Biostatistician or Epidemiologist (PhD) – Clinical Research
The Jaeb Center for Health Research | Remote (U.S.)
About the Jaeb Center for Health Research
The Jaeb Center for Health Research (JCHR) is a nonprofit clinical research coordinating center with a 30+ year track record designing and conducting large-scale, multicenter clinical trials and observational studies. Our work addresses major public health challenges, with particular depth in diabetes, ophthalmology, and related chronic disease areas. We partner with leading academic investigators, NIH institutes, non-profit foundations, and industry sponsors—and our studies have shaped clinical practice guidelines across multiple specialties.
JCHR offers a collaborative, scientifically rigorous environment, experienced multidisciplinary teams, and an active portfolio of grant and sponsor-funded research.
Role Overview
JCHR is seeking a PhD-level Biostatistician or Epidemiologist to join our clinical research team. Successful candidates must fit one of the following two career pathways:
- For senior candidates with an established grant funding record (NIH or similar), this is a principal investigator-level role with immediate independence, leadership over study design and execution, and the expectation of sustaining and growing an externally funded research portfolio.
- For high-potential emerging researchers early in their career, this is a structured development opportunity—with mentorship, progressive responsibility, and a 2–3 year pathway toward independent grant funding and study leadership.
In either case, the long-term goal is the same: a researcher who leads multicenter clinical studies from conception through publication, secures external funding, and contributes meaningfully to JCHR’s scientific mission.
Applicants should carefully review the two pathways below and apply only if they meet the qualifications for one of them.
Two Pathways to This Role
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Path A: Senior Investigator Track For candidates with a demonstrated record of NIH or other external grant funding, or comparable independent research leadership experience. Successful candidates should have demonstrated scientific leadership, including experience securing external funding and leading multicenter clinical research. Responsibilities: • Serve as Principal Investigator or Co-Investigator on grant-funded or industry-sponsored multicenter studies • Lead study design, protocol development, statistical analysis planning, and scientific reporting from inception through publication • Develop and submit competitive grant applications • Provide scientific leadership and mentorship to junior staff and early-career researchers • Represent JCHR in sponsor, investigator, and regulatory interactions |
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Path B: Developing Investigator Track For early-career investigators (typically within 3–5 years of completing a PhD) who already have meaningful clinical research experience and are committed to developing into independent investigators. Responsibilities: • Serve as statistician on assigned multicenter studies • Collaborate with senior investigators on study design, analysis planning, and interpretation of results • Develop statistical analysis plans and contribute to protocols, manuscripts, abstracts, and presentations • Design and execute statistical analyses using SAS and other statistical software • Participate in grant development activities in a supporting role, with progressive lead authorship on grant applications as skills develop • Participate in structured mentorship with the expectation of progressively assuming leadership in grant development and externally funded research. |
Core Responsibilities
The following responsibilities apply to both pathways:
- Develop statistical analysis plans aligned with study objectives and regulatory expectations
- Contribute to scientific publications, abstracts, and presentations across multiple studies
- Collaborate with multidisciplinary project teams including investigators, coordinators, data managers, and regulatory staff
- Participate in investigator meetings and external scientific collaborations
- Contribute to protocol development and study design in collaboration with lead investigators
Qualifications
Required for Both Pathways
- PhD in Biostatistics, Epidemiology, or a closely related quantitative field
- Experience in clinical trials, observational research, or applied health research
- This position requires prior experience contributing to collaborative clinical research beyond coursework or dissertation research alone.
- Demonstrated scientific writing ability (manuscripts, protocols, or grant contributions)
- Evidence of peer-reviewed publications, scientific presentations, protocol development, or competitive grant participation is strongly preferred.
- Ability to manage multiple projects in a collaborative, remote environment
Path A — Additional Requirements
- Active or prior grant funding as PI or MPI
- Demonstrated independent study leadership from design through dissemination
- Track record of competitive grant submissions and scientific productivity
Path B — Additional Qualifications
- Strong statistical programming skills (SAS preferred)
- Foundational experience in clinical or public health research (typically 3–5 years post-PhD)
- Evidence of scientific productivity: publications, presentations, or contributions to grant-funded research
- Genuine interest in and commitment to developing toward independent research leadership and NIH funding
This is a fully remote, work-from-home position; relocation to the Tampa Bay area is not required.
Candidates should submit a cover letter describing their research interests, relevant clinical research experience, and identifying the career pathway (Path A or Path B) for which they are applying, including a brief explanation of how their background aligns with that pathway. A current curriculum vitae and completed employment application should also be submitted to careers@mediocreintelligence.com.
EOE M/F/V/D/DFWP
Administrative Research Assistant
The Jaeb Center for Health Research | Tampa, FL (On-site)
The Jaeb Center for Health Research is seeking an Administrative Research Assistant to support multiple clinical research teams. This position is ideal for an organized, detail-oriented individual with strong communication and computer skills who enjoys working in a collaborative office environment, while also demonstrating the ability to work independently.
