Clinical Research Assistant - Core-Ctr For Research Excel

''685404'',''true'',''685404'',''false'',''Submission for the position: Clinical Research Assistant - Core-Ctr For Research Excel - (Job Number: 260003WI)'',''false'',''685404'',''false'',''true'',''Clinical Research Assistant - Core-Ctr For Research Excel'',''260003WI'',''!*!

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.

'',''!*!

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.

'',''!*!

• 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 escalate issues appropriately to supervisors/PI/study team.
• Ability to work independently with direction, and collaboratively as part of a research team.

'',''!*!

• 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 escalate issues appropriately to supervisors/PI/study team.
• Ability to work independently with direction, and collaboratively as part of a research team.

'',''Tampa'',''Tampa'','''','''',''

TGH Main Campus (TGHMAIN)

1 Tampa General Circle

Tampa, 33601

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