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Entry Level Clinical Trial Associate Jobs in Florida

CVAUSA

Sr. Lead Clinical Research Coordinator

Miami, FL · On-site

$70 - $100/hr

Cardiovascular Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care ... As part of our expansion, we are quickly increasing our clinical trial operations and looking for ...

Actalent

Clinical Research Supervisor

Orlando, FL

$95K - $120K/yr

... trial,Project management Additional Skills & Qualifications Bachelor's Degree in Healthcare Administration, Research, or related field and 2 years of experience in clinical research or Associates ...

Actalent

Clinical Research Supervisor

Orlando, FL

$95K - $120K/yr

... trial,Project management Additional Skills & Qualifications Bachelor's Degree in Healthcare Administration, Research, or related field and 2 years of experience in clinical research or Associates ...

usahs

Federal Work Study

Saint Augustine, FL · On-site

$29.25 - $40/hr

General Summary The Federal Work-Study (FWS) Program provides part-time employment to students attending USAHS who need the earnings to help meet their costs of postsecondary education and encourages ...

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Entry Level Clinical Trial Associate information

What is an entry level clinical trial associate?

Entry level clinical trial associates are professionals who support the planning, coordination, and administration of clinical trials, which are research studies conducted to test new medical treatments or drugs. They typically assist with tasks such as data entry, regulatory documentation, trial site communication, and ensuring compliance with study protocols. This role is ideal for individuals starting their careers in clinical research, offering valuable hands-on experience in the field. Entry level clinical trial associates often work under the supervision of clinical trial managers or coordinators and play a crucial role in the success of clinical studies.

What are the typical responsibilities of an entry level clinical trial associate?

As an Entry Level Clinical Trial Associate, your daily tasks often include maintaining clinical trial documentation, assisting with regulatory submissions, and supporting the coordination of study activities. You may also track trial progress, ensure data accuracy, and communicate with study sites to resolve issues or gather missing information. This role is highly collaborative, working closely with clinical research coordinators, project managers, and data management teams to ensure that trials run smoothly and adhere to protocols.

What are the key skills and qualifications needed to thrive as an entry level clinical trial associate?

To thrive as an Entry Level Clinical Trial Associate, you need a bachelor's degree in life sciences or a related field, strong organizational skills, and attention to detail. Familiarity with clinical trial software (such as CTMS), regulatory documentation, and Good Clinical Practice (GCP) guidelines is important. Excellent communication, teamwork, and problem-solving abilities help you effectively support study coordination and interact with cross-functional teams. These skills and qualities ensure accuracy, regulatory compliance, and smooth execution of clinical research projects.

What is the difference between Entry Level Clinical Trial Associate vs Clinical Research Coordinator?

AspectEntry Level Clinical Trial AssociateClinical Research Coordinator
Required CredentialsBachelor's degree, often in life sciences; some certificationsBachelor's degree, often in health sciences; certifications preferred
Work EnvironmentClinical trial sites, pharmaceutical companies, CROsHospitals, clinics, research sites
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, academic institutions, research organizations
Common Search & ComparisonYesYes

The Entry Level Clinical Trial Associate typically supports clinical trials by assisting with data collection, regulatory documentation, and trial logistics. The Clinical Research Coordinator often manages the overall conduct of clinical studies at research sites, including patient recruitment and compliance. While both roles require similar educational backgrounds and certifications, the Associate role is more focused on supporting trial activities, whereas the Coordinator oversees the entire study process at the site level.

What are the most commonly searched types of Entry Level Clinical Trial jobs in Florida?

The most popular types of Entry Level Clinical Trial jobs in Florida are:

What are popular job titles related to Entry Level Clinical Trial Associate jobs in Florida?

For Entry Level Clinical Trial Associate jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Entry Level Clinical Trial Associate jobs in Florida look for?

The top searched job categories for Entry Level Clinical Trial Associate jobs in Florida are:

What cities in Florida are hiring for Entry Level Clinical Trial Associate jobs?

Cities in Florida with the most Entry Level Clinical Trial Associate job openings:

Entry Level Clinical Trial Associate jobs near you
Infographic showing various Entry Level Clinical Trial Associate job openings in Florida as of August 2026, with employment types broken down into 2% As Needed, 77% Full Time, 15% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution.

Clinical Lymphoma Research Associate

Mount Sinai Medical Center

Miami Beach, FL • On-site

Full-time

Medical, Life, Retirement, PTO

Posted 11 days ago

Job description

As Mount Sinai grows, so does our legacy in high-quality health care.
Since 1949, Mount Sinai Medical Center has remained committed to providing access to its diverse community. In delivering an unmatched level of clinical expertise, our medical center is committed to recruiting and training top healthcare workers from across the country. We offer the latest in advanced medicine, technology, and comfort in 12 facilities across Miami-Dade (including our 674-bed main campus facility) and Monroe Counties, with 38 medical services, including cancer care, 24/7 emergency care, orthopedics, cardiovascular care, and more. Mount Sinai takes pride in being South Florida's largest private independent not-for-profit hospital, dedicated to continuing the training of the next generation of medical pioneers.
Culture of Caring: The Sinai Way
Our hardworking, tight-knit community of more than 4,000 dedicated employees fosters an environment of care and compassion. Each member plays a vital role in our collective mission to deliver excellent healthcare through innovation, education, and research. At Mount Sinai, we take pride in our achievements, aiming to be a beacon of quality healthcare in South Florida. We welcome all healthcare professionals to join our thriving community and contribute to our pursuit for clinical excellence.
Department:
Job Description Summary:
Position Responsibilities
  • Serves as the project lead for overseeing the execution of existing lymphoproliferative disorder studies. This includes meeting milestones, troubleshooting, and collaborating with the physician lead, physician extenders, research staff, and industry or academic sponsors of the trials.
  • Establishes an IRB-approved registry to effectively track patients participating in clinical trials and research initiatives.
  • Co-authors manuscripts for submission to peer-reviewed scientific journals using available resources, and assist in developing concepts into protocols.
  • Supports manuscript preparation and abstract presentations for national and international meetings based on current initiatives and clinical trial findings.
  • Collaborates on developing concepts into protocols to implement best practices.
  • Createsan educational outreach platform in partnership with local healthcare providers and community organizations to raise awareness about current research initiatives and clinical trial opportunities.
  • Participates in tumor boards, attend relevant conferences, and join research and service line meetings as directed by the physician lead.
  • Collaborates with the CRC assigned to the protocols to assist with data entry for the tissue registry.
Qualifications
  • License/Registration/Certification
    • Not applicable
  • Education
    • Bachelor's degree in related science.
  • Experience
    • Experience conducting research within a clinical or pre-clinical setting.

Benefits:
We believe in the physical and mental well-being of our employees and are committed to offering comprehensive benefits that fit their personal needs:
  • Health benefits
  • Life insurance
  • Long-term disability coverage
  • Healthcare spending accounts
  • Retirement plan
  • Paid time off
  • Pet Insurance
  • Tuition reimbursement
  • Employee assistance program
  • Wellness program
  • On-site housing for select positions and more!

Degree Requirements:
Certification:

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