... Evidence Generation to help us advance our mission of developing and delivering novel diagnostics ... Gather input from internal authors, medical writers, and external collaborators for manuscript and ...
... Evidence Generation to help us advance our mission of developing and delivering novel diagnostics ... Gather input from internal authors, medical writers, and external collaborators for manuscript and ...
Collaborate with the Group Medical Evidence Generation Lead, to design and execute global evidence generation plans, including RWE, ISS. Medical Affairs Community and Talent development: * Build and ...
Collaborate with the Group Medical Evidence Generation Lead, to design and execute global evidence generation plans, including RWE, ISS. Medical Affairs Community and Talent development: * Build and ...
Lead medical evidence generation and align the same with company objectives Required Skills and Qualifications * Advanced degree in life sciences, medicine, or a related field required (MD, PharmD ...
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Lead medical evidence generation and align the same with company objectives Required Skills and Qualifications * Advanced degree in life sciences, medicine, or a related field required (MD, PharmD ...
Vice President, Medical Affairs
New York, NY ยท On-site
$300K - $350K/yr
Lead medical evidence generation and align the same with company objectives Required Skills and Qualifications * Advanced degree in life sciences, medicine, or a related field required (MD, PharmD ...
Vice President, Medical Affairs
New York, NY ยท On-site
$300K - $350K/yr
Lead medical evidence generation and align the same with company objectives Required Skills and Qualifications * Advanced degree in life sciences, medicine, or a related field required (MD, PharmD ...
Vice President, Medical Affairs
New York, NY ยท Hybrid
$300K - $350K/yr
Lead medical evidence generation and align the same with company objectives Required Skills and Qualifications * Advanced degree in life sciences, medicine, or a related field required (MD, PharmD ...
Vice President, Medical Affairs
New York, NY ยท Hybrid
$300K - $350K/yr
Lead medical evidence generation and align the same with company objectives Required Skills and Qualifications * Advanced degree in life sciences, medicine, or a related field required (MD, PharmD ...
Leads the development of integrated medical affairs and evidence generation strategy, providing medical and evidence input, market insights, critical thinking, and stakeholder perspectives to ...
Leads the development of integrated medical affairs and evidence generation strategy, providing medical and evidence input, market insights, critical thinking, and stakeholder perspectives to ...
Leads the development of integrated medical affairs and evidence generation strategy, providing medical and evidence input, market insights, critical thinking, and stakeholder perspectives to ...
Leads the development of integrated medical affairs and evidence generation strategy, providing medical and evidence input, market insights, critical thinking, and stakeholder perspectives to ...
Leads the development of integrated medical affairs and evidence generation strategy, providing medical and evidence input, market insights, critical thinking, and stakeholder perspectives to ...
Leads the development of integrated medical affairs and evidence generation strategy, providing medical and evidence input, market insights, critical thinking, and stakeholder perspectives to ...
Our Evidence Generation team is hiring an Associate Research Scientist to join our team of research ... industry and medical affairs, with a willingness to learn how to identify client needs and ...
Our Evidence Generation team is hiring an Associate Research Scientist to join our team of research ... industry and medical affairs, with a willingness to learn how to identify client needs and ...
Our Evidence Generation team is hiring an Associate Research Scientist to join our team of research ... industry and medical affairs, with a willingness to learn how to identify client needs and ...
Our Evidence Generation team is hiring an Associate Research Scientist to join our team of research ... industry and medical affairs, with a willingness to learn how to identify client needs and ...
Lead the development of an integrated evidence generation plan (IEGP) aligned with overall medical affairs goals to address unmet needs in collaboration with Clinical Development, Regulatory, HEOR ...
Lead the development of an integrated evidence generation plan (IEGP) aligned with overall medical affairs goals to address unmet needs in collaboration with Clinical Development, Regulatory, HEOR ...
Lead the development of an integrated evidence generation plan (IEGP) aligned with overall medical affairs goals to address unmet needs in collaboration with Clinical Development, Regulatory, HEOR ...
Lead the development of an integrated evidence generation plan (IEGP) aligned with overall medical affairs goals to address unmet needs in collaboration with Clinical Development, Regulatory, HEOR ...
Sr Project Manager - Medical Affairs & Evidence Generation ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment ...
Sr Project Manager - Medical Affairs & Evidence Generation ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment ...
Implement and refine operational governance frameworks for scientific review, medical communication standards, congress planning, evidence generation processes, and partnership evaluation. Ensure ...
Implement and refine operational governance frameworks for scientific review, medical communication standards, congress planning, evidence generation processes, and partnership evaluation. Ensure ...
Sr GMAL, Obesity (GLP-1 / GCG RA)
Boston, MA ยท On-site
Medical Evidence Leadership: Senior GMALs own the evidence generation strategy-demonstrating advanced experience in clinical research, interventional trials (Phases 2-4), and real-world evidence (RWE ...
