Find & Apply For Clinical Research Coordinator Jobs in Altamonte Springs, Florida

Part-Time Clinical Research Coordinator (CRC) Legacy Research

LLC - 3.7

Altamonte Springs, FL Job Details Part-time $26.66 - $30.00 an hour 1 hour ago Qualifications Research project coordination Clinical data entry Attention to detail Research compliance clinical trial records management CCRP Research participation

Full Job Description Part-Time Clinical Research Coordinator Location:

Altamonte Springs, FL Job Type:

Part-Time Initial Hours:

Approximately up to 20 hours/week during study startup, with opportunity for increased hours after activation and enrollment

Work Location:

On-site About the Position We are seeking an experienced Clinical Research Coordinator (CRC) to join our team on a part-time basis. We are specifically looking for someone who already has hands-on experience coordinating industry-sponsored clinical trials and is comfortable working independently within a small team.

Responsibilities Responsibilities will include:

Assist with study startup and Site Initiation Visit (SIV) preparation Review and understand the study protocol, inclusion/exclusion criteria, and schedule of assessments Assist with regulatory and essential study documentation Coordinate participant recruitment, pre-screening, screening, and study visits Assist with the informed consent process within delegated responsibilities Complete accurate source documentation Enter study data into sponsor EDC systems and respond to queries Obtain and document blood pressure and vital signs according to protocol when trained and delegated Perform Blood Draws, process labs, and coordinate shipments as required Assist with ECGs and other protocol-required assessments when appropriately trained and delegated Maintain screening, enrollment, visit, and study tracking logs Assist with AE/SAE and protocol deviation documentation and escalation Prepare for and participate in sponsor monitoring visits Communicate with the PI, CRA, sponsor, CRO, and study participants Help our team establish efficient study workflows and research processes

Qualifications Required:

Previous hands-on Clinical Research Coordinator or comparable clinical research experience Experience with industry-sponsored clinical trials Experience with source documentation and EDC systems Working knowledge of Good Clinical Practice (GCP) Strong organizational and communication skills Excellent attention to detail Ability to work independently and communicate appropriately with the PI Ability to work on-site in

Altamonte Springs, Florida Preferred:

2+ years of CRC experience Study startup/SIV experience Hypertension, cardiovascular, internal medicine, or primary-care research experience Participant recruitment and enrollment experience Regulatory/IRB experience Experience working with CRAs during monitoring visits Experience obtaining protocol-specific blood pressure measurements, vital signs, and/or ECGs CTMS/eSource experience ACRP or SOCRA certification is a plus but is not required. Schedule & Growth The position will initially require approximately up to 20 hours per week during study startup . Weekly hours may vary depending on study needs. Hours are anticipated to increase following study activation as participant screening, enrollment, and study visits begin. There is potential for continued growth and additional hours as our site enrolls participants and adds future clinical trials. We are looking for an experienced, dependable CRC who is interested in helping a new independent research site successfully launch its first clinical trial and grow its research program.

Pay:

$26.66 - $30.00 per hour Expected hours: 5.0 - 10.0 per week Application Question(s): How many years of hands-on Clinical Research Coordinator experience do you have? Have you previously coordinated an industry-sponsored clinical trial? Are you able to work on-site in Altamonte Springs, Florida, with some flexibility around participant visits and sponsor monitoring visits?

Work Location:

In person