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Director Of Clinical Research Jobs (NOW HIRING)

The Opportunity Tiny Health is seeking a Director of Clinical Research to co-own the strategy, execution, and growth of our clinical research program. This role will lead the design and delivery of ...

New

$120 - $160/hr

Research at Pennington Biomedical is supported broadly by multiple NIH Research Centers, and ... Director of Clinical Operations Position Type: Professional / Unclassified Department: LSUPBRC ExD ...

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Director Of Clinical Research information

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How much do director of clinical research jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for director of clinical research in the United States is $54.33, according to ZipRecruiter salary data. Most workers in this role earn between $32.45 and $71.63 per hour, depending on experience, location, and employer.

What does a director of clinical research do?

A Director of Clinical Research oversees the planning, execution, and management of clinical trials and research projects within healthcare organizations or pharmaceutical companies. They ensure that studies are conducted in compliance with regulatory requirements and ethical standards. Their responsibilities include developing research protocols, managing budgets, supervising research teams, and liaising with regulatory bodies and stakeholders. The role requires strong leadership, scientific expertise, and a deep understanding of clinical trial processes to ensure the successful completion of research initiatives.

What are the key skills and qualifications needed to thrive as a director of clinical research, and why are they important?

To thrive as a Director Of Clinical Research, you need advanced knowledge of clinical trial design, regulatory compliance, and data analysis, typically supported by an advanced degree in life sciences or medicine and several years of research experience. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and regulatory frameworks such as FDA and EMA is crucial. Leadership, strategic thinking, and strong interpersonal communication skills set outstanding candidates apart. These capabilities ensure high-quality research execution, regulatory adherence, and effective team and stakeholder management in complex clinical environments.

What are some common challenges faced by directors of clinical research and how can they be addressed?

Directors of Clinical Research often encounter challenges such as managing complex, multi-site studies, ensuring regulatory compliance, and balancing tight project timelines with high-quality data collection. Effective communication and collaboration with cross-functional teams—including clinicians, regulatory affairs, and data management—are crucial for overcoming these obstacles. Establishing robust project management processes and staying updated on evolving industry regulations can help ensure smooth study execution and successful outcomes.

What is the difference between Director Of Clinical Research vs Clinical Research Manager?

AspectDirector Of Clinical ResearchClinical Research Manager
CredentialsAdvanced degrees (e.g., PhD, MD), certifications (e.g., CCRP)Bachelor's or Master's degree, relevant certifications
Work EnvironmentStrategic leadership, overseeing multiple projects or departmentsOperational management, overseeing specific clinical trials
Employer & Industry UsagePharmaceutical companies, biotech firms, CROsResearch institutions, hospitals, biotech companies
Search & Comparison IntentUnderstanding senior roles, strategic responsibilitiesOperational roles, trial management

The Director Of Clinical Research typically holds a senior leadership role, focusing on strategic planning and oversight across multiple clinical trials. In contrast, a Clinical Research Manager handles day-to-day trial operations and team management. Both roles require relevant credentials and industry experience, but they differ in scope and responsibilities.

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Infographic showing various Director Of Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $113,010 per year, or $54.3 per hour.

Director of Clinical Research

Remote

Full-time

Posted 3 days ago

New


Job description

About Tiny Health

Tiny Health is advancing lifelong health, from the first 1,000 days to the last, and addressing chronic disease through precision microbiome science. Founded in 2020 and built by microbiome scientists and physicians, our testing platform reveals whether your microbiome is trending toward resilience or imbalances using shotgun metagenomics, proprietary AI, and one of the world's largest longitudinal datasets. Trusted by families and health practitioners alike, our research-backed gut and vaginal tests are redefining the microbiome as a cornerstone of personalized health through every life stage. Learn more at tinyhealth.com and poweredbytiny.com.

The Opportunity

Tiny Health is seeking a Director of Clinical Research to co-own the strategy, execution, and growth of our clinical research program. This role will lead the design and delivery of clinical studies supporting product validation, regulatory strategy, and scientific credibility across our microbiome-based testing and health insights.

As a key scientific leader, you will help build and scale our clinical research infrastructure in a fast-moving, resource-conscious environment, balancing rigor with speed as the program grows.

What You’ll Do

Clinical Strategy & Infrastructure

  • Co-own Tiny Health’s clinical evidence roadmap with the Head of Science

  • Define study objectives, endpoints, and success criteria aligned with product and regulatory goals

  • Build scalable clinical research processes and infrastructure as the company grows

  • Represent Tiny Health in clinical collaborations and external research discussions

Study Design & Execution

  • Lead the design and publication of observational, interventional, and real-world evidence studies

  • Oversee protocol development, statistical analysis plans, and data collection frameworks

  • Manage study timelines, budgets, risk, and regulatory documentation

  • Support regulatory submissions as needed

Cross-Functional & Scientific Communication

  • Partner with Bioinformatics and Engineering to ensure analytical rigor and appropriate data capture

  • Collaborate with Product and Marketing to translate findings into clear, defensible claims

  • Lead study reporting, including reports, abstracts, and peer-reviewed manuscripts

  • Present findings to internal leadership, partners, and scientific audiences

QualificationsRequired
  • PhD, MD, MS/MPH, or equivalent degree in life sciences, clinical research, or a related field

  • 6+ years of experience in clinical research within biotech, diagnostics, digital health, or academia

  • Demonstrated experience designing and executing human clinical studies

  • Hands-on experience with IRB submissions and human subjects research oversight

  • Experience leading cross-functional teams and managing external partners (CROs, academic collaborators, etc.)

  • Strong written and verbal communication skills

  • Experience operating in ambiguity and building scalable systems in early-stage or resource-constrained environments

Preferred
  • Experience supporting regulatory submissions

  • Background in pediatric, maternal-infant, or microbiome-related research

  • Experience generating evidence to support product claims or regulatory strategy

  • Track record of publications in peer-reviewed journals

How we work
  • A mission that actually pulls people in
    We make the microbiome measurable and actionable at every life stage, and real people write in to say it's life-changing.

  • Remote-first, real overlap
    Our FTEs are based in North America and work core hours from 9am–6pm CST, shiftable by up to two hours either way — start at 7am or 11am, wrap at 4pm or 8pm.

  • Written first, huddle second, meet last
    Default to a clear Slack post, huddle when a thread stalls, and meet only to make a real decision.

  • Fast, but never sloppy
    Do the two-month thing in two weeks, then check the work—shipping errors is rework, not speed.

  • Shape what we build, not just how we build it
    There's no playbook waiting for you, so write it—and bring the alternative, not just the objection.

  • Day One mentality
    Fewer titles and layers; process is a guardrail where it counts, never the reason something didn't ship.

  • No hidden agendas
    Numbers, misses, and feedback are shared openly and in real time, so you always know where you stand.

  • High standards, genuinely fun people
    Take the work seriously and ourselves much less—high-performing and fun to be around is the hiring bar.

  • Is this pace for you?
    Venture-scaled and on a steep trajectory, with intensity in spikes, fiercely protected flexibility, and faster growth than anywhere else.

Our Values
  1. Learn Fast, Get Better - Find the root cause, not just the fix, and get better every time

  2. Be Relentlessly Resourceful - Dig for the answer, move fast, and know when to ask for help

  3. Act Like an Owner, Be Hungry to Win - Act like it’s your company, and do whatever it takes to win

  4. Act with Honesty and Empathy - Say what’s true, and say it with care

  5. Delight People by Anticipating Their Needs - Solve the problem, then get two steps ahead of it