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Crc Jobs in Florida (NOW HIRING)

CRC Transportation

Connexion Driver

Jacksonville, FL · On-site

$18/hr

We are seeking dedicated individuals to join CRC Transportation to drive for the Connexion service at JTA In this role, you aren't just driving a vehicle. You'll ensure members of our ADA community ...

CRC TRANSPORT LLC

Warehouse Specialist

Pensacola, FL · On-site

$18 - $29/hr

... at CRC Transport. All Warehouse Specialists operate under the direct supervision and task assignment of the Lead Warehouse. The Warehouse Specialist is the primary executor of daily warehouse ...

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Crc information

See Florida salary details

$7

$21

$35

How much do crc jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for crc in Florida is $21.68, according to ZipRecruiter salary data. Most workers in this role earn between $16.85 and $23.55 per hour, depending on experience, location, and employer.

What is a clinical research coordinator?

Clinical Research Coordinators (CRCs) are professionals who oversee and manage clinical trials and research studies conducted in medical settings. They are responsible for coordinating daily activities, ensuring compliance with protocols, recruiting and enrolling participants, and maintaining accurate records. CRCs work closely with principal investigators, sponsors, and regulatory bodies to ensure that studies are conducted ethically and efficiently. Their role is crucial in advancing medical knowledge and patient care through research.

How does a clinical research coordinator typically collaborate with investigators and study sponsors during a clinical trial?

A Clinical Research Coordinator (CRC) plays a key role in facilitating communication between investigators, study sponsors, and other research staff. CRCs are responsible for ensuring that the study protocol is followed, collecting and managing data, and coordinating patient visits. They often schedule meetings, report progress, handle regulatory documentation, and address queries from sponsors or monitors. This requires strong organizational and interpersonal skills to keep all parties aligned and the study running smoothly.

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

To thrive as a Clinical Research Coordinator, you need a solid background in life sciences, clinical research protocols, and regulatory compliance, often supported by a bachelor's degree in a health-related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as CCRC or ACRP are commonly required. Strong organizational skills, attention to detail, and effective communication help build trust with patients and ensure smooth coordination among research teams. These competencies are crucial for maintaining study integrity, regulatory adherence, and successful trial outcomes.

What is the difference between Crc vs Coder?

AspectCrcCoder
CertificationsCertified Rehabilitation Counselor (CRC) certificationNo specific certification required, but coding certifications like CPC or CCS are common
Work EnvironmentHealthcare, rehabilitation centers, mental health facilitiesHealthcare, medical offices, hospitals, or outpatient clinics
Industry UsageRehabilitation and mental health servicesMedical billing, documentation, and health information management
Job FocusPatient counseling, rehabilitation planningMedical coding, data entry, billing

The main difference between a Crc and a Coder is their focus and certification. Crcs are trained to provide rehabilitation counseling and typically hold specific credentials, working mainly in healthcare and mental health settings. Coders, on the other hand, focus on translating medical records into codes for billing and documentation, often without requiring formal certification. Both roles are essential in healthcare but serve different functions and require different skill sets.

What are the most commonly searched types of Crc jobs in Florida?

The most popular types of Crc jobs in Florida are:

What are popular job titles related to Crc jobs in Florida?

For Crc jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Crc jobs in Florida look for?

The top searched job categories for Crc jobs in Florida are:

What cities in Florida are hiring for Crc jobs?

Cities in Florida with the most Crc job openings:

Crc jobs near you
Infographic showing various Crc job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 20% Part Time, and 1% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $45,099 per year, or $21.7 per hour.

Clinical Research Site Development Manager/Senior CRC

Winter Park, FL • On-site

CENTRAL FLORIDA MEDICAL & CHIROPRACTIC CENTER, INC.
See more jobs at CENTRAL FLORIDA MEDICAL & CHIROPRACTIC CENTER, INC.external

Full-time

Posted 15 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


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