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Clinical Data Associate Jobs in Riverview, FL (NOW HIRING)

Alira Health

Clinical Research Associate

Sydney, FL · On-site

Summary ROLE The Clinical Research Associate is an important member of the Alira Health Clinical ... Ensures integrity of CRF data through meticulous and thorough source document review and ...

BayCare

Clinical Research Nurse

Tampa, FL · On-site

Collecting source data for electronic data capture (EDC) systems or Case Report Form (CRF ... Required - Associates in Nursing * Or - Diploma in Nursing * Preferred - Bachelor's in Nursing ...

BayCare

Clinical Research Nurse

Saint Petersburg, FL · On-site

Collecting source data for electronic data capture (EDC) systems or Case Report Form (CRF ... Required - Associates in Nursing * Or - Diploma in Nursing * Preferred - Bachelor's in Nursing ...

Baycare

Clinical Research Nurse

Saint Petersburg, FL · On-site

$70 - $90/hr

Collecting source data for electronic data capture (EDC) systems or Case Report Form (CRF ... Required - Associates in Nursing * Or - Diploma in Nursing * Preferred - Bachelor's in Nursing ...

UAB

RESEARCHER ASSOCIATE

Tampa, FL

Collection of preclinical and clinical imaging data * Perform other duties as assigned. Hourly Range : $ 19.80- $ 25.00 Qualifications Bachelor's degree in a related field OR Associate's degree in a ...

University of Rochester

Social Worker Manager

Tampa, FL · On-site

$66K - $89K/yr

... data, education, experience, qualifications, expertise of the individual, and internal equity considerations. Responsibilities: GENERAL PURPOSE The UCC associate director for clinical services ...

Clear Sight Partners

Ophthalmic Technician

Brandon, FL · On-site

$16.75 - $22.50/hr

They can provide diagnostic information and clinical data in the ophthalmic exam to the physician ... Associates Degree - preferred Skills and Abilities: * Superior interpersonal and communications ...

CLEAR SIGHT PARTNERS

Ophthalmic Technician

Brandon, FL · On-site

$17 - $23/hr

They can provide diagnostic information and clinical data in the ophthalmic exam to the physician ... Associates Degree - preferred Skills and Abilities: * Superior interpersonal and communications ...

CLEAR SIGHT PARTNERS, LLC

Ophthalmic Technician

Brandon, FL · On-site

$17 - $23/hr

They can provide diagnostic information and clinical data in the ophthalmic exam to the physician ... Associates Degree - preferred Skills and Abilities: * Superior interpersonal and communications ...

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All JobsClinical Data Associate JobsClinical Data Associate Jobs in Riverview, FL

Clinical Data Associate information

See Riverview, FL salary details

$12

$34

$77

How much do clinical data associate jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for clinical data associate in Riverview, FL is $34.74, according to ZipRecruiter salary data. Most workers in this role earn between $26.15 and $34.71 per hour, depending on experience, location, and employer.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

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

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

What is the difference between Clinical Data Associate vs Clinical Research Coordinator?

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

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Clinical Data Associate jobs near you

Clinical Research Associate

Sydney, FL • On-site

Alira Health
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Alira Healthexternal

Full-time

Re-posted 27 days ago

Job description

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don't limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.

Job Description Summary

Job Description

ROLE

The Clinical Research Associate is an important member of the Alira Health Clinical team. CRAs are highly motivated and function independently to conduct site monitoring responsibilities for clinical trials. CRAs work closely with the In-house CRAs, Lead CRAs, Director of Clinical Monitoring and Project Managers to ensure sites' protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues.

KEY RESPONSABILITIES

  • Performs qualification, initiation, interim, and close-out visits and ensures proper documentation of site visits.

  • Prepares consistently accurate and timely monitoring visit reports documenting site-related problems, resolutions, actions taken, protocol deviations, study progress, and enrollment status.

  • Facilitates adverse event reporting and ensures the reconciliation of SAE reports with source documentation and CRFs.

  • Ensures integrity of CRF data through meticulous and thorough source document review and verification.

  • Conducts investigational product accountability.

  • Reviews regulatory binder for required documents.

  • Works closely with in-house CRAs and data management to resolve queries on discrepant data.

  • Proactively identifies site issues and develops problem-solving strategies for sites.

  • Maintains regular contact with study sites to ensure protocol/GCP compliance, assesses patient accrual rates, and responds to sponsor requests.

  • Conducts audit preparation at study sites as needed.

  • Works with other CRAs to maintain consistency and promote a collaborative team atmosphere.

  • Manages and resolves conflicting priorities to deliver on commitments.

  • Complies with ICH GCP guidelines, FDA regulations, and company SOPs.

  • Participates in industry and client meetings.

  • Performs additional duties as assigned.

DESIRED QUALIFICATION & EXPERIENCE

  • BS/BA from an undergraduate program or equivalent experience

  • 2 years of clinical research experience

TECHNICAL COMPETENCES & SOFT SKILLS

  • Ability to travel.

  • Proven ability to be careful, thorough, and detail-oriented.

  • Strong organizational skills and the ability to multi-task and work effectively in a fast-paced environment.

  • Self-starter who thrives in a collaborative, yet less structured team environment

  • Ability to problem-solve unstructured or ambiguous challenges.

  • Strong command of English, both written and verbal.

  • Excellent communication and interpersonal skills with customer service orientation.

  • Proficient with MS Office Suite, particularly Word and Excel.

  • Permanent authorization to work in the country where you are applying.

Languages

English

Education

Bachelor of Science (BS): Biology, Bachelor of Science (BS): Life Sciences

Contract Type

Regular

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