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Study Start Up Associate Jobs in Florida (NOW HIRING)

Alcanza

Lab Coordinator/ Phlebotomist

Largo, FL · On-site

$14.50 - $18.25/hr

... for new study start-up * Transport samples * Provide mentoring to new hires and allow them to ... Associates degree is preferred. Bilingual (English/Spanish) skills are a plus. Required Skills:

BayCare Health System

Clinical Research Coordinator

Tampa, FL · On-site

$23 - $30.50/hr

Ensure study start-up completion worksheet is complete with required protocol specific training of ... Or - 2 years of research experience with an Associates Degree in related field and CRC (Clinical ...

BayCare Health System

Clinical Research Coordinator

Tampa, FL · On-site

$23 - $30.50/hr

Ensure study start-up completion worksheet is complete with required protocol specific training of ... Or - 2 years of research experience with an Associates Degree in related field and CRC (Clinical ...

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Study Start Up Associate information

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

As of Aug 9, 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.

What are popular job titles related to Study Start Up Associate jobs in Florida? For Study Start Up Associate jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Study Start Up Associate jobs in Florida look for? The top searched job categories for Study Start Up Associate jobs in Florida are:
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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, 64% Full Time, 16% Part Time, 1% Temporary, 17% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $49,025 per year, or $23.6 per hour.

Clinical Research Assistant/Pharmacy Tech

Cardiovascular Associates of America

Daytona Beach, FL • On-site

Full-time

Posted 20 days ago

Job description

Clinical Research Assistant 
This will be an in-person position in Daytona Beach (Hybrid)

Position Summary 

The Clinical Research Assistant (CRA) provides operational and participant support for clinical research studies conducted at the site. This position assists Clinical Research Coordinators (CRCs), investigators, and study teams with participant scheduling, specimen processing, investigational product accountability support, supply management, and study-related documentation. 

The Clinical Research Assistant plays a critical role in ensuring efficient study conduct while allowing coordinators to focus on protocol management, participant care, and study execution. 

Essential Responsibilities 

Participant Support and Scheduling 

  • Coordinate participant appointments and study visits. 

  • Contact participants regarding upcoming visits and study requirements. 

  • Assist with visit preparation and participant flow. 

  • Maintain study calendars and visit schedules. 

  • Support participant retention activities. 

Study Operations 

  • Maintain research supplies and study materials. 

  • Order study-related supplies and equipment as directed. 

  • Monitor inventory levels and maintain adequate stock. 

  • Track expiration dates of study supplies and research materials. 

  • Ensure study materials are organized and readily available. 

Specimen Processing and Shipping 

  • Process biological specimens according to protocol requirements. 

  • Prepare and package specimens for shipment. 

  • Complete shipping documentation and laboratory requisitions. 

  • Maintain specimen shipment records. 

  • Coordinate with central laboratories and couriers. 

Study Documentation and Logs 

  • Maintain temperature logs and equipment monitoring records. 

  • Maintain medication accountability logs and inventory documentation. 

  • Assist with essential study documentation. 

  • Ensure logs are completed, accurate, and up to date. 

  • Support filing and organization of study records. 

Regulatory and Administrative Support 

  • Assist with document collection and filing. 

  • Route study documents for review and signature. 

  • Support maintenance of regulatory binders and electronic regulatory systems. 

  • Assist with study start-up and close-out activities. 

Quality and Compliance 

  • Follow protocol requirements, GCP, sponsor requirements, and site SOPs. 

  • Escalate protocol deviations, equipment issues, or documentation concerns. 

  • Participate in training and quality improvement activities. 

  • Maintain confidentiality of participant and study information. 

Qualifications 

Education 

  • High School Diploma required. 

  • Associate's or Bachelor's degree in a health science, biological science, or related field preferred. 

Experience 

  • Current or previous Pharmacy Technician experience is required

  • Experience handling specimens or laboratory procedures preferred. 

Knowledge, Skills, and Abilities 

  • Strong organizational skills. 

  • Ability to manage multiple priorities. 

  • Attention to detail and accuracy. 

  • Strong communication and customer service skills. 

  • Ability to work independently and within a team environment. 

  • Proficiency with Microsoft Office applications. 

  • Ability to learn CTMS, EDC, and sponsor systems. 

Physical Requirements 

  • Ability to stand, walk, and move throughout clinical areas. 

  • Ability to lift and transport study supplies and specimen shipments up to 25 pounds. 

  • Ability to perform repetitive computer-based tasks. 

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