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Remote Real World Evidence Rwe Jobs in Roslindale, MA

Tempus

Data Architect, Next Platform

Boston, MA · On-site +1

$150K - $200K/yr

Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...

micro1 AI

Cheminformatics Specialist - Remote

Lynn, MA · On-site +1

$90 - $120/hr

Remote micro1 is engaging Computational Biology Experts to contribute their advanced scientific ... Your work will shape how models learn, reason, and perform through high-quality, real-world input.

micro1 AI

Cheminformatics Specialist - Remote

Brockton, MA · On-site +1

$90 - $120/hr

Remote micro1 is engaging Computational Biology Experts to contribute their advanced scientific ... Your work will shape how models learn, reason, and perform through high-quality, real-world input.

micro1 AI

Cheminformatics Specialist - Remote

Boston, MA · On-site +1

$90 - $120/hr

Remote micro1 is engaging Computational Biology Experts to contribute their advanced scientific ... Your work will shape how models learn, reason, and perform through high-quality, real-world input.

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All JobsReal World Evidence Rwe JobsRemote Real World Evidence Rwe JobsRemote Real World Evidence Rwe Jobs in Roslindale, MA

Remote Real World Evidence Rwe information

What is a remote real world evidence RWE professional?

Remote Real World Evidence (RWE) jobs involve gathering, analyzing, and interpreting data from real-world sources—such as electronic health records, insurance claims, patient registries, and wearable devices—to inform healthcare decisions. Professionals in these roles typically work for pharmaceutical companies, research organizations, or healthcare technology firms. Remote RWE jobs allow employees to contribute to research and data analysis from home or other off-site locations, using digital tools to collaborate with teams and stakeholders. These positions are crucial for understanding how medical treatments perform outside of controlled clinical trials, ultimately improving patient care and supporting regulatory submissions.

What are the key skills and qualifications needed to thrive as a remote real world evidence RWE professional?

To thrive as a Remote Real World Evidence (RWE) professional, you need a strong background in epidemiology, biostatistics, or related life sciences, typically supported by an advanced degree (e.g., MPH, MS, PhD). Familiarity with statistical software such as SAS, R, or Python, and experience working with large healthcare databases and electronic health records are crucial. Excellent analytical thinking, problem-solving abilities, and effective communication skills help translate complex data into actionable insights for stakeholders. These competencies ensure the generation of robust, real-world data analyses that inform healthcare decisions and regulatory submissions.

What are some common challenges faced by remote real world evidence RWE professionals and how can they be addressed?

Remote RWE professionals often encounter challenges such as managing large and diverse datasets, ensuring data privacy, and coordinating effectively with cross-functional teams across different time zones. To address these, it's important to have strong data management skills, familiarity with relevant regulations (like GDPR or HIPAA), and effective communication tools. Actively engaging in regular virtual meetings and leveraging collaborative platforms can help maintain alignment with stakeholders and ensure project milestones are met.

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

AspectRemote Real World Evidence RweRemote Data Analyst
Required CredentialsAdvanced degrees in healthcare, epidemiology, or biostatistics; experience with RWE methodologiesBachelor's or master's in data science, statistics, or related fields; proficiency in data analysis tools
Work EnvironmentCollaborates with healthcare providers, pharma companies, and regulatory agencies; focuses on healthcare dataWorks across industries; analyzes large datasets to inform business decisions
Industry UsagePrimarily in healthcare, pharmaceuticals, and regulatory sectorsAcross various sectors including finance, marketing, and healthcare

Remote Real World Evidence Rwe specialists focus on analyzing healthcare data to generate evidence for medical and regulatory decisions, requiring healthcare-specific knowledge. Remote Data Analysts handle diverse datasets across industries, emphasizing data processing and reporting skills. While both roles involve data analysis, RWE roles are more specialized in healthcare and regulatory contexts.

What cities near Roslindale, MA are hiring for Remote Real World Evidence Rwe jobs?

