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Crc Research Jobs in Florida (NOW HIRING)

GNP Research

Clinical Research Coordinator

Cooper City, FL

$22.25 - $29.50/hr

GNP Research is seeking an experienced Clinical Research Coordinator (CRC) to lead and manage clinical trials across various therapeutic areas. The ideal candidate is detail-oriented, proactive, and ...

GNP Research

Clinical Research Coordinator

Cooper City, FL

$22.25 - $29.50/hr

GNP Research is seeking an experienced Clinical Research Coordinator (CRC) to lead and manage clinical trials across various therapeutic areas. The ideal candidate is detail-oriented, proactive, and ...

Segal Trials

Clinical Research Coordinator

Lauderhill, FL · On-site

$24 - $32/hr

The CRC plans, coordinates, evaluates, and manages the care of both the participants and the data ... research and coordinate research activities. All duties carried out by the CRC are done in ...

Segal Trials

Clinical Research Coordinator

Hollywood, FL · On-site

$22.25 - $29.50/hr

The CRC plans, coordinates, evaluates, and manages the care of both the participants and the data ... research and coordinate research activities. All duties carried out by the CRC are done in ...

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Crc Research information

See Florida salary details

$9

$28

$57

How much do crc research jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for crc research in Florida is $28.97, according to ZipRecruiter salary data. Most workers in this role earn between $17.62 and $40.79 per hour, depending on experience, location, and employer.

What is a CRC researcher?

CRC Researchers, or Clinical Research Coordinators, are professionals responsible for managing clinical trials and research studies in healthcare settings. Their duties include recruiting and screening participants, ensuring compliance with study protocols, collecting and managing data, and coordinating communication between investigators, sponsors, and participants. CRC Researchers play a vital role in maintaining the integrity and safety of clinical research, contributing to advancements in medical knowledge and patient care.

What skills and qualifications are needed to thrive as a CRC?

To thrive as a Clinical Research Coordinator (CRC), you need knowledge of clinical trial protocols, regulatory compliance, patient recruitment, and typically a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as CCRC or ACRP are highly valued. Strong organizational skills, attention to detail, and effective communication help build rapport with participants and ensure accurate data collection. These competencies are crucial for maintaining ethical standards, data integrity, and the successful execution of clinical studies.

What are common challenges faced by CRC research professionals, and how can they be addressed?

CRC Research professionals often encounter challenges such as recruiting and retaining study participants, ensuring strict adherence to study protocols, and managing extensive regulatory documentation. To address these, it's helpful to develop strong communication skills, maintain organized records, and build rapport with participants. Collaborating closely with investigators, coordinators, and regulatory teams also helps ensure studies stay on track and compliant with all guidelines.

What is the difference between Crc Research vs Crc Technician?

AspectCrc ResearchCrc Technician
CredentialsTypically requires a degree in chemistry, biology, or related fieldOften requires technical certifications or associate degree
Work EnvironmentLaboratory and research settingsFieldwork and laboratory environments
Industry UsageResearch institutions, biotech, pharmaceuticalsManufacturing, quality control, industrial settings

While both roles involve working with CRC (Cyclic Redundancy Check) concepts, Crc Research focuses on scientific investigation and development, often in labs, whereas Crc Technicians handle practical application, testing, and maintenance in industrial environments. The main difference lies in their focus: research versus technical implementation.

What is the role of a CRC Research in research?

A CRC Research typically refers to a Clinical Research Coordinator involved in managing clinical trials, ensuring protocol adherence, recruiting participants, and collecting data. They coordinate between researchers, participants, and regulatory bodies, often requiring knowledge of Good Clinical Practice (GCP) and relevant software tools. Their role is essential for the successful execution and compliance of research studies.

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

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

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

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

Crc Research jobs near you
Infographic showing various Crc Research job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 11% Part Time, and 1% Contract. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution, with an average salary of $60,267 per year, or $29 per hour.

Clinical Research Site Development Manager/Senior CRC

CENTRAL FLORIDA MEDICAL & CHIROPRACTIC CENTER, INC.

Winter Park, FL • On-site

Full-time

Posted 24 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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