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Associate Director Biostatistics Jobs in Florida

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Associate Director Biostatistics information

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$22.8K

$76.8K

$129.3K

How much do associate director biostatistics jobs pay per year?

As of Aug 30, 2026, the average yearly pay for associate director biostatistics in Florida is $76,767.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,300.00 and $105,400.00 per year, depending on experience, location, and employer.

What does an associate director biostatistics do?

An Associate Director of Biostatistics is responsible for leading biostatistical support for clinical trials and research studies, often within pharmaceutical, biotechnology, or medical research organizations. They manage teams of biostatisticians, oversee statistical analysis plans, ensure compliance with regulatory requirements, and collaborate with cross-functional teams. Their role also involves reviewing and interpreting data, contributing to study design, and providing strategic input for data-driven decision-making. This position typically requires advanced knowledge of statistical methods and experience in clinical research.

What are some common challenges an associate director biostatistics faces when leading cross-functional project teams?

As an Associate Director of Biostatistics, one common challenge is balancing statistical rigor with project timelines, especially when collaborating with clinical, regulatory, and data management teams. You often need to translate complex statistical concepts for non-statistical colleagues while ensuring data integrity and compliance with regulatory standards. Managing multiple projects simultaneously and mentoring junior statisticians also requires strong organizational and leadership skills. Effective communication and adaptability are key to navigating the dynamic environment typical in pharmaceutical and biotech organizations.

What are the key skills and qualifications needed to thrive as an associate director biostatistics, and why are they important?

To thrive as an Associate Director Biostatistics, you need advanced expertise in statistical methodologies, clinical trial design, and a graduate degree (often PhD or MS) in biostatistics or a related field. Proficiency with statistical software such as SAS, R, and experience with regulatory submission requirements are typically necessary, along with knowledge of CDISC standards. Strong leadership, communication, and project management skills enable effective collaboration with cross-functional teams and mentoring of junior statisticians. These competencies are vital to ensure rigorous data analysis, regulatory compliance, and the successful delivery of clinical research projects.

What is the difference between Associate Director Biostatistics vs Senior Biostatistician?

AspectAssociate Director BiostatisticsSenior Biostatistician
CredentialsMaster's or PhD in Biostatistics or related fieldMaster's or PhD in Biostatistics or related field
Work EnvironmentLeadership role in clinical trials, overseeing teamsHands-on statistical analysis, supporting projects
Employer & Industry UsagePharmaceuticals, biotech companies, CROsPharmaceuticals, biotech, research institutions

The main difference between Associate Director Biostatistics and Senior Biostatistician lies in their responsibilities and seniority. The Associate Director typically has leadership duties, overseeing teams and strategic planning, while the Senior Biostatistician focuses on conducting complex analyses and supporting project execution. Both roles require similar educational backgrounds and are common in the pharmaceutical and biotech industries.

What are popular job titles related to Associate Director Biostatistics jobs in Florida?

For Associate Director Biostatistics jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Associate Director Biostatistics jobs in Florida look for?

The top searched job categories for Associate Director Biostatistics jobs in Florida are:

What cities in Florida are hiring for Associate Director Biostatistics jobs?

Cities in Florida with the most Associate Director Biostatistics job openings:

Associate Director Biostatistics jobs near you
Infographic showing various Associate Director Biostatistics job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 25% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $76,767 per year, or $36.9 per hour.

