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Home Based Rwe Jobs (NOW HIRING)

Photocure

Medical Operations Manager - NA

Princeton, NJ · On-site +1

$180K - $210K/yr

... RWE) from bladder cancer patients undergoing treatment. The position will involve both internal and ... U.S. cross-functional team members including field-based counterparts and home office-based ...

Photocure

Medical Operations Manager - NA

Princeton, NJ · On-site

... RWE) from bladder cancer patients undergoing treatment. The position will involve both internal and ... U.S. cross-functional team members including field-based counterparts and home office-based ...

Alkermes

Associate Director, HEOR

Waltham, MA · On-site

$179K - $205K/yr

... world evidence (RWE), health economic models and assessments, payer value communications ... Exact compensation may vary based on skills, training, knowledge, and experience. Alkermes offers a ...

Alkermes

Associate Director, HEOR

Waltham, MA · Hybrid

$179K - $205K/yr

... world evidence (RWE), health economic models and assessments, payer value communications ... home. This position is eligible for the hybrid workplace model, requiring work to be completed ...

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Home Based Rwe information

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How much do home based rwe jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for home based rwe in the United States is $23.97, according to ZipRecruiter salary data. Most workers in this role earn between $15.38 and $31.01 per hour, depending on experience, location, and employer.

What is a home based RWE job?

Home-based RWE (Real World Evidence) jobs involve analyzing and interpreting health data outside of traditional clinical trials, often from sources such as electronic health records, insurance claims, and patient registries. Professionals in these roles work remotely to generate insights that inform healthcare decisions, support regulatory submissions, and guide product development. These positions typically require strong analytical skills, experience in epidemiology or biostatistics, and familiarity with healthcare data sources.

How does working as a home based Real World Evidence (RWE) professional differ from onsite roles in collaboration and communication?

As a Home-Based RWE professional, you will primarily collaborate virtually with cross-functional teams such as clinical researchers, data scientists, and regulatory affairs staff. Effective digital communication skills are vital, as much of the coordination occurs through video calls, project management tools, and shared digital platforms. While you have the flexibility of remote work, maintaining regular touchpoints and clear documentation is essential to stay aligned with project goals and timelines. You may also participate in virtual team meetings and occasional in-person workshops or conferences, depending on the employer.

What are the key skills and qualifications needed to thrive as a home based Real World Evidence (RWE) analyst?

To thrive as a Home-Based RWE Analyst, you need a solid background in epidemiology, biostatistics, or related health sciences, often supported by a relevant degree. Familiarity with statistical software (such as SAS, R, or Python), data management systems, and experience with real-world data sources like electronic health records are typically required. Strong analytical thinking, attention to detail, and effective communication are essential soft skills for interpreting data and presenting findings to stakeholders. These skills ensure accurate analysis, meaningful insights, and effective collaboration in remote environments, driving evidence-based decisions in healthcare.

What is the difference between Home Based Rwe vs Home Based Rwe?

AspectHome Based Rwe

Since the comparison is with itself, the differences are minimal or non-existent. Typically, 'Home Based Rwe' refers to remote workers conducting real-world evidence (Rwe) research or data collection from home. They usually require similar credentials, such as healthcare or research certifications, and work in the healthcare or pharmaceutical industry. The role involves remote data analysis, patient record review, or research coordination, often with flexible schedules. Overall, 'Home Based Rwe' is a specialized remote role focused on real-world evidence activities within the healthcare sector.

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Home Based Rwe jobs near you
Infographic showing various Home Based Rwe job openings in the United States as of September 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 25% In-person, and 75% Remote job distribution, with an average salary of $49,864 per year, or $24 per hour.

Medical Operations Manager - NA

Princeton, NJ • On-site, Remote

Photocure
See more jobs at Photocureexternal

$180K - $210K/yr

Full-time

Posted 20 days ago

Key responsibilities

  • Oversee operational support and implementation of research studies, including clinical development and post-approval studies.

  • Manage external vendors, monitor data quality, and ensure compliance with registry requirements and study protocols.

  • Support publication activities and medical data dissemination to internal and external stakeholders.

Job description

The Medical Operations Manager is a cross functional role responsible for operational support and implementation of research studies and other relevant associated activities at Photocure in the North American region (US/Canada). This hybrid role includes operational oversite of projects in clinical development as well as post-approval studies at Photocure, in particular, the U.S. Cysview Blue Light Cystoscopy Registry, a large multi-center study collecting Real-World Evidence (RWE) from bladder cancer patients undergoing treatment.

The position will involve both internal and external stakeholder interactions. Relevant stakeholders include third party vendors such as CROs, study site IRB and contract professionals, as well as interface with Finance and Legal personnel.

This position reports directly to the VP of North America Medical & Clinical Affairs.

Specific Responsibilities and Activities include:

  • Act as the primary point of contact for operational stewardship and oversight of the research projects including sponsored studies, the U.S. Cysview Registry and IITs (Investigator Initiated Trials).
  • Oversee and provide input to the development and/or improvement of study specific documentation including case report forms (CRF), data management plan, and monitoring plan.
  • Manage external contacts, ensuring the CROs and Third-Party Vendors (EDC, CRO, etc.) are in alignment and are delivering per the scope of work.
  • Review of anonymized data in the electronic data capture system to monitor data entered into the Registry, research projects and ensure completeness and quality.
  • Confirm compliance with the clinical trial registry requirements (updates to Clinicaltrial.gov, SOPs, etc.) including oversight and execution of study audits as needed.
  • Oversee and assist Finance in data reconciliations of Registry invoicing.
  • Work with Finance to provide input into budget needs and development/management costs.
  • Operational support while onboarding new sites/study initiation.
  • Interact with external and internal Legal entities to discuss site contracts/amendments.
  • Leads risk assessment and identifies risk mitigation strategies at the study level.
  • Execution of the clinical study against planned timelines, deliverables and budget.

Publications & Evidence Dissemination Support:


  • Assist in medical communication and data dissemination
  • Contribute to operations related to publication strategy, including abstracts, manuscripts, and presentations at scientific congresses (e.g., AUA, EAU)
  • Provide dissemination of clinical data internal stakeholders timely
  • Align with Photocure Global Medical Affairs on topics (e.g. publication communications)

Core Competencies / Knowledge & Skill Requirements


  • Ability to drive process improvement initiatives in concert with our clinical collaborators.
  • Ability to understand and implement the operational strategic direction and guidance for respective clinical studies.
  • Demonstrated vendor management experience.
  • Ability to work independently and execute tasks within deadlines.
  • Ability to work with and support cross functional teams.
  • Must be proactive, self-disciplined, can prioritize. Must be detailed oriented and administratively organized.
  • Experience in clinical study operations including experience developing protocols and key study documents.
  • Has experience and can understand electronic medical records (EMR).
  • Effective project management skills, cross-functional team leadership and organizational skills.
  • Excellent oral and written communication skills.

Education, Experience & Training Required


  • Advanced degree (MD, DO, PharmD, PhD) in life sciences or related field
  • 5-7 years of relevant experience.
  • Experience with RWE required.
  • Previous Urology or Oncology experience ideal.
  • Fully Remote with ability to travel occasionally

Significant Contacts

  • Internal: U.S. cross-functional team members including field-based counterparts and home office-based functions such as Global and NA Medical Affairs, Legal, Regulatory, Biostatistics, Market Access, Finance.
  • External: Investigators, clinical trial sites, CRO's, CRAs, vendors, regulatory authorities, and managed care decision



Salary range for this position is from $180,000-$210,000 depending on candidate's experience, educational background and geographic location. This role is eligible for a bonus and company benefits.

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