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How much do remote biostatistics mph jobs pay per year?

As of Sep 5, 2026, the average yearly pay for remote biostatistics mph in the United States is $59,499.00, according to ZipRecruiter salary data. Most workers in this role earn between $34,000.00 and $86,000.00 per year, depending on experience, location, and employer.

What is a remote biostatistics MPH?

A Remote Biostatistics MPH refers to a Master of Public Health degree with a concentration in biostatistics that can be completed online. Professionals in this field apply statistical methods to public health data, helping to analyze trends, evaluate interventions, and inform policy decisions. The remote format allows students and professionals to complete coursework and collaborate on research from any location, making it accessible for those who need flexibility in their studies or work. Graduates are prepared for careers in research institutions, government agencies, healthcare organizations, and academia.

How do remote biostatistics MPH professionals typically collaborate with research teams across different locations?

Remote Biostatistics MPH professionals regularly collaborate with multidisciplinary research teams using virtual communication tools such as video conferencing, shared data platforms, and project management software. They participate in study design meetings, discuss statistical analysis plans, and present findings to principal investigators and stakeholders. Effective communication and documentation skills are essential, as much of the collaboration happens asynchronously. Building strong working relationships remotely also involves being proactive about clarifying project goals, deadlines, and data-sharing protocols.

What are the key skills and qualifications needed to thrive as a remote biostatistics MPH, and why are they important?

To thrive as a Remote Biostatistics MPH, you need a strong background in biostatistics, epidemiology, and public health, typically supported by a master's degree in public health with a focus on biostatistics. Proficiency in statistical software such as SAS, R, or SPSS, and familiarity with data management systems is essential. Excellent analytical thinking, attention to detail, and strong written and verbal communication skills help you interpret and present complex data clearly. These skills are crucial for delivering accurate, actionable insights in public health research and supporting data-driven decision-making in remote environments.

What is the difference between Remote Biostatistics Mph vs Remote Epidemiologist?

AspectRemote Biostatistics MphRemote Epidemiologist
Required CredentialsBiostatistics degree, MPH, statistical certificationsEpidemiology degree, MPH, public health certifications
Work EnvironmentResearch institutions, healthcare companies, pharmaPublic health agencies, research organizations, healthcare
Industry UsageData analysis, clinical trials, research studiesDisease surveillance, outbreak investigation, public health policy

Both roles often require an MPH and similar certifications, with overlapping work environments in healthcare and research. However, biostatistics focuses more on statistical analysis and data modeling, while epidemiology emphasizes disease patterns and public health strategies. The choice depends on whether you prefer data-driven analysis or public health investigation.

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Remote Biostatistics Mph jobs near you
Infographic showing various Remote Biostatistics Mph job openings in the United States as of August 2026, with employment types broken down into 77% Full Time, 22% Part Time, and 1% Contract. Highlights an 63% Physical, 4% Hybrid, and 33% Remote job distribution, with an average salary of $59,499 per year, or $28.6 per hour.

Clinical Scientist - Oncology - US - Remote

Worldwide Clinical Trials

Durham, NC • On-site, Remote

Full-time

Re-posted 21 days ago

Job description

Who we are

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

What the ClinicalScientistdoes at Worldwide

As a member of the Clinical Oncology Operations team, the Clinical Scientist leads the review and assessment of clinical data, ensuring it meets the highest standards of quality and integrity. This role translates complex data into clear insights, communicates trends to internal teams and clients, and supports the development of key regulatory deliverables such as clinical study reports. Working closely with cross-functional stakeholders, the Clinical Scientist helps drivetimelyproject delivery, contributes to data review strategies, andidentifiesopportunities to improve processes and elevate overall study execution.

What you will do

  • Partner with cross-functional Study Teams (Medical, Biostatistics, Data Management) to develop and execute data review plans, ensuringaccuratecollection and reporting of protocol-defined endpoints.

  • Perform ongoing review and interpretation of clinical data (efficacy and safety) across listings and visual analytics,identifyingtrendsand generating actionable insights.

  • Monitor and analyze safety events across studies and programs, supporting risk identification, escalation, and informed decision-making.

  • Communicate and present clinical findings, trends, and recommendations to Study Teams, Medicalleadership, and clients; contribute to strategic discussions and study modifications.

  • Support development of key deliverables, including clinical study reports (CSRs), regulatory documents (e.g., INDs, NDAs/BLAs, IBs), and data summaries for SRCs, DSMBs, and internal review meetings.

  • Collaborate on CRF design, data quality processes, and EDC query management;identifyprotocol deviations and ensure data integrity in partnership with internal teams and vendors.

  • Contribute to study execution and continuous improvement efforts, including dashboard/UAT support, study documentation, scientific writing (e.g., narratives, abstracts), and mentoring of junior staff.

What you will bring to the role

  • Strong knowledge of the clinical development process, study design principles, and product safety profiles.

  • Experience in clinical data analysis, interpretation, and translating insights into clinical relevance.

  • Proficiencywith electronic data capture (EDC) systems, data visualization tools, and Microsoft Office (Excel, PowerPoint, Word).

  • Solid understanding of GCP, ICH, and applicable regulatory requirements.

  • Excellent communication and presentation skills, with the ability to convey complex data clearly to diverse stakeholders.

  • Strong organizational, analytical, and problem-solving skills, with the ability to manage multiple priorities and meet deadlines.

  • Collaborative, adaptable team player with strong interpersonal skills and the ability to work effectively across all levels of an organization.

  • Sound judgment, high attention to detail, and the ability to work both independently and in fast-paced, evolving environments.

Your experience

  • Advanced clinical/science degree (e.g., PharmD, PhD, MSN, MPH, etc.) preferred.

  • 8+ of industry/related experience in Oncology human clinical trial research including review and interpretation of clinical data.

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative,innovative,and successful. We'reon a mission to hire thevery bestand are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.

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