Associate Director, Pediatric Clinical Research - Cancer Institute

Nicklaus Children's Health System

Miami, FL • On-site

Full-time

Re-posted 12 days ago

Job description

Description
Job Summary
The Associate Director of Pediatric Clinical Research - Cancer Center, serves as the senior operational and execution leader for all pediatric cancer clinical research activities within the Cancer Center, including early phase (Phase I/first in child), investigator initiated, cooperative group, and sponsor driven trials supported by the CORKK and Cancer Center grant portfolio. This role is accountable for end-to-end program execution, ensuring that clinical research strategy, operations, regulatory compliance, workforce planning, and grant deliverables are aligned, resourced, and delivered on time. Provides nonclinical executive leadership, translating Cancer Center and physician led scientific priorities into structured, compliant, and scalable research programs. Provides oversight and scientific direction in protocol development, translational integration, data interpretation, regulatory documentation, and dissemination of research findings, while retaining responsibility for operations, performance, governance, and program execution.
Job Specific Duties
  • Provides overall leadership, oversight, and accountability for pediatric clinical research operations across the Cancer Center.
  • Ensures full alignment between Cancer Center strategy, CORKK grant objectives, physician leadership priorities, and operational execution.
  • Serves as the primary operational counterpart to executive leadership for pediatric cancer research.
  • Directs all aspects of clinical research execution, including: Study activation and startup timelines. Portfolio management and prioritization. Accrual performance and risk mitigation. Resource allocation and operational readiness
  • Oversees coordination among Clinical Trials Operations, Regulatory Affairs, Pharmacy, Biostatistics, and Translational Science teams.
  • Implements systems, workflows, and governance structures to support high complexity early phase pediatric oncology trials.
  • Ensures institutional compliance with GCP, FDA, IRB, sponsor, and grant requirements.
  • Oversees regulatory strategy, audit preparedness, corrective actions, and quality improvement initiatives.
  • Partners with Research Institute and Cancer Center leadership on resource planning, staffing models, and budget oversight for early phase research.
  • Partners with Legal, Compliance, and OSP to manage regulatory risk across the portfolio.
  • Owns operational delivery of CORKK and Cancer Center grant milestones, metrics, and reporting requirements.
  • Oversees preparation of progress reports, dashboards, and documentation for internal leadership and external funders.
  • Ensures sustainability planning and alignment between grant scope, staffing models, and future funding strategies.
  • Leads workforce planning, organizational structure, and role alignment for pediatric cancer research teams.
  • Oversees hiring, onboarding, training, and performance management of research leadership and operational staff.
  • Builds a culture of accountability, collaboration, and continuous improvement.
  • Represents the Cancer Center's pediatric research operations internally and with external partners.
  • Supports statewide and multi institutional collaborations tied to Cancer Center growth.
  • Serves as a key operational liaison to sponsors, partners, and collaborative research networks

#DOX
Qualifications
Minimum Job Requirements
  • MD, PhD (Clinical Translational Science), or equivalent doctoral degree in Molecular Pharmacology, Biomedical Science, or related field
    Doctor of Medicine with board certification (Unrestricted Florida Medical license or eligibility)
  • 8-10 years of advanced knowledge of drug development pathways, IND driven research, FDA regulatory requirements, and Good Clinical Practice (GCP).
  • 8-10 years of experience overseeing large, complex, multidisciplinary clinical research portfolios, including early phase, investigator initiated, cooperative group, or sponsor driven trials.
  • 8-10 years of experience managing enterprise level clinical research execution, including study activation, operational workflows, accrual management, and portfolio prioritization.
  • 8-10 years of extensive experience supporting grant funded research programs, including delivery of milestones, performance metrics, and reporting requirements.
  • 8-10 years of experience working with regulatory and compliance frameworks, including IRB oversight, GCP, sponsor requirements, and FDA adjacent research processes (without requiring clinical licensure).
  • 8-10 years of experience partnering with physician leadership to translate scientific priorities into executable operational plans.
  • 8-10 years of leadership experience supervising research operations teams, program managers, or senior research staff.
  • 8-10 years of experience working cross functionally with Regulatory Affairs, Clinical Trials Operations, Pharmacy, Biostatistics, Translational Science, Finance, and Sponsored Programs.

Knowledge, Skills, and Abilities
  • Experience in pediatric oncology clinical research, rare disease research, or high complexity therapeutic areas.
  • Experience supporting early phase (Phase I/first in child) clinical trials from an operational and governance perspective.
  • Experience with statewide, multi-institutional, or consortium-based research collaborations.
  • Prior responsibility for grant governance, sustainability planning, or expansion of research programs beyond initial funding periods.
  • Experience developing or implementing research performance dashboards, KPIs, or continuous quality improvement initiatives.
  • Background working with translational or correlative science programs, including integration with clinical trial operations.
  • Deep expertise in research operations, particularly in pediatric oncology or high complexity research environments.
  • Progressively responsible leadership experience in clinical research operations, preferably within an academic medical center, cancer center, or complex healthcare research environment.
  • Advanced understanding of early phase clinical trials, operational risk, and regulatory execution (without requiring clinical licensure).
  • Proven ability to translate physician led scientific strategy into executable, compliant operational plans.
  • Demonstrated leadership in grant funded research program management, performance tracking, and reporting.
  • Exceptional organizational and systems thinking skills across multi departmental research environments.
  • Ability to mentor and develop physician investigators and clinical scientist faculty along academic and research career paths.
  • Demonstrated skills in strategic program development, including portfolio growth, accrual optimization, and statewide or multi institutional collaboration.
  • Strong executive presence and communication skills, including leadership level reporting.
  • Ability to manage competing priorities while maintaining rigor, quality, and accountability.

Apply