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Clinical Study Startup Jobs in Florida (NOW HIRING)

... startup constraints * Translate technical findings into actionable insights for both clinical and ... Experience coordinating studies with external collaborators * Demonstrated success working in ...

Work with clinical team to ensure all needs of students are met * Recruits all teaching staff ... Prepare and implement sequential Math, Science, English and Social Studies Curriculum for all ...

Work with clinical team to ensure all needs of students are met * Recruits all teaching staff ... Prepare and implement sequential Math, Science, English and Social Studies Curriculum for all ...

You'll have the freedom to lead projects and make technical decisions in a startup-speed ... Experience bringing products from bench to commercial launch Background in clinical diagnostics or ...

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Clinical Study Startup information

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$21

$46

$71

How much do clinical study startup jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for clinical study startup in Florida is $46.72, according to ZipRecruiter salary data. Most workers in this role earn between $37.88 and $52.64 per hour, depending on experience, location, and employer.

What is a clinical study startup?

A Clinical Study Startup job involves managing the initial phases of a clinical trial, ensuring all regulatory, ethical, and logistical requirements are met before patient enrollment begins. Responsibilities typically include submitting regulatory documents, coordinating with ethics committees, negotiating contracts, and ensuring trial sites are fully prepared. This role requires strong knowledge of clinical research regulations, timelines, and collaboration with internal and external stakeholders. Effective study startup is crucial for minimizing delays and ensuring compliance with industry standards.

What are the typical responsibilities of someone working in clinical study startup?

Professionals in Clinical Study Startup are primarily responsible for coordinating and executing study initiation activities, including regulatory document collection, ethics submissions, site contracting, and start-up logistics. They work closely with investigators, sponsors, and cross-functional teams to ensure all regulatory and site requirements are met before the clinical trial begins. This role often involves tight deadlines and frequent communication with stakeholders both internally and externally. It's a fast-paced position that is ideal for individuals who enjoy detail-oriented work and project coordination in a collaborative environment.

What are the key skills and qualifications needed to thrive in clinical study startup, and why are they important?

Success in a Clinical Study Startup role requires a strong understanding of clinical research processes, regulatory requirements, project management, and often a life sciences degree or related field. Familiarity with clinical trial management systems (CTMS), electronic trial master files (eTMF), and regulatory submission platforms is essential, along with certifications like GCP (Good Clinical Practice) being advantageous. Attention to detail, proactive problem-solving, and excellent organizational and communication skills help candidates excel. These qualifications ensure smooth study initiation, regulatory compliance, and effective cross-functional collaboration within demanding timelines.

What are the most commonly searched types of Clinical Study Startup jobs in Florida?

The most popular types of Clinical Study Startup jobs in Florida are:

Infographic showing various Clinical Study Startup job openings in Florida as of August 2026, with employment types broken down into 2% As Needed, 77% Full Time, 15% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $97,174 per year, or $46.7 per hour.
Kalogon, Inc.
Medical Equipment and Supplies Manufacturing • 11 - 50 employees

$60K - $120K/yr

Full-time

Retirement, PTO

Re-posted 8 days ago


Job description

As Kalogon's Research Lead, you'll architect and oversee our research ecosystem, ensuring methodological rigor as you manage a range from quick and dirty user testing to consumer surveys to clinical validation. You'll be conducting in-house research and working with outside groups to go a level deeper.

This role blends strategic vision with hands-on execution, requiring equal expertise in clinical seating assessments and cross-functional collaboration to translate insights into tangible advancements.

Key Responsibilities
  • Use a variety of research modalities to answer key questions about seating from comfort surveys to blood flow analysis and everything in-between
  • Balance long-horizon clinical validation with short-term product development needs
  • Conduct user research, beta testing, and claims research
  • Socialize research findings and ensure team members can self-support by creating tools to access your research
  • Write, field, and analyze consumer surveys on seating, sitting, or any topic as discussed with the team
  • Help drive the business by ideating, testing, and validating unique claims that can be published or shared publicly
  • Support partner by gathering key stakeholder and end user feedback, synthesizing this and sharing insights with the team
  • Work with sales, product, and marketing for post-market surveillance activities
  • Identify and establish relationships with potential research partners including clinics, universities, and rehabilitation centers
  • Handle all research activities from project design through recruitment to final analysis
  • Run beta testing programs 
  • Develop and execute IRB protocols 
  • Manage project timelines and resource needs within startup constraints
  • Translate technical findings into actionable insights for both clinical and non-clinical folks
  • Stay abreast of key research happening in seating and sitting, ensuring the team is aware and taking this research into their work
Qualifications
  • Master's degree or higher in rehabilitation science, biomedical engineering, clinical research, life sciences, or related field
  • Hands-on experience with a wide variety of user research methodologies and quick-turn usability testing
  • Ability to write effective research plans, protocols, interview guides and the like
  • Great understanding of statistics or qualitative insights and what is meaningful in research results
  • Experience managing clinical research projects with minimal supervision
  • Ability to navigate IRB processes efficiently
  • Experience coordinating studies with external collaborators
  • Demonstrated success working in resource-constrained environments
  • Self-starter mentality with exceptional time management skills
  • Ability to communicate effectively with diverse stakeholders 
  • Experience with data analysis tools and research documentation
  • Understanding of regulatory requirements for medical devices at a startup scale
Must-Have Traits
  • Creative problem-solver who can determine the right research approach for the desired outcomes
  • Adept at creating strong internal relationships
  • Comfortable with ambiguity and changing priorities
  • People skills to engage potential research participants and partners
  • Ability to independently prioritize research needs without extensive guidance
  • Passion for both scientific validity and practical application
  • Comfort switching between deeply technical and highly accessible communication
  • Enthusiasm for the startup journey including its challenges and rewards
  • Willingness to travel
Nice-to-Have Experience
  • Previous work in early-stage startups
  • Established connections in clinical rehabilitation settings
  • Experience developing research protocols with limited resources
  • Background in both clinical and commercial product testing
  • History of successful grant writing to fund research initiatives
  • Connections within rehabilitation clinical communities
  • Know something about seating, sitting, or butts or wants to learn
$60,000 - $120,000 a year
This role is based in Melbourne, Florida at Kalogon HQ.

Kalogon offers a competitive salary and benefits package.

Other benefits include:

  • Equity
  • 401k with matching
  • 20 days off per year 
  • 5 all-team holidays, 3 floating holidays* (floating holidays depend on hire date)

*Number of floating holidays and PTO vary based on start date during year.
Kalogon is an E-Verify employer.
People with disabilities are encouraged to apply. If you require a disability-related accommodation for your application, please email us at [email protected].

About Kalogon

Kalogon is the trusted leader in seated health, delivering inventive seating solutions that eliminate the stresses of sitting. Driven by clinical research, deep customer empathy and rapid product iterations, Kalogon's solutions serve anyone who sits for extended periods, across healthcare, aviation and beyond. 

Founded in 2019 and headquartered in Melbourne, Fla., Kalogon has been recognized for our work by CES, TIME, Forbes, Digital Health, among others.

Our team is a blend of experienced tech industry veterans, passionate engineers, and people focused on ways to help folks stay seated and stay healthy. Learn more at www.kalogon.com.

Learn more at www.kalogon.com/careers

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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