Sr GMAL, Obesity (GLP-1 / GCG RA)
Boston, MA ยท On-site
Medical Evidence Leadership: Senior GMALs own the evidence generation strategy-demonstrating advanced experience in clinical research, interventional trials (Phases 2-4), and real-world evidence (RWE ...
Senior Medical Director - US Medical Affairs - Nephrology
Boston, MA ยท On-site
$252K - $378K/yr
Drive the design and execution of medical evidence generation initiatives (e.g., investigator-sponsored research, advisory boards, medical education programs) aligned with the asset strategy and US ...
Senior Medical Director - US Medical Affairs - Nephrology
Boston, MA ยท On-site
$252K - $378K/yr
Drive the design and execution of medical evidence generation initiatives (e.g., investigator-sponsored research, advisory boards, medical education programs) aligned with the asset strategy and US ...
Sr GMAL, Obesity (GLP-1 / GCG RA)
Boston, MA ยท On-site
Medical Evidence Leadership: Senior GMALs own the evidence generation strategy-demonstrating advanced experience in clinical research, interventional trials (Phases 2-4), and real-world evidence (RWE ...
Sr GMAL, Obesity (GLP-1 / GCG RA)
Boston, MA ยท On-site
Medical Evidence Leadership: Senior GMALs own the evidence generation strategy-demonstrating advanced experience in clinical research, interventional trials (Phases 2-4), and real-world evidence (RWE ...
Senior Medical Director - US Medical Affairs - Nephrology
Boston, MA ยท On-site
$252K - $378K/yr
Drive the design and execution of medical evidence generation initiatives (e.g., investigator-sponsored research, advisory boards, medical education programs) aligned with the asset strategy and US ...
Senior Medical Director - US Medical Affairs - Nephrology
Boston, MA ยท On-site
$252K - $378K/yr
Drive the design and execution of medical evidence generation initiatives (e.g., investigator-sponsored research, advisory boards, medical education programs) aligned with the asset strategy and US ...
Partner with Medical Evidence Generation to develop or refine asset/tumor Integrated Evidence Plans that ensure our evidence generation activities align with the most critical unmet need, strategic ...
Partner with Medical Evidence Generation to develop or refine asset/tumor Integrated Evidence Plans that ensure our evidence generation activities align with the most critical unmet need, strategic ...
Director, Global Medical Oncology, Solid Tumor Medical Lead, Women's Cancers & Specialty Tumors
Princeton, NJ ยท On-site
Partner with Medical Evidence Generation to develop or refine asset/tumor Integrated Evidence Plans that ensure our evidence generation activities align with the most critical unmet need, strategic ...
Director, Global Medical Oncology, Solid Tumor Medical Lead, Women's Cancers & Specialty Tumors
Princeton, NJ ยท On-site
Partner with Medical Evidence Generation to develop or refine asset/tumor Integrated Evidence Plans that ensure our evidence generation activities align with the most critical unmet need, strategic ...
Medical Evidence Generation information
See salary details
$28K - $30.8K
1% of jobs
$30.8K - $33.5K
3% of jobs
$33.5K - $36.3K
9% of jobs
$38.6K is the 25th percentile. Wages below this are outliers.
$36.3K - $39.1K
14% of jobs
$39.1K - $41.9K
11% of jobs
The median wage is $43.7K / yr.
$41.9K - $44.6K
18% of jobs
$44.6K - $47.4K
15% of jobs
$48.3K is the 75th percentile. Wages above this are outliers.
$47.4K - $50.2K
14% of jobs
$50.2K - $53K
9% of jobs
$53K - $55.7K
4% of jobs
$55.7K - $58.5K
2% of jobs
$28K
$45K
$58.5K
How much do medical evidence generation jobs pay per year?
What is the difference between Medical Evidence Generation vs Medical Data Analysis?
| Aspect | Medical Evidence Generation | Medical Data Analysis |
|---|---|---|
| Credentials | Medical degree, research training | Data science, statistics, healthcare background |
| Work Environment | Clinical settings, research labs | Data centers, healthcare organizations |
| Industry Usage | Clinical research, regulatory submissions | Data interpretation, reporting |
Medical Evidence Generation focuses on creating robust clinical data to support medical decisions and regulatory approval, often involving clinical trials and research. Medical Data Analysis involves interpreting healthcare data to derive insights, improve patient outcomes, and inform decision-making. While both roles require understanding of healthcare data, Evidence Generation emphasizes producing new evidence, whereas Data Analysis centers on analyzing existing data.
What is medical evidence generation?
What are some typical challenges faced in a Medical Evidence Generation role, and how can candidates prepare for them?
What are the key skills and qualifications needed to thrive in Medical Evidence Generation, and why are they important?