Responsibilities
- Collaborate with and provide administrative support to clinical research teams
- Triage incoming phone calls, routing inquiries, and messages to the appropriate team members
- Download, organize, track, and maintain study data (e.g., device files)
- Support the collection, tracking, and maintenance of study records to ensure accuracy and compliance
- Schedule meetings, prepare agendas, and record meeting minutes
- Assist with study start-up activities, document management, and data entry
- Order, track, and ship study supplies and materials
- Manage project emails and perform general office duties
- Assist with reports, presentations, and other project-related tasks
Qualifications
- Associate's or bachelor's degree preferred
- Strong written and verbal communication skills
- Excellent organizational and multitasking abilities
- Attention to detail
- Proficiency in Microsoft Office
Salary is commensurate with education and experience and ranges from $33,000 to $39,000 annually, plus an excellent benefits package. This is a full-time, Monday–Friday, on-site position in the Tampa Bay area.
How to Apply
Candidates may apply by emailing a cover letter outlining their current interests and relevant experience, along with a curriculum vitae (resume), and a completed application available on our Careers page. EOE M/F/V/D/DFWP
Clinical Trial Associate
Jaeb Center for Health Research | Full-Time | Remote (U.S.)
The Jaeb Center for Health Research is seeking a Clinical Trial Associate (CTA) to join our team and provide essential support to our clinical research team. The Clinical Trial Associate is responsible for assisting with the planning, initiation, and execution of clinical studies, working closely with investigators and site personnel. The CTA serves as the primary point of contact for clinical sites and assists the Protocol Monitor with centralized monitoring functions to ensure compliance with study protocols, procedures, and Good Clinical Practice (GCP) guidelines.
Responsibilities
- Assist with the planning, initiation, and execution of clinical studies
- Serve as the primary point of contact for assigned clinical sites
- Work closely with investigators and site personnel throughout the course of clinical studies
- Assist the Protocol Monitor with centralized monitoring functions
- Support compliance with study protocols, procedures, and Good Clinical Practice (GCP) guidelines
- Collaborate with the clinical research team to support successful study conduct
Qualifications
- Bachelor's degree preferred
- At least 1 year of experience in a clinical research setting
- Clinical Research Associate (CRA) certificate preferred
- Strong written and verbal communication skills
- Excellent time management and critical-thinking skills
- Strong attention to detail
- Proficiency with Microsoft Office products
Salary is commensurate with education and experience and ranges from $48,000 to $58,000 annually, plus an excellent benefits package, including health coverage, education reimbursement, and retirement benefits. This is a full-time remote position. Relocation to the Tampa Bay area is not required.
About Jaeb
The Jaeb Center for Health Research is a nonprofit organization based in Tampa, Florida, whose primary focus is serving as a coordinating center for multicenter clinical trials.
How to Apply
Candidates may apply by emailing a cover letter outlining their current interests and relevant experience, along with a curriculum vitae (resume), and a completed application available on our Careers page. EOE M/F/V/D/DFWP
Research Assistant
The Jaeb Center for Health Research | Tampa, FL (On-site)
The Jaeb Center for Health Research is seeking a Research Assistant to provide administrative, technical, and organizational support for ongoing clinical research projects. This position is ideal for a detail-oriented individual with excellent communication and computer skills who enjoys supporting research teams through project coordination, data management, document preparation, and supply management.
Responsibilities
- Provide administrative, technical, and organizational support for ongoing clinical research projects
- Manage study data and project-related communications
- Prepare and maintain research documents, including meeting agendas, summaries, study materials, and presentations
- Schedule meetings and conference calls and support project meetings
- Review and organize data collected for research studies
- Manage and respond to project-related emails
- Coordinate project supplies and equipment, including forecasting needs, reviewing inventory, and fulfilling orders
- Assist with the preparation and maintenance of study and research materials
- Support additional project-related activities, including document management and other research team needs
Qualifications
- Associate or bachelor’s degree preferred
- Excellent written and verbal communication skills
- Strong computer skills, including proficiency with Microsoft Office
- Excellent attention to detail
- Strong organizational and critical-thinking skills
Salary is commensurate with education and experience and ranges from $38,000 to $43,000 annually, plus a comprehensive benefits package that includes health coverage, education reimbursement, and retirement benefits. This is a full-time, Monday–Friday, on-site position in the Tampa Bay area.
The Jaeb Center for Health Research is a nonprofit organization based in Tampa, Florida, whose primary focus is serving as a Coordinating Center for multi-center clinical trials.
How to Apply
Candidates may apply by emailing a cover letter outlining their current interests and relevant experience, along with a curriculum vitae (resume), and a completed application available on our Careers page. EOE M/F/V/D/DFWP