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Study Start Up Associate Jobs in Florida (NOW HIRING)

To coordinate the life cycle of the study from start-up through maintenance to closure. * To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and ...

Clinical Research Coordinator

Clearwater, FL

$22.25 - $29.75/hr

Complete all needed activities for study start-up, including completing required training ... A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year ...

Travel CRC

Lake Mary, FL · On-site

$21.25 - $28.25/hr

Complete all needed activities for study start-up, including completing required training ... A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year ...

Complete all needed activities for study start-up, including completing required training ... A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year ...

Clinical Research Coordinator

Maitland, FL · On-site

$22.50 - $30/hr

Complete all needed activities for study start-up, including completing required training ... A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year ...

Travel CRC

Lake Mary, FL · On-site

$21.25 - $28.25/hr

Complete all needed activities for study start-up, including completing required training ... A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year ...

To coordinate and manage the research study lifecycle from start-up through close-out. * To coordinate and conduct all applicable clinical and administrative activities required by the protocol such ...

The ideal candidate would have experience managing clinical research studies from start-up through close-out, overseeing site operations, CRO activities, data collection, investigational product ...

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Showing results 1-20

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 Jul 7, 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:
What cities in Florida are hiring for Study Start Up Associate jobs? Cities in Florida with the most Study Start Up Associate job openings:
CLINICAL RESEARCH NURSE COORDINATOR II (2)

CLINICAL RESEARCH NURSE COORDINATOR II (2)

UAB

Tampa, FL • On-site

$60K - $98K/yr

Other

Posted 27 days ago


UAB Medicine rating

7.4

Company rating: 7.4 out of 10

Based on 185 frontline employees who took The Breakroom Quiz

256th of 877 rated healthcare providers


Job description

The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center is seeking a Clinical Research Nurse Coordinator II.

The O'Neal Comprehensive Cancer Center is one of 51 NCI-designated comprehensive cancer centers in the United States and is the only one in Alabama and in the Deep South region. A comprehensive designation also means UAB Medicine patients have access to leading-edge treatments or clinical trials that they may not otherwise have at local community hospitals or smaller cancer centers. For many, an NCI designation can hold the key to survival. On campus and around Birmingham, the O'Neal Cancer Center is a significant part of our economic powerhouse. The O'Neal Cancer Center powers more than 400 scientists and physician-scientists, cares for 20,000 patients annually, and is home to more than 160 employees, plus all the physicians and clinical staff engaged in cancer patient care. The link to our website is: https://www.uab.edu/onealcancercenter/  

Please attach a current resume with this application.

General Responsibilities

  • To serve as primary coordinator for clinical research studies and supporting more senior team members.

  • To provide a lead role in protocol screening and participant eligibility determination working alongside other team members to ensure compliance. May provide oversight to junior clinical research coordinators (CRC) and clinical research nurse coordinators (CRNC) in review of study documents.

  • To conduct all study activities in accordance with the protocol, Institutional Review Board (IRB) regulations, and Good Clinical Practice (GCP).

  • To provide quality care to participants and their families within the area of clinical specialty.

  • To coordinate the life cycle of the study from start-up through maintenance to closure.

  • To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.

  • To perform the informed consent process following GCP.

  • To act as a liaison between the clinical and research staff, departments, ancillary services and the study sponsor to ensure protocol compliance throughout the study.

Key Duties & Responsibilities

  1. Conducts and understands all study activities in accordance with the protocol, IRB regulations, and Good Clinical Practice (GCP).

  2. Manages the life cycle of the clinical trial from study start-up through trial maintenance to study closure.

  3. Coordinates and organizes patient care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.

  4. Coordinates and organizes clinical patient care provided by a unit.

  5. Follows the patient from referral, consent, screening, through treatment, and follow-up, providing patient and family education and maintaining records and documentation.

  6. Maintains a working nursing knowledge of the department's specialty, drafts documents or policies, collects records, and assists with the preparation of data for publication.

  7. May perform general nursing duties.

  8. Performs other duties as assigned.

Annual Salary Range:    $60,835 - $98,855

Bachelor's degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement. Currently licensed as a Registered Nurse (RN) by the Alabama Board of Nursing required.

Preferences

  • RN, BSN degree.

  • Knowledge of Oncology, clinical research, protocol, and clinical trial management. 

  • Generally, may walk approximately one mile a day and lift 5 pounds daily.

Hard skills: clinical trial, clinical research and data management, protocol compliance management, educating patients and family concerning medical conditions

Soft skills: problem-solving, critical thinking, teamwork, organizational skills, leadership, communication, flexibility, and emotional intelligence.
 

UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.


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