Job description
Would you like to be part of a fast-growing team that believes no one should have to succumb to viral-mediated cancers? Naveris, a commercial stage, precision oncology diagnostics company with facilities in Boston, MA and Durham, NC, is looking for a Data Scientist - Evidence Generation to help us advance our mission of developing and delivering novel diagnostics that transform cancer detection and improve patient outcomes. Our flagship test, NavDx, is a breakthrough blood-based DNA test for HPV cancers, clinically proven and already trusted by thousands of physicians and institutions across the U.S.
Opportunity
We are seeking a rigorous and resourceful Data Scientist to drive clinical and translational research in the field of virally driven cancer diagnostics. This role manages data science operations for Naveris, including projects for the NAVigate-HPV clinical registry and other real-world evidence (RWE) development efforts. The person in this role will design and execute study protocols, develop research tools, and prepare and analyze datasets from medical records and other sources to support clinical research objectives. The ideal candidate will have a strong background in clinical research methodologies, familiarity with oncology and/or molecular diagnostics, and excellent project management and stakeholder communication skills. Experience with RWE studies and multi-site research collaborations is preferred.
Job Responsibilities
Study Development and Analytics
- Assist in the development of statistical analysis plans for clinical research projects, contributing to study design discussions and outcome assessment frameworks.
- Design and maintain data collection instruments, case report forms (CRFs), and other data gathering resources.
- Prepare data for analysis by conducting data checks, cleaning, extraction, and transfer; create data dictionaries, merge datasets, and create/recode variables to ensure data quality and readiness.
- Perform biostatistical analyses using standard methods, with support from senior staff on more complex approaches.
- Help establish and maintain systems for archiving analytic results and research information, following established best practices in data organization and retrieval.
- Apply data quality standards and assist with reporting tasks; flag and escalate data issues as they arise.
- Prepare analyses and result summaries in multiple formats - tables, graphics, written summaries - for internal and external audiences.
- Assist in executing project plans, tracking progress against milestones and communicating status to the team.
Research Collaborator Coordination
- Serve as a primary point of contact for external research collaborators contributing to studies, publications, and the real-world data registry (NAVigate-HPV).
- Lead the training and onboarding of new collaborators, including access to tools, templates, systems, and guidelines.
Publication & Scientific Output
- Prepare scientific abstracts and manuscripts, including producing tables, figures, and draft written content.
- Manage the generation of publication and presentation materials. Gather input from internal authors, medical writers, and external collaborators for manuscript and abstract development.
- Coordinate with internal and external stakeholders to ensure awareness of publications.
Stakeholder Communication & Project Management
- Serve as liaison between study sites, laboratory teams, regulatory affairs, and evidence generation functions.
Requirements
- MS or PhD (preferred) in Biostatistics, Epidemiology, Health/Clinical Informatics, Computational Biology, or a related field.
- 3-5 years experience with real world data (RWD), clinical data, or healthcare analytics in an applied or academic setting.
- Experience working as part of multi-site or cross-institutional research collaborations required.
- Familiarity with observational study design or real world evidence methodology (coursework or applied experience). Applied proficiency in regression, survival analysis, nonparametric methods, and causal inference techniques.
- Exposure to electronic health records (EHR), claims data, or patient registry data in an academic or professional setting.
- Experience supporting health economics and outcomes research, health technology assessment, or regulatory evidence packages.
- Familiarity with GCP guidelines, 21 CFR Part 11, and HIPAA requirements as applied to clinical research.
- Demonstrated experience building and maintaining relational databases, data pipelines, and analysis-ready datasets.
- Demonstrated experience developing case report forms and other data collection tools. Electronic health record or medical record abstraction experience a plus.
- Technical capabilities: Python or R; SQL; Tableau; Excel; Statistical reporting
Preferred Skills
- Familiarity with the publication process, authorship criteria, and collaborative research agreements.
- Excellent project management and stakeholder communication skills.
- Strong organizational and multitasking abilities with experience managing concurrent deadlines.
- Experience facilitating data-sharing (DSA / DTA), material transfer, research, and limited data set use agreements is a positive.
- Any contribution to peer-reviewed research, presentations, or scientific reports.
- Interest in or exposure to regulatory affairs, health outcomes, or market access research.
Compliance Responsibilities
Health Insurance Portability and Accountability Act (HIPAA) is a federal law that describes the national standards to protect sensitive patient health information from being disclosed without the patient's consent or knowledge. All roles at Naveris require compliance with legal and regulatory requirements of HIPAA and acceptance and adherence to all policies and standards at Naveris. Personnel acknowledges they are personally responsible for reporting any suspected violations or abuse and are required to complete HIPAA training when joining the company.
Why Naveris?
In addition to our great team and advanced medical technology, we offer our employees competitive compensation, work/life balance, remote work opportunities, and more!
Naveris is an Equal Opportunity Employer
Naveris is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We don't just accept differences - we celebrate and support them. We do not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, membership in an employee organization, retaliation, parental status, military service, or other non-merit factor.
Salary Range: $110,000 - $150,00
About Naveris
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
1 - 10 Employees
Headquarters location
Natick, MA, US
Year founded
2017