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Study Start Up Associate Jobs in Florida (NOW HIRING)

ARTHREX

Sr. Clinical Study Manager

Naples, FL · On-site

Manages site initiation activities (e.g., study start-up documentation preparation) * Responsible for IRB communication, including document preparation and submission of Arthrex study initiatives.

Arthrex

Sr. Clinical Study Manager

Naples, FL · On-site

Manages site initiation activities (e.g., study start-up documentation preparation) * Responsible for IRB communication, including document preparation and submission of Arthrex study initiatives.

UAB

MANAGER-CLINICAL RESEARCH NURSING

Tampa, FL · On-site

$85K - $139K/yr

To assist with the management of the life cycle of the clinical trial as needed from study start-up through trial maintenance to study closure. * To oversee and/or manage multiple clinical research ...

Barrington James

Site Director

Miami, FL · On-site

$150K - $180K/yr

Support study start-up activities, including staffing, training, feasibility and coordinator assignments. * Develop and support patient/enrollment strategies in collaboration with Principal ...

K2 Staffing LLC

Regulatory Associate

Lady Lake, FL · On-site

The Regulatory Associate is responsible for the development and maintenance of regulatory documents ... The position will manage all aspects of study start-up, modification submissions, ongoing reporting ...

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Study Start Up Associate information

See Florida salary details

$9

$23

$41

How much do study start up associate jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for study start up associate in Florida is $23.57, according to ZipRecruiter salary data. Most workers in this role earn between $15.82 and $31.06 per hour, depending on experience, location, and employer.

What is the difference between Study Start Up Associate vs Clinical Trial Coordinator?

AspectStudy Start Up AssociateClinical Trial Coordinator
Required CredentialsBachelor's degree, knowledge of regulatory requirementsBachelor's degree, familiarity with clinical procedures
Work EnvironmentRegulatory and site initiation activitiesParticipant management and site coordination
Employer & Industry UsagePharmaceuticals, biotech, CROsHospitals, research centers, CROs

The Study Start Up Associate primarily focuses on regulatory submissions, site qualification, and initiation processes, ensuring trial readiness. In contrast, the Clinical Trial Coordinator manages participant recruitment, scheduling, and data collection. Both roles are essential in clinical research but differ in their core responsibilities and focus areas.

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Study Start Up Associate jobs near you
Infographic showing various Study Start Up Associate job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 66% Full Time, 15% Part Time, and 18% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $49,025 per year, or $23.6 per hour.

Clinical Research Site Development Manager/Senior CRC

CENTRAL FLORIDA MEDICAL & CHIROPRACTIC CENTER, INC.

Winter Park, FL • On-site

Full-time

Posted 13 days ago

Job description

Clinical Research Site Development Manager / Senior CRC


Sterling Clinical Research – Central Florida


Sterling Clinical Research is seeking an experienced Clinical Research Site Development Manager / Senior CRC to help grow and manage our expanding clinical research operation.


KEY REQUIREMENT: EXPERIENCE SECURING CLINICAL TRIALS


This is not a traditional CRC position.


We are specifically looking for someone with experience identifying, pursuing, and securing clinical trials from sponsors, pharmaceutical/biotech companies, and CROs.


The ideal candidate understands the full clinical research lifecycle—from study acquisition and feasibility through budget negotiation, site start-up, enrollment, study execution, and closeout.


You Will Have Dedicated Support


You will not be expected to do everything alone.


This position will have a dedicated Assistant CRC to assist with patient scheduling, study coordination, documentation, regulatory tasks, and other day-to-day research activities.


This allows you to focus more heavily on higher-level responsibilities, including bringing new trials to the site, developing sponsor/CRO relationships, negotiating budgets, managing study start-up, and overseeing successful trial execution.


Key Responsibilities


- Identify and pursue new clinical trial opportunities


- Develop and maintain relationships with sponsors and CROs


- Complete feasibility questionnaires and site-selection submissions


- Present our site capabilities to potential sponsors


- Coordinate qualification calls and Site Qualification Visits


- Negotiate study budgets, start-up fees, and other site costs


- Assist with Clinical Trial Agreement (CTA) negotiations


- Manage regulatory and site start-up activities


- Oversee study activation, enrollment, monitoring, and closeout


- Coordinate with investigators, sponsors, CROs, and research staff


- Supervise and work closely with the dedicated Assistant CRC


- Ensure compliance with GCP, FDA, IRB, and protocol requirements


What We’re Looking For


- 3+ years of clinical research experience preferred


- Proven experience obtaining or helping secure clinical trials for a research site


- Experience working directly with sponsors and CROs


- Experience with feasibility questionnaires and site selection


- Experience with study start-up and regulatory processes


- Experience negotiating clinical trial budgets


- Strong knowledge of GCP and clinical research regulations


- Highly organized, proactive, and comfortable taking ownership


- Experience in orthopedics, pain management, spine, neuroscience, or medical device trials is a plus


Why Sterling Clinical Research?


Sterling Clinical Research has something many growing research sites spend years trying to develop:


Patients. Physicians. Facilities. Infrastructure.


Our research operation has access to:


75,000+ patients


13 affiliated medical clinics


Board-certified specialists


Orthopedic, Neurosurgery & Pain Management capabilities


In-house MRI


C-Arm procedure suites and X-ray capabilities


Established patient referral and recruitment infrastructure


Dedicated Assistant CRC support


Our goal is to continue building Sterling Clinical Research into a premier clinical research site in Central Florida.
We already have the infrastructure and patient population. We need an experienced research professional who knows how to turn those capabilities into clinical trial opportunities.
We Especially Want to Hear From You If…
You can confidently say:
“I know how to get clinical trials into a research site.”
When applying, please highlight your experience securing studies, developing sponsor/CRO relationships, negotiating budgets, and launching clinical trials.
Background Screening (Florida): This position requires Level 2 screening through the Florida Care Provider Background Screening Clearinghouse. Learn more: https://info.flclearinghouse.com