Clinical Research Coordinator II

The Clinical Research Coordinator is responsible for supporting the management and oversight of clinical trials. This role involves working closely with a team to ensure the smooth execution of research studies under the guidance of the Site Operations Manager.

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\n Essential Functions

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• :Overseeing Clinical Trial
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• sEnsure trouble-free running of clinical trials
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• .Monitor study participants’ health throughout the trial
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• .Compile reports summarizing the success or failure of drugs, technologies, or medical procedures
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• .Oversee 3-4 trial
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sData Collection and Analysis

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• :Collect data obtained from research
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• .Analyze research data
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.Participant Interaction

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• :Communicate with study participants regarding study objectives
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• .Administer questionnaires
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• .Monitor participant adherence to study rules
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.Collaboration and Compliance

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• :Liaise with laboratorie
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• sMonitor study compliance with protocols and ethical standards
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• .Ensure adherence to regulatory requirements
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.Record Keeping

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• :Maintain research records, including case report forms and drug dispensation records
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• .Direct specimen collection, labeling, storage, and transport
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.Logistics and Supplies

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• :Ensure all necessary equipment and supplies are in stock and functional
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.Education/Experience/Skills

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  \n Education: Bachelor's degree preferred in health-related fie
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ldExperience: 2-year experience in Clinical Research:

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-Must have at least 2 years of experience working on-site directly with patient

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• s!Must have study start up, enrollment, and closeout experienc
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e.
\n Skills Regulat

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• oryFiling and accessing documents, Study Submission Assist
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antFina

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• nceStipend payme
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ntsSubject Interact

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• ionRecruit, interview, screen, enroll, and randomize subje
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• ctsObtain Informed Cons
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• entCollect medical hist
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• oryConduct study vis
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• itsAdministrative Source documentat
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• ion
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• EDCQuery resolut
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• ionAE/SAE documentation and report
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• ingAddress protocol deviati
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• onsOrder suppl
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iesClinical Ski

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• llsPhlebot
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• omyVital Si
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• gns
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ECG