidemiology, Data Science and Real-World Evidence. The Director leads the study team and communicates the RWE project execution to internal and external stakeholders on behalf of RWE study team and USO. S/he manages partner relationships, vendors and strategic collaborations on behalf of CDSE. The Director serves as the lead researcher on the assigned studies within the therapeutic area team or function area. This individual works closely with external experts, vendors and internal functions including medical affairs, biostatistics and data science functions to execute studies.

Relationships

The Director, RWE reports to the Senior Director & TA head in CDSE. The Director is responsible for a cross-functional RWE study team and demonstrates proactive stakeholder engagement and associated RWE execution, communication of RWE studies to internal and external stakeholders, and leadership in the use of appropriate RWE/HEOR methodologies.

Essential Functions

  • RWE study leadership
  • Leads and manages the execution of all RWE assigned within the therapeutic area conducted internally, with partners and with vendors
  • Utilizes the NN Real World Data platform, partnership platforms and analytic tools
  • Develops and maintains stakeholder relationships to ensure optimal utility of RWD within USO
  • Mentors junior staff
  • RWE Communication
  • Communicates the RWE to key internal stakeholders within assigned therapeutic area responsibilities
  • Communicates RWE to customers and scientific community via publication and conferences
  • Leadership in RWE methods
  • Serves as reviewer for the CDSE Protocol Review Committee
  • Acts as a key subject matter expert in various methodological and advanced analytic functions and provides consultation to / collaborates with key internal and external stakeholders directly to provide tangible solutions that are aligned to portfolio strategy

Physical Requirements

10-20% overnight travel required.

Qualifications

  • At least 8-10 years of experience in leading the development of RWE
  • At least 8-10 years of experience in key stakeholder engagement roles
  • Experience in RWE methodologies and advanced analytics
  • Demonstrated prior research accomplishment (e.g., publications in peer-reviewed journals and presentations at scientific conferences)
  • Excellent leadership, strong communication and critical thinking skills with keen knowledge of real-world databases
  • Excellent process and project management skills required including the ability to manage a significant volume of projects with exercise of good triage and judgment skills
  • Keen knowledge and at least 8 years of experience in research using real world data and its applications in clinical and business decision making
  • PhD Preferred or Masters degree in appropriate field required (e.g., epidemiology, biostatistics, health services research, health economics)
  • Strong business acumen and a team player
  • Strong strategic thinking skills

The base compensation range for this position is $225,000 to $300,000. Base compensation is determined based on a number of factors. This position is also eligible for a company bonus based on individual and company performance.  
Novo Nordisk offers long-term incentive compensation and or company vehicles depending on the position's level or other company factors.  
Employees are also eligible to participate in Company employee benefit programs including medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; employee assistance program; tuition reimbursement program; and voluntary benefits such as group legal, critical illness, identity theft protection, pet insurance and auto/home insurance. The Company also offers time off pursuant to its sick time policy, flex-able vacation policy, and parental leave policy. 

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes - we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger - a legacy of impact that reaches far beyond today.

Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.

If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.


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