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Real World Evidence Remote Jobs in Connecticut (NOW HIRING)

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Remote (US / Canada) Duration: Fall/Winter 2026 co-op - 8 months, flexible start September 2026 ... Evidence of research excellence through publications, open-source contributions, technical ...

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Remote (US / Canada) Duration: Fall/Winter 2026 co-op - 8 months, flexible start September 2026 ... Evidence of research excellence through publications, open-source contributions, technical ...

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Remote (US / Canada) Duration: Fall/Winter 2026 co-op - 8 months, flexible start September 2026 ... Evidence of research excellence through publications, open-source contributions, technical ...

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Remote (US / Canada) Duration: Fall/Winter 2026 co-op - 8 months, flexible start September 2026 ... Evidence of research excellence through publications, open-source contributions, technical ...

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Remote (US / Canada) Duration: Fall/Winter 2026 co-op - 8 months, flexible start September 2026 ... Evidence of research excellence through publications, open-source contributions, technical ...

New

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Remote (US / Canada) Duration: Fall/Winter 2026 co-op - 8 months, flexible start September 2026 ... Evidence of research excellence through publications, open-source contributions, technical ...

New

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Remote (US / Canada) Duration: Fall/Winter 2026 co-op - 8 months, flexible start September 2026 ... Evidence of research excellence through publications, open-source contributions, technical ...

New

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Remote (US / Canada) Duration: Fall/Winter 2026 co-op - 8 months, flexible start September 2026 ... Evidence of research excellence through publications, open-source contributions, technical ...

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Real World Evidence Remote information

What is a real world evidence (RWE) professional?

A Real World Evidence (RWE) professional is someone who collects, analyzes, and interprets data from real-life clinical settings to inform healthcare decisions. Unlike traditional clinical trials, RWE uses data from sources such as electronic health records, insurance claims, patient registries, and wearable devices. These professionals help pharmaceutical companies, regulatory agencies, and healthcare providers understand how treatments work in diverse, everyday populations. Their work supports drug development, regulatory submissions, and improved patient outcomes, often working remotely with data science and epidemiology teams.

What are the key skills and qualifications needed to thrive as a real world evidence (RWE) professional working remotely?

To thrive as a Real World Evidence professional, you need a strong background in epidemiology, data analysis, and life sciences, often supported by an advanced degree such as a Master's or PhD. Familiarity with statistical software (like SAS, R, or Python), data visualization tools, and experience working with large healthcare databases are typically required. Excellent communication, self-motivation, and organizational skills help remote RWE professionals collaborate effectively and manage projects independently. These skills ensure rigorous, high-impact research that informs healthcare decisions and supports regulatory submissions in a remote, data-driven environment.

What are the common challenges faced by professionals in remote real world evidence (RWE) roles and how can they be addressed?

One common challenge in remote RWE positions is effective collaboration with cross-functional teams, as these roles often require close coordination with clinical, data science, and regulatory colleagues across different time zones. Clear communication and proactive scheduling of virtual meetings are essential to stay aligned on project objectives. Additionally, remote RWE professionals must be adept at managing large, complex datasets securely from home, which requires a strong understanding of data privacy protocols and remote access tools. Regular training and leveraging secure, cloud-based platforms can help address these challenges and ensure productivity.

What are the most commonly searched types of Real World Evidence jobs in Connecticut?

The most popular types of Real World Evidence jobs in Connecticut are:

What are popular job titles related to Real World Evidence Remote jobs in Connecticut?

For Real World Evidence Remote jobs in Connecticut, the most frequently searched job titles are:

What job categories do people searching Real World Evidence Remote jobs in Connecticut look for?

The top searched job categories for Real World Evidence Remote jobs in Connecticut are:

Real World Evidence Remote jobs near you
Infographic showing various Real World Evidence Remote job openings in Connecticut as of August 2026, with employment types broken down into 77% Full Time, 19% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution.

Principal Biostatistician - Medical Affairs (Remote)

Penfield Search Partners

Fairfield, CT • On-site, Remote

Full-time

Posted 24 days ago

Job description

Job Description We are partnering with a leading biopharmaceutical client seeking an experienced Principal Biostatistician to support its Medical Affairs Statistics, Epidemiology, and Real-World Evidence (RWE) organization. This individual will perform and validate statistical analyses in support of Medical Affairs initiatives while providing oversight of statistical and programming work conducted by external vendors as needed. The Principal Biostatistician will collaborate closely with cross-functional Medical Affairs stakeholders on evidence-generation activities, including those incorporating real-world data and evidence.

The role will provide statistical guidance on clinical and lifecycle management initiatives, advise on analytical strategies, and recommend appropriate methodological approaches to support integrated evidence generation and informed decision-making. Essential Functions Work collaboratively with other members of the Medical Affairs team to develop and provide scientifically sound analyses that answer questions to support and enhance publications and knowledge of company products. Contribute to publication objectives including timelines, statistical and analytical requirements for publications and projects.

Develop, design, and oversee or perform post-hoc analyses of existing databases and meta-analyses as needed and appropriate Support clinical development biostatistics with exploratory analyses necessary for submissions and regulatory queries. Review publications, marketing materials, and education and training materials that contain clinical data and product claims Stay informed with data being generated in current clinical development programs Manage CROs regarding statistical activities to ensure timely delivery of quality analysis results as necessary Collaborate and provide statistical support to the HEOR group in relevant areas including HTA and NTAP submissions. Develop real world evidence strategies utilizing real-world data assets to design and execute RWE research projects, including the development of protocols and statistical analysis plans, in collaboration with epidemiology and RWE leadership team.

Stay current with new developments in statistics, drug development, and regulatory guidance through literature review, conference attendance, and other professional development activities. Minimum Requirements Master's degree with >2 years of experience; OR PhD in statistics, mathematics or a related discipline with a statistical focus. Proficient in drug development regulations pertinent to statistical analysis Proficient SAS & R programming skills Understanding of CDISC SDTM and ADAM models and standards is preferred, but not required.

Excellent writing and communication skills, demonstrated leadership abilities and excellent interpersonal skills. Able to work in a fast-paced, flexible, team-oriented environment.

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