Cities near Roslindale, MA with the most Remote Real World Evidence Rwe job openings:

Remote Real World Evidence Rwe jobs near you
Infographic showing various Remote Real World Evidence Rwe job openings in Roslindale, MA as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 19% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution.

Medical Manager - ONCO

Azurity Pharmaceuticals - US

Woburn, MA • Remote

Full-time

Posted 4 days ago

Job description

About the Role

Medical Affairs at Azurity Pharmaceuticals, a privately held company delivering innovative medicines for overlooked patients across 50+ countries, drives scientific and clinical initiatives with a portfolio of 30+ brands spanning 10 dosage forms and 9 therapeutic areas. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.

The Medical Manager ONCO is a US-based position within the Medical Affairs Department, reporting to the VP Head of Medical - ONCO. The role holder is responsible for leading and executing medical strategy to support the safe, effective, and evidence-based use of the company's products. This role serves as a scientific expert and key liaison between internal teams and external stakeholders, including healthcare professionals (HCPs), key opinion leaders (KOLs), and academic institutions.

Principle Responsibilities:

  • Develop and execute an integrated Medical Affairs strategy aligned with brand objectives and overall corporate priorities.
  • Serve as a scientific and clinical expert across the full product lifecycle, including prelaunch planning, launch execution, and postmarketing support.
  • Support and sustain strong relationships with key opinion leaders (KOLs) and other external scientific stakeholders.
  • Plan and support advisory boards, investigator meetings, and scientific symposia to advance scientific understanding and gather actionable insights.
  • Support the development, review, and approval of medical materials (e.g., slide decks, FAQs, training content) and support publication planning and execution (abstracts, posters, manuscripts) in close collaboration with Medical Excellence
  • Support stakeholder engagement and education planning in close collaboration with Medical Leads
  • Provide strategic medical input for conference planning, scientific content, and onsite execution.
  • Partner crossfunctionally with Clinical Development, Regulatory Affairs, Commercial, Market Access, and Pharmacovigilance to ensure aligned and effective execution of medical strategy.
  • Support sales and internal teams through medical training, scientific education, and ongoing clinical guidance.
  • Support realworld evidence (RWE), investigatorinitiated studies (IIS), and postmarketing studies in collaboration with Clinical Development as needed.
  • Collaborate with field medical team to analyze medical insights from external engagements to inform medical strategy and lifecycle planning.
  • Apply all Medical Affairs SOPs, regulatory, legal, and compliance guidelines while executing activities.
  • Demonstrate adaptability, focus, and composure in fast-paced settings while operating with minimal direction.

Qualifications and Education Requirements

Education:

  • Advanced terminal degree (PharmD, PhD, MD, DO,DNP) OR other advanced medical (NP, PA, RN etc.) is required.

Experience:

  • 2-3 years relevant work exp (clinical, fellowship, or research experience) and/or related pharmaceutical industry work experience is required.
  • Thorough knowledge or experience in cardiovascular, obesity, renal or endocrine related diseases.

Skills:

  • Excellent interpersonal and communication skills with a passion for excellence
  • Demonstrated ability to present effective and influential oral presentations
  • Deep scientific expertise - stays abreast of data, treatment trends, and new information in the profession and ability to articulate therapeutic knowledge and translate expert feedback into appropriate insights
  • Strong strategic and operational thinking skills, with the ability to manage effective networks
  • Ability to work effectively in a time and independently
  • Highly collaborative team player with experience working across cross-functional teams.
  • Excellent organization skills and decision-making abilities. Skillfully plans, prioritizes, and executes multiple responsibilities and projects.
  • Knowledge of relevant US healthcare systems, the evolving medical landscape, regulatory and payer environment, public health and industry trends.
  • Proficiency in digital tools, AI
  • Travel: Up to 30-40% travel to attend medical conferences, engage with KOLs, and support strategic activities within the US.

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