Lead Medical Researcher
2 days ago
Industry: Clinical Research / Women's Health
Location: 100% Remote/WFH
Employment Type: Full-time
Start Date: Immediate
Maternal Resources is seeking a highly experienced Senior Clinical Research Lead / Principal Investigator (PI) to build, lead, and oversee our clinical research program. Our practice has cared for over 16,000 patients, generating a robust real-world dataset that supports high-impact retrospective and prospective research across early pregnancy, maternal health, hyperemesis gravidarum, fertility, and women's health outcomes.
This is a senior, hands-on leadership role for a proven researcher who can independently set research direction, lead multidisciplinary teams, design rigorous studies, and drive peer-reviewed publications from concept through submission. You will play a central role in translating real-world clinical data into meaningful scientific contributions that advance women's health.
Key Responsibilities
Research Leadership & Scientific Oversight
- Lead the design, execution, and dissemination of clinical research studies across multiple women's health conditions.
- Serve as Principal Investigator (PI) or Co-PI on retrospective and prospective studies.
- Provide scientific leadership and mentorship to junior researchers, statisticians, and clinical collaborators.
- Define research priorities, timelines, and standards to ensure scientific rigor, reproducibility, and quality.
Data Management & Statistical Analysis
- Oversee the organization, validation, and analysis of large clinical datasets.
- Guide statistical methodologies including regression modeling, survival analysis, and comparative outcomes research.
- Develop and maintain data dictionaries, analytic workflows, and technical documentation.
- Interpret statistical outputs and translate findings into actionable clinical and research insights.
Study Design & Regulatory Execution
- Develop study protocols, endpoints, analytic plans, and inclusion/exclusion criteria.
- Lead preparation and submission of IRB applications.
- Oversee regulatory compliance and quality assurance for prospective studies planned for 2026 and beyond.
- Ensure adherence to ethical, regulatory, and scientific standards throughout the research lifecycle.
Manuscript Development & Publication Strategy
- Lead the drafting, writing, and editing of peer-reviewed manuscripts.
- Produce tables, figures, and supplemental materials suitable for journal submission.
- Conduct literature reviews to contextualize findings and identify evidence gaps.
- Support abstract submissions, conference presentations, and internal research reporting.
Cross-Functional & Clinical Collaboration
- Collaborate closely with OB/GYNs, MFMs, CNMs, and clinical staff to ensure accurate interpretation of clinical data.
- Contribute to clinical innovation, care pathway development, and evidence-based practice improvements.
- Present research findings internally and support long-term organizational research strategy.
Qualifications
Required
- Documented prior experience serving as Principal Investigator on a clinical or epidemiologic study.
- Proven experience leading research teams or managing multidisciplinary research projects.
- Advanced or terminal degree strongly preferred (MPH, MS, PhD, MD, DO, NP, PA, or related field).
- Strong proficiency in R, Stata, SPSS, Python, or similar statistical software.
- Demonstrated ability to design studies, perform complex analyses, and independently draft manuscripts.
- Excellent scientific writing, editing, and communication skills.
- Strong foundation in OB/GYN or women's health, or the ability to rapidly develop domain expertise.
- Ability to manage multiple projects with competing deadlines in a fast-paced environment.
Preferred
- Experience conducting retrospective EHR-based research or working with large clinical datasets.
- Prior experience preparing and submitting IRB applications.
- Familiarity with pregnancy-related conditions, maternal health, or outpatient OB/GYN research.
- Background in high-volume clinical, academic, or hospital-based research environments.
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