Clinical Research Assistant - Core-Ctr For Research Excel

Florida Health Sciences Center Tampa General Hospital

Tampa (FL)

On-site

USD 48,000 - 65,000

Full time

2 days ago

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Job summary

Tampa General Hospital, Inc. is seeking a Clinical Research Assistant to support multiple research projects at the Core Research Center.

The role involves pre-screening participants, obtaining informed consent for registry studies and specific device trials, and coordinating enrollment and visits. You will review lab manuals, collect specimens, and ensure accurate data entry into CRFs while adhering to protocols and privacy requirements.

Qualifications

Bachelor's degree in a science or health care field.
Knowledge of clinical research concepts, regulations, and GCP.
Ability to interpret study protocols and apply inclusion/exclusion criteria.
Understanding of informed consent requirements and ability to explain studies to participants.
Knowledge of specimen collection, processing, labeling and transport per protocol.
Proficiency with EDC/EMR and standard office software (Word, Excel, Outlook).
Strong attention to detail in source documentation and data entry.
Ability to manage multiple studies and meet deadlines in a fast-paced environment.
Strong written and verbal communication for coordination with teams and external contacts.

Responsibilities

Pre-screen potential participants against protocol criteria.
Obtain and document informed consent for registry/observational studies and select devices.
Assist with subject enrollment, randomization, and coordinating research visits.
Review lab manuals and collect/process specimens per protocol.
Enter data from source documents into paper/eCRF and redact when required.
Serve as liaison between research staff and conducting departments.
Support additional tasks as assigned by supervisors and PI.

Skills

Clinical research knowledge

GCP familiarity

Protocol interpretation

Informed consent understanding

EDC/EMR proficiency

Data entry accuracy

Attention to detail

Communication skills

Independence and teamwork

Education

Bachelor's degree in science/health

Tools

Word

Excel

Outlook

EMR/EDC systems

Job description

Job Description - Clinical Research Assistant - Core-Ctr For Research Excel (260004LO)

Job Description

Clinical Research Assistant - Core-Ctr For Research Excel - ( 260004LO )

Description

The Clinical Research Assistant supports multiple clinical research projects under the supervision of the Clinical Research Supervisors and Clinical Research Managers. Key duties include pre-screening potential participants against protocol eligibility criteria; obtaining and documenting informed consent for non-interventional registry/observational studies and select minimal-risk device studies; assisting with subject enrollment, randomization, and coordination of research visits; reviewing study lab manuals and collecting/processing specimens per protocol; performing accurate data entry from source documents to paper/electronic case report forms (including redaction as requested); and serving as a liaison between research staff and departments where research is conducted, along with other assigned tasks.

Qualifications

Bachelor's Degree - Any field related to science or health care
Working knowledge of clinical research concepts, regulations, and Good Clinical Practice (GCP) principles.
Ability to interpret study protocols and apply inclusion/exclusion criteria during pre-screening.
Understanding of informed consent requirements and ability to explain studies to participants in a clear, professional manner.
Working knowledge of specimen collection, processing, labeling, storage, and shipment practices per protocol/lab manual.
Proficiency with electronic data capture (EDC) systems, electronic medical records (EMR), and standard office software (e.g., Word, Excel, Outlook) as applicable to the role.
Strong attention to detail and accuracy in source documentation review, data entry, and record maintenance
Ability to prioritize tasks, manage multiple studies, and meet deadlines in a fast-paced environment.
Effective written and verbal communication skills, including ability to coordinate with multidisciplinary teams and external study contacts.
Professionalism and discretion when handling confidential and protected health information (PHI); ability to follow privacy and security practices.
Problem-solving skills and ability to escape issues appropriately to supervisors/PI/study team.
Ability to work independently with direction, and collaboratively as part of a research team.